USE OF ALPHAVIRUS IN PREPARATION OF ANTITUMOR DRUGS

Abstract

Disclosed is use of alphavirus in preparation of antitumor drugs. The alphavirus is M1 virus or Getah virus. In addition, the specific tumor types sensitive to abovementioned alphavirus treatment are further determined, so as to provide a safe and effective solution for antitumor drug administering schemes.

Claims

1-10. (canceled)

11. A method of treating a subject, preferably a human subject with tumor, comprising administering to the subject at least one alphavirus, wherein said alphavirus is selected from an M1 virus and a Getah virus.

12. The method of claim 11, wherein the tumor is a ZAP low expression tumor or ZAP negative tumor.

13. The method of claim 11, wherein the tumor is a solid tumor with ZAP low expression or a ZAP negative solid tumor.

14. The method of claim 11, wherein the tumor is liver cancer, colorectal cancer, bladder cancer, breast cancer, cervical cancer, prostate cancer, glioma, melanoma, pancreatic cancer, nasopharyngeal carcinoma, lung cancer, or gastric cancer.

15. The method of claim 11, wherein the tumor is ZAP low expression or ZAP negative tumor selected from liver cancer, colorectal cancer, bladder cancer, breast cancer, cervical cancer, prostate cancer, glioma, melanoma, pancreatic cancer, nasopharyngeal carcinoma, lung cancer, and gastric cancer.

16. The method of claim 11, wherein the alphavirus is administrated by injection or orally, preferably, by injection; preferably, the alphavirus is administrated by intravenous injection or intratumoral injection; more preferably, a) in the intratumoral injection, 2×10.sup.5 PFU/kg-2×10.sup.9 PFU/kg is administrated every day; or, b) in the intravenous injection, 2×10.sup.6 PFU/kg-2×10.sup.10 PFU/kg is administrated every day.

17. An antitumor administrating system, comprising a ZAP expression level detecting reagent and at least one alphavirus, wherein the alphavirus is selected from an M1 virus and a Getah virus.

18. An antitumor medicament, comprising at least one alphavirus and ZAP inhibitor(s), wherein the alphavirus is selected from an M1 virus and a Getah virus.

19. The medicaments of claim 18, wherein the ZAP inhibitor is a tumor targeted ZAP inhibitor.

20. The method of claim 11, wherein said alphavirus is selectively enriched in tumor tissue after administration.

21. The method of claim 11, wherein a ZAP inhibitor is also administrated during or prior to the administration of said alphavirus; preferably, the ZAP inhibitor is a tumor targeted ZAP inhibitor.

22. The method of claim 21, wherein the ZAP inhibitor is selected from ZAP expression inhibitor and function inhibitor.

23. The method of claim 21, wherein the ZAP inhibitor is selected from ZAP interference fragment and ZAP antibody.

24. The method of claim 11, wherein before administrating, the subject is subjected to the detection of tumor ZAP expression level, and, a) if the tumor is of ZAP low expression or ZAP negative expression, said alphavirus is directly administrated; b) if the tumor is of ZAP normal expression/ZAP high expression, a ZAP inhibitor is provided before or during the administration of the M1 virus.

25. The method of claim 24, wherein the ZAP inhibitor is a tumor targeted ZAP inhibitor.

26. The method of claim 11, wherein the genome of said at least one alphavirus has at least 97.8% nucleotide sequence identity to the genome of the M1 virus deposited under Accession No. CCTCC V201423.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0044] FIG. 1 shows that M1 virus significantly causes cytopathic effect of the tumors;

[0045] a) shows that M1 virus infection causes cytomorphological change of the tumors;

[0046] b) shows that M1 virus infection has no effect on morphology of normal cell lines, Control represents a control group of OptiPRO™ SFM medium, M1 represents an experiment group of M1 virus infection.

[0047] FIG. 2 shows that M1 virus effectively inhibits tumor growth of a tumor-bearing mice;

[0048] a) shows the influence of M1 virus on the tumor volume and animal body weight of a Hep3B tumor-bearing mice after treated with intratumoral injection of M1, wherein M1 represents M1 virus treated group, solvent represents a control group of OptiPRO™ SFM medium solvent, (n=9);

[0049] b) shows influence of M1 virus on tumor volume and animal body weight of a LoVo tumor-bearing mice after treated with intratumoral injection of M1, (n=11);

[0050] c) shows influence of M1 virus on tumor volume and animal body weight of Hep3B tumor-bearing mice after treated with intravenous injection of M1, (n=9);

[0051] d) shows tissue distribution of M1 in the Hep3B tumor-bearing mice after treated with intravenous injection of the M1 virus. QRT-PCR detection is conducted (n=6);

[0052] The data of the tumor volume and body weight are represented by mean value±standard deviation, and the statistical method is ANOVA method; the arrows represent for M1 virus treated group, the circles represent for the control group of OptiPRO™ SFM medium, ns represents for no statistical difference; i.t represents for intratumoral injection, i.v represent for intravenous injection; and * represents that on mRNA expression of M1 virus is detected.

