Method of treating lung cancer using <i>Parabacteroides goldsteinii </i>

Abstract

The present disclosure provides a use of Parabacteroides goldsteinii for treating lung cancer.

Claims

1. A method of treating a lung cancer, comprising administering to a subject in need thereof a composition comprising an effective amount of a Parabacteroides goldsteinii; wherein the Parabacteroides goldsteinii is Parabacteroides goldsteinii DSM32939.

2. The method according to claim 1, wherein the composition further comprises a metabolite of the Parabacteroides goldsteinii.

3. The method according to claim 1, wherein the Parabacteroides goldsteinii is a live bacterium.

4. The method according to claim 1, wherein the effective amount of the Parabacteroides goldsteinii is at least 1×10.sup.9 CFUs per day.

5. The method according to claim 1, wherein the lung cancer is a non-small cell lung cancer.

6. The method according to claim 5, wherein the non-small cell lung cancer is a Lewis lung carcinoma.

7. The method according to claim 1, wherein the composition increases a survival rate, a mean survival time and a body weight of the subject with the lung cancer, and inhibits a growth of a lung tumor.

8. The method according to claim 7, wherein inhibiting comprises inhibiting the growth of the lung tumor at different time points.

9. The method according to claim 1, wherein the composition further comprises other bacteria.

10. The method according to claim 1, wherein the composition is a pharmaceutical composition or a food product.

11. The method according to claim 10, wherein the composition further comprises a pharmaceutically acceptable excipient, carrier, adjuvant, or food additive.

12. The method according to claim 1, wherein the composition is in the form of a spray, a solution, a semi-solid state, a solid state, a gelatin capsule, a soft capsule, a tablet, an oral strip, a chewing gum or a freeze-dried powder preparation.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows that the effect of the Parabacteroides goldsteinii MTS01 on increasing the survival rate of lung cancer mice.

(2) FIG. 2 shows that the effect of the Parabacteroides goldsteinii MTS01 on increasing the mean survival time of lung cancer mice.

(3) FIG. 3 shows that the effect of the Parabacteroides goldsteinii MTS01 on increasing the body weight of lung cancer mice. *p<0.05; ***p<0.001; NS means no significant difference.

(4) FIG. 4 shows that the appearance of the effect of the Parabacteroides goldsteinii MTS01 on inhibiting the growth of the lung tumor.

(5) FIG. 5 shows that the H&F stained images of the effect of the Parabacteroides goldsteinii MTS01 on inhibiting the growth of the lung tumor.

(6) FIG. 6 shows that the effect of the Parabacteroides goldsteinii MTS01 on inhibiting the growth of the lung tumor. **p<0.01; ***p<0.001.

(7) FIG. 7 shows that the bioluminescence images in vivo effect of Parabacteroides goldsteinii MTS01 on inhibiting lung cancer after Lewis Lung Carcinoma cells (LLC) implanted on the 7th day.

(8) FIG. 8 shows that the bioluminescence images in vivo effect of Parabacteroides goldsteinii MTS01 on inhibiting lung cancer after Lewis Lung Carcinoma cells (LLC) implanted on the 14th day.

(9) FIG. 9 shows that the bioluminescence images in vivo effect of Parabacteroides goldsteinii MTS01 on inhibiting lung cancer after Lewis Lung Carcinoma cells (LLC) implanted on the 21st day.

(10) FIG. 10 shows that the in vivo effect of the Parabacteroides goldsteinii MTS01 on inhibiting lung cancer at different time points. ***p<0.001.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Definition

(11) The data provides in the present invention represent approximated, experimental values that vary within a range of ±20%, preferably ±10%, and most preferably ±5%.

(12) Statistical analysis is performed using GraphPad prism 5.01 software (GraphPad Software Inc., San Diego, Calif.). Data are expressed as mean±standard deviation (SD), and differences between groups are statistically analyzed by one-way ANOVA and statistical analysis is performed by Dunnett's multiple comparison test.

(13) According to the present invention, the Parabacteroides goldsteinii is a Gram-negative, particularly anaerobic non-spore forming and non-moving bacterium, and is also a probiotic bacterium.

(14) According to the present invention, the probiotic or probiotic bacteria is a microorganism, the cells thereof, the mixed strains, the extracts or the metabolites with a positive effect on the host itself, usually derived from the human body and beneficial to intestinal health. Probiotic or probiotic bacteria can also refer to certain microorganisms that are externally supplemented and are beneficial to the body. Wherein, the metabolite of the probiotic or probiotic bacteria is a substance which is secreted into the bacterial culture solution after being metabolized by the bacteria.

(15) According to the present invention, the operating procedures and parameter conditions for bacterial culture are within the professional literacy and routine techniques of those having ordinary skill in the art.

(16) The “effective amount” describes herein is the amount of the Parabacteroides goldsteinii requires for direct treatment of individuals with lung cancer. The effective amount varies depending on the species or individual being treated, but the effective amount can be determined experimentally by, for example, a dose escalation test.

(17) The “metabolite” describes herein is a substance which is secreted into the bacterial culture solution after being metabolized by the bacteria.

(18) The “the bacterial component thereof” describes herein is a derivative substance directly or indirectly related to the bacterium when it is cultured, including but not limited to the metabolic product of the bacterium, the structure of the bacterium, the bacteria-related activity and the inactive ingredient, etc.

(19) The “Parabacteroides goldsteinii” describes herein is intended to encompass those of the Parabacteroides goldsteinii, which is readily available to those having ordinary skill in the art, for example, the Parabacteroides goldsteinii purchased from domestic or foreign depository institutions, and a strain of Parabacteroides goldsteinii isolated and purified from a natural source using a microorganism separation method conventionally used in the art.

(20) The “treating” or “treatment” describes herein means alleviating, reducing, ameliorating, relieving, or controlling a disease or one or more clinical signs of a disorder, and lowering, stopping, or reversing the progress of the severity of a condition or a symptom being treated.

(21) According to the present invention, the pharmaceutical composition can be manufactured into a dosage form suitable for parenterally or orally administration using techniques well known to those having skill in the art, including, but not limited to, an injection, for example, sterile aqueous solutions or dispersions, a sterile powder, tablets, a tablet, a lozenge, a pill, a capsule, a dispersible powder or a granule, a solution, a suspension, a emulsion, a syrup, an elixir, a slurry and the like.

(22) According to the present invention, the pharmaceutical composition can be administered by a parenteral route selected from the group consisting of the intraperitoneal injection, the subcutaneous injection, the intramuscular injection, and the intravenous injection.

(23) According to the present invention, the pharmaceutical composition could further comprise a pharmaceutically acceptable carrier that is widely used in pharmaceutical manufacturing techniques. For example, the pharmaceutically acceptable carrier can comprise one or more agents selected from the group consisting of a solvent, an emulsifier, a suspending agent, a decomposer, a binding agent, an excipient, a stabilizing agent, a chelating agent, a diluent, a gelling agent, a preservative, a lubricant, an absorption delaying agent, a