[0053] FIG. 3 shows that M1 virus selectively causes cell death of ZAP low expression/ZAP negative tumors;

[0054] a) shows differential expression of ZAP mRNA expression quantity in different cells; and ND represents that mRNA expression of ZAP is not detected;

[0055] b) shows differential expression of ZAP protein expression quantity in different cells; and β-actin is an internal reference;

[0056] c) shows the ZAP protein level in cells and the change of cell survival rate caused by the M1 virus infection. β-actin is the internal reference. statistical analysis of student's test is conducted. ** P<0.01;

[0057] d) shows that for normal cell L-02, tumor cell PLC and HCT116, after the knockdown of ZAP, cell death was induced significantly by M1 virus. The hollow circles/hollow triangles/hollow inverted triangles represent for the groups with interference knockdown of ZAP, the solid circles/solid triangles/solid inverted triangles represent for the groups of negative control of messy code interference. Students't test was adopted for statistical analysis, */#/& represents for P<0.05, & & represents for P<0.01, and ns represents for no statistical difference;

[0058] e) shows that for normal cell L-02, tumor cell PLC and HCT116, after the knockdown of ZAP, relative titer of the M1 virus is increased. Students't test was adopted for statistical analysis, and * represents for P<0.05;

[0059] f) shows that for normal cell L-02, tumor cell PLC and HCT116, after the knockdown of ZAP, the M1 virus RNA expression is increased. Students't test was adopted for statistical analysis, * represents for P<0.05, and ** represents for P<0.01;

[0060] g) shows that for normal cell L-02, tumor cell PLC and HCT116, after the knockdown of ZAP, the M1 virus protein NS3 and E1 expression are increased. GAPDH is used as the internal reference;

[0061] h) shows that an overexpresssion of ZAP partially block tumor cell death caused by M1 virus. Students't test was adopted for statistical analysis. # represents for P<0.05, and ns represents for no statistical difference;

[0062] i) shows that for tumor cells with an overexpression of ZAP, the relative titer of M1 virus is reduced. Students't test was adopted for statistical analysis. ** represents for P<0.01;

[0063] j) shows that for tumor cells with an overexpression of ZAP, the M1 virus RNA is reduced. Students't test was adopted for statistical analysis. ** represents for P<0.01;

[0064] k) shows that for tumor cells with an overexpression of ZAP, the expression of protein NS3 and E1 of the M1 virus is increased. β-actin is used as the internal reference.

[0065] FIG. 4 shows that the inhibition rate of M1 virus against human ex vivo living tumor tissue is negatively correlated with ZAP mRNA expression level; ZAP mRNA expression is determined by QRT-PCR. The ZAP relative expression quantity of the M1 virus ineffective group (inhibition rate ≦10%) is compared with that of M1 virus effective group (inhibition rate >10%). For those tumor tissues in which the inhibition rate of M1 virus treatment is less than or equal to 10%, the median of the ZAP normalized expression quantity is 0.414. For those tumor tissues in which the inhibition rate of M1 virus treatment is more than 10%, the median of the ZAP expression quantity is 0.075. Rank-sum test was adopted for statistical analysis adopts, P<0.05.

[0066] FIG. 5 shows a low expression of ZAP in various types of clinical pathological tumor tissues;

[0067] a) shows expressions of ZAP in clinical pathological tumor tissues by imunohistochemical staining detection; N: paracancerous non-neoplastic group, T: tumor group;

[0068] b) shows that in various types of tumor clinical pathological tissues, the ZAP expression in the tumor group is significantly lower than that in the paracancerous non-neoplastic group; N: the paracancerous non-neoplastic group, T: the tumor group; N and T adopt rank-sum test was adopted for statistical analysis, *** P<0.001;

[0069] c) shows that in various types of clinical pathological tumor tissues, the ZAP expression of the tumor tissues is lower than that in the paracancerous non-neoplastic tissues.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0070] The present disclosure is further illustrated by the following embodiments. However, embodiments of the present disclosure are not limited to the following description of the examples. Equivalent changes or adaptations made according to the principle or idea of the present disclosure should be deemed as within the protection scope of the present invention.

[0071] The materials and experiment methods used in the present disclosure are conventional materials and methods, unless otherwise specified.

Example 1. M1 Virus Selectively Caused Tumor Cells Death

[0072] 1) M1 Virus Significantly Causes Morphological Change of Tumor Cell

[0073] Materials:

[0074] Hepatocellular carcinoma Hep3B, human bladder transitional cell carcinoma T24, human colorectal cancer LoVo, human immortalized normal liver cell line L-02, M1 virus, high glucose DMEM medium, F-12 medium, inverted phase contrast microscope.

[0075] Methods:

[0076] a) Cultivation of cells: human hepatocellular carcinoma cell line Hep3B, human bladder transitional cell carcinoma cell line T24, and human immortalized normal liver cell line L-02 were grown in a DMEM complete medium containing 10% FBS, 100 U/ml penicillin and 0.1 mg/ml streptomycin; the human colorectal cancer cell line LoVo was grown in a F-12 complete medium containing 10% FBS, 100 U/ml penicillin and 0.1 mg/ml streptomycin. The cell lines were all placed in a 5% CO.sub.2, 37□ constant temperature closed incubator (relative humidity 95%) for subculture. Growth of the cell lines was observed with the inverted microscope. Cells are passaged about every 2-3 days, and the cells in exponential growth phase were extracted for a formal experiment.

[0077] b) Observation under the cell microscope: the cells in exponential growth phase were selected, and added into a DMEM or F-12 complete medium (containing 10% fetal bovine serum, 1% double antibody) to prepare a cell suspension. The cells were inoculated into a 24-well culture plate at a density of 2.5×10.sup.4/well. After 48 hours from the infection treatment with M1 virus (MOI=1), cytomorphological changes were observed under the inverted phase contrast microscope.

[0078] Results:

[0079] The cytomorphology was observed under the phase-contrast microscope. Hep3B cell, T24 cell and LoVo cell were all of adherent monoculture growth, and the cells were closely arranged, and the phenotypes were uniform. However, after 48 hours from the M1 virus (MOI=1) treatment, the morphology of the cells were obviously altered. Compared with the cells in the control group, the cell number in the viral infection group was obviously deceased. The cell body was contracted to a spherical shape, and its refractive index was obviously increased, presenting a death pathological change, as shown in FIG. 1a. FIG. 1b shows effect of the M1 virus infection on the normal cells. L-02 cells were infected by M1 virus with the equal titer, and no obvious change in cell number and morphology was found. The results indicate that M1 virus selectively caused cell death of tumor cells, but had no effect on the survival of the normal cells.

[0080] 2) M1 Virus Selectively Reduced Survival of the Tumor Cell Lines

[0081] Materials:

[0082] Thirty four tumor cell lines (see Table 1), three human immortalized normal cell lines (see Table 1), M1 virus, high glucose DMEM medium, F-12 medium, MTT (tetramethyl thiazolyl tetrazolium).

[0083] Methods:

[0084] a) Inoculation of cells and administration treatment: the cells in the exponential growth phase were selected and added into the DMEM (or F-12) complete medium (containing 10% fetal bovine serum and 1% double antibody) to prepare a cell suspension, and inoculated into a 96-well culture plate at a density of 4×10.sup.3/well. After 12 hours the cells were found completely adherent to the wall. The experiment was divided into an experiment group and a control group, the experiment group was M1 virus (MOI=10) infected cell; the control group was high glucose DMEM solvent control group. Five composite orifices were disposed in the two groups.

[0085] b) Reaction of MTT with succinate dehydrogenase in the cells: when cultured to 48 hours, MTT 15 μl (5 mg/ml) was added into each well, and the incubation was continued for 4 hours. By microscopic examination, granular blue and purple formazan crystal formed in the living cells were observed.

[0086] c) Dissolution of formazan particles: the supernatant was carefully sucked off, and DMSO 100 μl/well was added to dissolve the resulting crystal, then the resulting solvent was shook on a microoscillator for 5 minutes, and the optical density (OD value) of each well was detected on a enzyme linked detector at a wavelength of 570 nm. The experiments were repeated for 3 times in every group. Cell survival rate=OD value of drug treatment group/OD value of control group×100%.

[0087] Results:

[0088] As shown in Table 1, after 48 hours of tumor cell treatment with M1 virus (MOI=10), the cell death rate of pancreatic cancer, nasopharyngeal carcinoma, prostate cancer and melanoma were more than 50%; the cell death rate of colorectal cancer (LoVo, HCT-8, SW620 and SW480), liver cancer (Hep3B, Huh-7 and Huh-6), bladder cancer and breast cancer were more than 40%; the cell death rate of glioma, cervical cancer, lung cancer were more than 30%; the cell death rate of gastric cancer was more than 20%. There were no statistically significant changes in the cell survival rate of three normal cell lines (L-02, HEB and SV-HUC-1) as well as PLC and HCT116. The results indicated that the M1 virus infection selectively caused cell death in most of the tumors.

TABLE-US-00001 TABLE 1 M1 virus significantly reduced survival rate of tumor cells Survival rate Statistical Cell lines Source (%) significance Hep3B Liver cancer  3.8 — Huh-7 Liver cancer  52.2 ± 10.0 ** Huh-6 Liver cancer 59.0 ± 8.9 ** Hep G2 Liver cancer 70.4 ± 3.5 * PLC Liver cancer 80.5 — HCT116 Liver cancer 81.3 ± 4.3 ns LoVo Colorectal cancer  6.9 — HCT-8 Colorectal cancer 35.4 ± 5.2 ** SW620 Colorectal 43.7 ± 6.7 ** adenocarcinoma SW480 Colorectal cancer 53.8 ± 8.4 ** SCaBER Bladder cancer 11.5 ± 4.4 ** T24 Bladder cancer 21.1 ± 3.8 ** UM-UC-3 Bladder cancer  39.8 ± 19.6 ** 5637 Bladder cancer  50.2 ± 19.0 ** Capan-1 Pancreatic cancer  40.4 ± 10.1 ** PANC-1 Pancreatic cancer  49.3 ± 16.3 ** SW1990 Pancreatic cancer  45.6 ± 16.9 ** MIA PaCa-2 Pancreatic cancer  49.1 ± 13.2 ** U-87 MG Malignant glioma 32.4 — U-251 Malignant glioma 34.7 ± 4.9 ** T98G Glioblastoma 38.2 — multiforme U-138 MG Malignant glioma 40.1 — MGR2 Glioma 63.2 — MDA-MB-468 Breast cancer  43.7 ± 10.1 ** MDA-MB-231 Breast cancer 58.9 ± 2.7 ** C-33 A Cervical cancer 14.8 ± 1.8 ** HeLa Cervical cancer 66   — 22Rv1 Prostate cancer 39.1 — CNE-2 Nasopharyngeal 24.5 — carcinoma CNE-1 Nasopharyngeal 48.2 — carcinoma A-375 Melanoma  47.3 ± 19.2 * A549 Lung cancer 68.2 — NCI-N87 Gastric cancer 76.4 ± 9.3 * HGC-27 Gastric cancer 79.2 — L-02 Normal liver cell 100.3 ± 10.0 ns HEB Glial cell 98.8 — SV-HUC-1 Oviductal epithelial 97.2 — immortalized cell (Note: ** p < 0.01, * p < 0.05, ns: the difference has no statistical significance. Statistical methods: student's test, — : no statistics).

Example 2. M1 Virus Selectively and Effectively Inhibited Tumor Growth

[0089] 1) In Tumor-Bearing Mice Body, M1 Virus Effectively Inhibiting Tumor Growth

[0090] Materials:

[0091] M1 virus, human liver cancer cell line Hep3B, human colorectal cancer cell line LoVo, fifty eight 4-week-old female BALB/c nude mice.

[0092] Methods:

[0093] a) Modeling of the tumor-bearing mice: 5×10.sup.6Hep3B or LoVo cells were dorsal subcutaneously injected into 4-week-old BALB/c nude mouse.

[0094] b) Intratumoral administration: when Hep3B tumor volume reached about 50 mm.sup.3 or LoVo tumor volume reached about 70 mm.sup.3, the intratumoral injection administration was initiated. The tumor was injected with M1 viruses for totally six times within 12 days (2×10.sup.6 PFU/time), and OptiPRO™ SFM medium injection treatment was set as solvent control group. Length and width of the tumor and body weight were measured every two days, and the volume of the tumor was calculated according to the formula: length×width.sup.2/2.

[0095] c) Intravenous administration: when Hep3B cell tumor volume reached about 50 mm.sup.3, it was intravenously injected with M1 virus (3×10.sup.7 PFU/time), and after three days, a second intravenous injection was administrated. OptiPRO™ SFM medium injection treatment was set as the solvent control group. The body weight and length and width of the tumor were measured every three days, and the volume of tumor was calculated according to the formula: length×width.sup.2/2.

[0096] Results:

[0097] After subcutaneous tumor-bearing Hep3B (FIGS. 2a and 2c) and LoVo (FIG. 2b) nude mouse models were established on the BALB/c nude mouse, M1 viruses were administrated continuously for several times by intratumoral (FIG. 2a and FIG. 2b) or intravenous injection (FIG. 2c), and the changes of tumor volume and animal body weight of the nude mouse were observed. In the Hep3B nude mouse model, intratumoral injection administration was adopted as shown in FIG. 2a. At the 20.sup.th day the experiment was terminated, the mean value of tumor volume of the solvent control group was 0.368±0.051 cm.sup.3, and the mean value of tumor volume of the M1 virus group was 0.172±0.058 cm.sup.3. Statistic results indicated that M1 virus significantly inhibited tumor growth of the Hep3B tumor-bearing mice. In addition, there is no significant difference in average body weight between the M1 virus group nude mouse (16.4±1.54 g) and the control group nude mouse (17.0±1.16 g), and the mental status of the M1 virus group nude mouse were good, indicating a good safety of the M1 virus. In the LoVo nude mouse model, intratumoral administration was conducted as shown in FIG. 2b. The experiment was terminated at the 24.sup.th day, the mean value of tumor volume in the control group was 0.546±0.087 cm.sup.3, and the mean value of tumor volume in the M1 virus group was 0.389±0.049 cm.sup.3. Statistic results indicated that M1 virus significantly inhibited tumor growth of the LoVo tumor-bearing mice. In addition, there is no significant difference in average body weigh between M1 virus group nude mouse (18.9±1.40 g) and the control group nude mouse (19.4±1.86 g), and the mental status were good, indicating a good safety of the M1 virus; in the Hep3B nude mouse model, intravenous injection administration was conducted as shown in FIG. 2c. The experiment was terminated at the 21.sup.st day, the average tumor volume of the control group was 0.247±0.067 cm.sup.3, and the average tumor volume in the M1 virus group was 0.134±0.057 cm.sup.3. Statistic results indicated that M1 virus significantly inhibited tumor growth of Hep3B tumor-bearing mice. In addition, there is no significant difference in average body weight between the M1 virus group nude mouse (17.2±2.50 g) and control group (17.5±2.16 g), and the mental status were good, indicating a good safety of the M1 virus.

[0098] 2) M1 Virus was Selectively Enriched in the Tumor Tissue

[0099] Materials:

[0100] Twenty four 4-week old female BALB/c nude mice, liver cancer cell line Hep3B, Trizol, a tissue homogenizer, a real-time fluorescence quantitative PCR instrument.

[0101] β-Actin Primer:

TABLE-US-00002 Sense strand (SEQ ID No. 1: GATCATTGCTCCTCCTGAGC) Antisense strand (SEQ ID No. 2: ACTCCTGCTTGCTGATCCAC)

[0102] M1 Viral Nonstructural Protein NS1 Primer:

TABLE-US-00003 Sense strand (SEQ ID No. 3: GTTCCAACAGGCGTCACCATC) Antisense strand (SEQ ID No. 4: ACACATTCTTGTCTAGCACAGTCC)

[0103] Methods:

[0104] 5×10.sup.6Hep3B cells were dorsa subcutaneously injected into 4-week-old nude mice. After four days, each mouse was injected with M1 virus via tail vein (3×10.sup.7 PFU). After administration, the nude mice were killed respectively at 1, 2, 3 and 4 days, and the tissue samples were collected (including tumor, heart, liver, spleen, lung, kidney, brain, and muscle), and RNAs is tissues were extracted. Then, the quantity of the M1 virus was determined by QRT-PCR method, in order to determine the M1 virus non-structural protein NS1 representing the M1 virus quantity. In the meanwhile the β-actin internal reference was determined, and relative quantity of the M1 virus RNA was calculated according to formula: 2.sup.−(C.sub.t-NS1.sup.−C.sub.t-internal reference.sup.). The .sup.C.sub.t-NS1 and .sup.C.sub.t-internal reference were from instrument reading in Applied Biosystems 7500 Fast Real-Time PCR System.

[0105] Results:

[0106] As shown in FIG. 2d, in the nude mouse subcutaneous Hep3B tumor model, at four different time points, the M1 virus quantity in the tumor tissues is 10.sup.2-10.sup.6 times more than that in other organ tissues, indicating a selective enrichment of the M1 virus in the tumor tissues.

Example 3. M1 Virus Selectively Caused Cell Death in ZAP Low Expression/ZAP Negative Tumors

[0107] M1 virus selectively caused cell death of the tumors with ZAP low expression, but had no effect on normal cells. It was indicated that the expression level of ZAP was the decisive factor of M1 virus selectivity. In normal cells and tumor cells with ZAP normal expression/high expression, by interfering RNA and knockdown of expression level of ZAP, the M1 virus could significantly cause cell death. Meanwhile, in the low ZAP expression tumor cell, by an overexpression of ZAP, the tumor cell death caused by the M1 virus was partially blocked.

1) M1 Virus Did not Cause Cell Death of the Normal Cells and Tumors with ZAP High Expression.

[0108] Materials:

[0109] M1 virus, human liver cell L-02, human glial cell HEB, human bladder cancer cell SCaBER and T24, human liver cancer cell line Hep3B and PLC, human liver cancer cell line Hep G2, human colorectal cancer cell line LoVo and HCT116; Western bolt: cell total protein extract (M-PER® Mammalian Protein Extraction Reagent, Thermo), ZAP antibody (Thermo, USA), β-actin antibody (Neomarker, USA);

Extracting RNA. PCR: RNA extraction reagent Trizol, a real-time quantitative PCR instrument, Applied Biosystems 7500 Fast Real-Time PCR System (Life, USA),

[0110] ZAP Primer:

TABLE-US-00004 ZAP sense strand (SEQ ID No. 5: TCACGAACTCTCTGGACTGAA) ZAP antisense strand (SEQ ID No. 6: ACTTTTGCATATCTCGGGCATAA)

[0111] β-actin primer is the same as Example 2.

[0112] Methods:

[0113] The cells in exponential growth phase were selected, and added into a DMEM or F-12 complete medium (containing 10% of fetal bovine serum and 1% of double antibody) to prepare a cell suspension, the cells were inoculated into a 35 mm well at a density of 2×10.sup.5/well. RNA was extracted, and ZAP mRNA expression quantity in the cells was determined by PCR. The internal reference of this experiment was β-actin. ZAP mRNA normalized expression quantity was calculated according to the formula: ZAP normalized mRNA expression quantity=2.sup.−(C.sub.t-ZAP.sup.−C.sub.t-internal reference.sup.). The .sup.C.sub.t-ZAP and .sup.C.sub.t-internal reference were from instrument reading of Applied Biosystems 7500 Fast Real-Time PCR System, and they represented for the cycle number corresponding to the threshold when the fluorescence signal began to enter the exponential growth stage from the background during PCR amplification.

[0114] The cell total protein was extracted, quantified, and a Western Blot experiment was conducted (electrophoresis, transmembrane, blocking, incubation of primary antibody and secondary antibody, and development). The ZAP and internal reference β-actin band grey scale were scanned by an imaging software Image Lab, the band grey scale was detected, and the ZAP normalized protein expression quantity was calculated according to the following formula: ZAP normalized protein expression quantity=ZAP band grey scale/internal reference band grey scale. The experiments were repeated for 3 times, and an average value was taken, to calculate the ZAP normalized protein expression quantity.

[0115] Results:

[0116] As shown in FIGS. 3a and 3b, in tumor cell SCaBER, T24, Hep3B and LoVo, mRNA (FIG. 3a) and protein (FIG. 3b) normalized expression quantity of the ZAP were almost undetectable, which was significantly lower than that in the normal cells (L-02 and HEB) and the tumor cells (PLC, HCT116).

[0117] The M1 virus caused cell death of ZAP low expression/negative tumor, but did not cause cell death of ZAP high expression tumor. There was no change of statistical significance in survival rate after the normal cells (L-02 and HEB) and a part of the tumor cells (PLC, HCT116) were infected by the M1 virus. The survival rate of L-02 was 100.3%, and HEB was 98.8% (Table 1). After infection with the M1 virus, the cell survival rate of tumor cell SCaBER, T24, Hep3B and LoVo were significantly reduced to T24 21.1%, SCaBER 11.5%, LoVo 6.9% and Hep3B 3.8% (Table 1).

[0118] As shown in FIG. 3c and Table 1, the ZAP protein normalized expression quantity of Hep G2 liver cancer cells is lower than that of L-02 normal cells, and the ratio of the two was 0.8. After the L-02 cell was infected by the M1 virus, survival rate was not obviously altered, while for the Hep G2 cell, after it was infected by the M1 virus, the survival rate was reduced to 70.4%. There was a statistical difference between these two types of cell. This further indicated that M1 virus selectively caused cell death of ZAP low expression tumor.

[0119] 2) M1 Virus Significantly Caused Cell Death of Normal Cells and Tumors after a Knockdown of ZAP Level.

[0120] Materials:

[0121] M1 virus, human liver cell L-02, human liver cancer cell PLC, human colorectal cancer cell HCT116, ZAP RNA interference fragment, MTT (methyl thiazolyl tetrazolium), Lipofectamine™ RNAiMAX (invertrogen, USA) Western bolt: cell total protein extract (M-PER® Mammalian Protein Extraction Reagent, Thermo), ZAP antibody (Thermo, USA), M1 virus NS3 antibody (Beijing Protein Innovation), M1 virus E1 antibody (Beijing Protein Innovation), GAPDH antibody (CST, USA); Extracting RNA, PCR: Trizol, a real-time quantitative PCR instrument (Applied Biosystems 7500 Fast Real-Time PCR System), β-actin, and M1 virus non-structural protein NS1 primer being the same as Example 2:

TABLE-US-00005 ZAP interference fragment (Si RNA) designed for target sequence SEQ ID No. 7: 5′ CCAAGAGTAGCACTTGTTA3′ Si RNA sense strand (SEQ ID No. 8: 5′CCAAGAGUAGCACUUGUUA dTdT 3′) Si RNA antisense strand (SEQ ID No. 9: 3′ dTdT GGUUCUCAUCGUGAACAAU 5′)

[0122] ZAP messy code interference fragment control (siNC): the nucleotide ratio of sense strand and antisense strand is the same as that of Si RNA fragment, but order of arrangement is completely random.

[0123] Methods:

[0124] The cells in the exponential growth phase were selected, and added into a DMEM complete medium (10% fetal bovine serum, 1% double antibody) to prepare a cell suspension, and the cells were inoculated into a 6-well plate at a density of 1×10.sup.5/well. After 24 hours, Si RNA fragment wrapped with RNAiMAX was added. After 48 hours, cells were infected with the M1 virus. After 48 hours of the infection, the specimens were treated.

[0125] MTT 20 μl (5 mg/ml) was added into each well, and after four hours, the absorbance value was determined, and cell survival rate was calculated. The siZAP experiment group was treated with the ZAP RNA interference fragment, and the siNC control group was treated by ZAP messy code interference fragment.

[0126] a) The cell supernatant was collected, and the virus titer was detected by TCID50 method.

[0127] b) RNA specimens were extracted, performed with PCR, and the M1 virus quantity was determined by detecting a quantity of M1 virus non-structural protein NS1. β-actin was the internal reference.

[0128] c) The protein specimen was extracted, ZAP protein expression and M1 virus protein NS3 and E1 were detected by Western blot, and the internal reference was GAPDH. The calculation of the ZAP normalized expression quantity was the same as 1) of Example 3 except that β-actin is replaced by GAPDH as the internal reference).

[0129] d) The experiment was repeated for 3 times, the data was represented by mean value±standard deviation; student's test statistics was conducted by comparing with respective control groups, */#/ & represented P<0.05, **/ & & represented P<0.01, ns represented no statistical difference.

[0130] Results:

[0131] As shown in FIG. 3d-3g, after human normal liver cell L-02, human liver cancer cell PLC and human colorectal cancer cell HCT116 were treated with ZAP RNA interference fragment, ZAP protein expression quantity was significantly reduced to an undetectable level (FIG. 3g), while M1 virus protein NS3 and E1 protein were obviously increased; after an infection with M1 virus (MOI=100), the survival rate of the L-02 cell (siZAP group) with a knockdown of ZAP level was significantly reduced to 69.7%±3.45%, the survival rate of PLC cell with a knockdown of ZAP level was reduced to 63.9%±11.5%, and the survival rate of HCT116 cell with a knockdown of ZAP level was reduced to 49.6%±1.21% (FIG. 3d); as shown in FIG. 3e, after 48 hours of infection with the M1 virus, the relative M1 virus titer in the L-02 cell with a knockdown of ZAP (siZAP group) was of 4.10±1.38 times of that in the corresponding siNC group; while for HCT116 cell (siZAP group), it was of 3.39±1.27 times of that in the corresponding siNC group; while for PLC cell (siZAP group), it was of 32.6±2.34 times of that in the corresponding siNC group. Meanwhile, as shown in FIG. 3f, after 48 hours of infection with the M1 virus, the M1 virus RNA expression quantity in the L-02 cell with a knockdown of ZAP (siZAP group) was of 16.3±8.20 times of that in the corresponding siNC group; while for HCT116 cell, it was of 8.82±4.02 times of that in the corresponding siNC group; while for PLC cell, it was of 30.5±12.23 times of that in the corresponding siNC group. The above results indicated that M1 virus significantly caused normal cell and tumor cell death after a knockdown of the ZAP level.

[0132] 3) tumor cell death induced by M1 virus was antagonized by an overexpression of ZAP.

[0133] Materials: M1 virus, human liver cancer cell Hep3B, pReceiver-M02-GFP plasmid for expressing GFP (blank control plasmid, Guangzhou Funeng Gene Co., Ltd.), pReceiver-M02-ZAP plasmid for expressing ZAP (overexpressed ZAP plasmid), FuGENE HD transfection reagent, MTT (methyl thiazolyl tetrazolium)

[0134] Extracting RNA, PCR: Trizol, a real time quantitative PCR instrument (Applied Biosystems 7500 Fast Real-Time PCR System), β-actin, M1 virus non-structural protein NS1 primer being the same as Example 2.

[0135] Western bolt: cell total protein extract (M-PER® Mammalian Protein Extraction Reagent, Thermo), ZAP antibody (Thermo, USA), M1 virus NS3 antibody (Beijing Protein Innovation), M1 virus E1 antibody (Beijing Protein Innovation), GAPDH antibody (CST, USA).

[0136] Methods:

[0137] The cells in exponential growth phase were selected, and added into DMEM complete medium (10% of fetal bovine serum and 1% of double antibody) to prepare a cell suspension, then the cells were inoculated in a 6-well plate at a density of 1×10.sup.5/well. After 24 hours, the cells were the transfected with overexpressed GFP control plasmids and ZAP overexpression plasmids, respectively, to obtain the corresponding cells expressing green fluorescent protein and the cells of ZAP overexpression. After 48 hours, the infection treatment with M1 virus was performed. After 48 hour of infection, the specimen was treated and detected.

[0138] a) The cell survival rate was determined by MTT method. MTT 20 μl (5 mg/ml) was added into each well, and after four hours, the absorbance value was detected at wavelength of 570 nM. Other treatments conducted were the same as Example 1.

[0139] b) The cell supernatant was collected, and the virus titer was detected by TCID50 method.

[0140] c) Total RNA specimen of the sample was extracted, and the RNA expression quantity of M1 virus was determined by QRT-PCR method, and calculated according to the method of Example 2.

[0141] d) The protein specimens were collected, ZAP protein expression quantity and M1 virus protein NS3, E1 protein expression quantity were detected by Western blot, and the treatment method was the same as 1 of Example 3).

[0142] e) Each experiment was repeated for three times, and the data were represented by mean value±standard deviation. Student's test was adopted for statistics by comparing with corresponding control groups. # represented for P<0.05, ** represented for P<0.01, and ns represented for the difference has no statistical significance.

[0143] Results:

[0144] As shown in FIG. 3k, after the human liver cancer cell Hep3B was transfected with the ZAP overexpression plasmid, the grey scale of the ZAP and the internal reference β-actin band in different specimens were scanned by Image Lab software, and respective ZAP normalized protein expression quantities were calculated. The ZAP normalized protein expression quantity in the ZAP overexpression group was 1.61±0.05, while in the overexpressed GFP control group it was 0.03±0.01. The mean value of the former was of 53.7 times of that of the latter; M1 virus protein NS3 and E1 protein were obviously increased;

[0145] As shown in FIG. 3h, an overexpression of ZAP partially blocked Hep3B cell death caused by M1 virus infection. After 48 hours of the infection by using different M1 virus titers, when MOI=0.1, the mean value of cell survival rate in the overexpressed ZAP group was 74.7%±8.94%, which was significantly higher than the cell survival rate in the overexpressed GFP control group (59.0%±6.27%); when MOI=1, the mean value of the cell survival rate in the overexpressed ZAP group was 69.4%±6.95%, which was significantly higher than the cell survival rate in the overexpressed GFP control group (51.4%±5.31%); when MOI=10, the mean value of cell survival rate in the overexpressed ZAP group was 63.7%±6.04%, which was significantly higher than the cell survival rate in the overexpressed GFP control group (40.5%±3.19%);

[0146] As shown in FIG. 3i, after the infection treatment with the M1 virus, the relative virus titer in the Hep3B cell with overexpressed ZAP was of 31.5±11.6% of that in the corresponding overexpressed GFP control group. Meanwhile, after M1 virus infection treatment, the M1 virus RNA expression quantity in the Hep3B cell with overexpressed ZAP was of 9.5±4.7% of that in the corresponding overexpressed GFP control group.

Example 4. M1 Virus Inhibited the Growth of ZAP Low Expression Human Ex Vivo Living Tumor Tissue (Ex Vivo)

[0147] Materials:

[0148] DMEM high glucose medium, TECIA (Tissue Culture-MTT Endpoint Computer Image Analysis Chemo-sensitivity Test), β-actin and ZAP primer is same as 1) of Example 3.

[0149] Methods:

[0150] a) Culture of Human Ex Vivo Living Liver Cancer Tissue and Colorectal Cancer Tissue

[0151] The ex vivo living tissue was obtained by surgical excision in Tumor Prevention Center of Sun Yat-sen University, stored at 4□, and then sent to the laboratory within four hours for drug sensitivity test. All the cases were confirmed by a histopathology examination. Under sterile condition, the tumor tissue was taken out, and cut into tissue pieces with a diameter of 0.5-1 mm, placed onto a 24-well culture plate (4-6 pieces per well), and 1 ml DMEM medium was added into each well. After one hour of culture, a projection illuminated image of the tumor tissue piece was taken by an image analyzer specialized for drug sensitivity test. The area of the tumor piece was determined and compared (area, A), to analyze the inhibitory effect of the M1 virus against the human ex vivo living tumor tissue.

[0152] b) Drug Treatment and Tissue Activity Determination

[0153] The tumor tissue was cultured in a CO.sub.2 cell incubator for 12 hours. After the status was stable, 10.sup.7 PFU of M1 virus and the positive control drug 5-fluorouracil (5-Fu, 10 mg/L) were added. After 96 hours of the infection treatment, MTT (5 mg/ml) was added at 50 μl/well, and cultured for 3 hours. A diffusion light illuminated image of the tumor tissue piece was then taken by an image analyzer specialized for drug sensitivity test, to determine the blue dyed area by formazan in the tumor piece in each well and the coloring degree (blue area, BA). Then the tissue survival rate (survival fraction, SF) was calculated according the following formula:

[00001]$\mathrm{SF}=\frac{{\mathrm{BA}}_{\mathrm{drug}.Math..Math.\mathrm{treatment}}/A_{\mathrm{drug}.Math..Math.\mathrm{treatment}}}{{\mathrm{BA}}_{\mathrm{control}}/A_{\mathrm{control}}}\times 100.Math.\%$

Tumor tissue inhibition rate (Cell inhibition, CI): CI, (1−SF)×100%, BA.sub.drug treated represented for blue dyed area of M1 virus/5-Fu treated group, A.sub.drug treated represented for area of tumor piece of M1 virus/5-Fu treated group, BA.sub.control represented for blue dyed area of the solvent control treated group, and A.sub.control represented for the area of tumor piece in the solvent control treated group.

[0154] c) Determination of ZAP mRNA Normalized Expression Quantity

[0155] According to a standard of tumor inhibition rate of 10%, all the above-mentioned case tissues were divided into two groups. The RNA of the specimens were respectively extracted, and levels of the ZAP mRNA and β-actin (internal reference) were determined by QRT-PCR method. The difference in ZAP normalized expression quantities between the two groups was compared. Rank-sum test was adopted for statistical analysis. The method for calculating the ZAP normalized expression quantity is the same as 1) of Example 3.

[0156] Results:

[0157] a) As shown in Table 2, for the liver cancer tissue, the ratio of cases with the inhibition rate more than 10% was 59.5% in the M1 virus group, which was higher than that in the 5-Fu group (53.8%). It was proved that the effectiveness rate of the M1 virus treatment was higher than the current 5-Fu drug treatment for clinical therapy for liver cancer.

TABLE-US-00006 TABLE 2 M1 virus and 5-Fu inhibiting the survival rate of human ex vivo living liver cancer tissues Inhibition rate M1 virus treatment 5-Fu treatment (% control) (%) (%)  >10% 22(59.5%) 14(53.8%) ≦10% 15(40.5%) 12(46.2%) Number of cases 37 26

[0158] b) As shown in Table 3, for the colorectal cancer tissues, the ratio of cases in which the inhibition rate being more than 10% was 71.4% in the M1 virus group, which was higher than that in the 5-Fu group (61.5%). It was proved that the effectiveness rate of M1 virus treatment was higher than the current 5-Fu drug treatment for clinical therapy for colorectal cancer.

TABLE-US-00007 TABLE 3 M1 virus and 5-Fu inhibiting the growth of human ex vivo living colorectal cancer tissue Inhibition rate M1 virus treatment 5-Fu treatment (% control) (%) (%)  >10% 10(71.4%) 8(61.5%) ≦10%  4(28.6%) 5(38.5%) Number of cases 14 13

[0159] c) The above-mentioned human ex vivo living tumor tissues which were treated by the M1 virus were divided into two groups according to an inhibition rate of 10%. The correlation of the ZAP mRNA expression level with the inhibition rate in these tissues was further analyzed. The ZAP normalized expression quantity of the group with a M1 virus treatment inhibition rate of more than 10% was 0.117±0.890, which was lower than that in the group with an inhibition rate of less than or equal to 10% (0.791±0.108). The ratio of the mean value of the two groups was 0.148. As shown in FIG. 4, the median of tumor tissue ZAP normalized expression quantity in the group with a M1 virus treatment inhibition rate of less than or equal to 10% was 0.414, and the median of tumor tissue ZAP expression quantity in the group with a M1 virus treatment inhibition rate of more than 10% was 0.075. Rank-sum test method was adopted for statistics. The difference had a statistical significance (P<0.05), indicating that the M1 virus could selectively cause tissue death in ZAP low expression/ZAP negative tumors.

Example 5. Low Expression of ZAP in Various Types of Tumor Clinical Pathological Tissues

[0160] Materials:

[0161] Eight tissue chips from 506 patients (including liver cancer, colorectal cancer, bladder cancer and paired paracancerous tissue), ZAP antibody (Thermo, USA), and APERIO fully automatic digital pathology slice scanner.

[0162] Methods:

[0163] The eight tissue chips from multiple centers was subjected to Immunohistochemical staining (IHC), scanned by APERIO scanner, and the staining density was calculated with a matching software, to determine the ZAP normalized expression quantity. ZAP normalized expression quantity=ZAP staining intensity within visual field/cell numbers within visual field. The cell number within visual field was used as homogenization standard.

[0164] Results:

[0165] Using an immunohistochemical method, the inventors determined the ZAP expression in various types of human tumor pathological specimens. FIG. 5a showed representative mappings for immunohistochemical staining of ZAP in human liver cancer, colorectal cancer, and bladder cancer pathological tissue specimens. Staining results of ZAP in the tumor tissues were lighter than those in the corresponding paracancerous tissues.

[0166] As shown in FIG. 5b, statistical analysis for the mean value of the ZAP protein homogenize expression quantity in liver cancer, colorectal cancer, bladder cancer and corresponding paracancerous non-neoplastic tissues was conducted. The results indicated that the averaged ZAP protein normalized expression quantity in the above-mentioned each type of tumor tissues was significantly lower than that in the corresponding paracancerous non-neoplastic tissues, indicating a low expression of ZAP in the tumor tissues. The averaged ZAP normalized expression quantity in all liver cancer tumor tissues was 5.83±8.49, which was significantly lower than that in the corresponding paracancerous non-neoplastic tissues (11.8±11.5). The ratio of these two average values was 0.494. The averaged ZAP normalized expression quantity in all colorectal cancer tumor tissues was 2.41±3.60, which was significantly lower than that in the corresponding paracancerous non-neoplastic tissues (8.30±8.94). The ratio of these two average values was 0.290. The averaged ZAP normalized expression quantity of all the bladder cancer tumor tissues was 2.93±4.63, which was lower than that in the paracancerous non-neoplastic tissues (10.3±8.36). The ratio of these two average values was 0.284.

[0167] As indicated in FIG. 5c, within all the liver cancer cases analyzed, the case number of ZAP low expression was of a percentage of 69%. Within all the colorectal cancer cases analyzed, there was a percentage of 52% of cases with ZAP low expression. Within all the bladder cancer cases analyzed, there was a percentage of 61% of cases with ZAP low expression. ZAP becomes a selective molecular marker for M1 viral antitumor therapy for liver cancer, colorectal cancer and bladder cancer.

Example 6. Preparation Method of the M1 Virus

[0168] Materials:

[0169] African Green Monkey kidney cell Vero, high glucose DMEM medium, OptiPRO™ SFM medium (lx), M1 virus, 100 mm cell culture dish, centrifuger.

[0170] Methods:

[0171] The cells in the exponential growth phase were selected, and added into a DMEM complete medium (containing 10% fetal bovine serum and 1% double antibody) to prepare a cell suspension. Then the cells were inoculated into a 100 mm cell culture dish. When a cell fusion degree reached 80%-90%, the medium was replaced with OptiPRO™ SFM medium. Then, 50 μl (MOI=0.01) M1 virus was added for infection treatment. When a large area of pathological changes occurred in the cell (about 36 hours), the cell supernatant was collected. The cell supernatant was centrifuged at 2000-3000 RPM for 5 minutes, then the supernatant was carefully sucked out, mixed and subpackaged, and stored at a −80□ refrigerator.

[0172] The above-described examples are illustration of the exemplary embodiment and effect of the present disclosure. However, the embodiment of the present disclosure is not limited to the above-described examples. Any other change, modification, substitution, combination, and simplification without departing from the spirit and principle of the present disclosure are all included in the protection scope of the present disclosure.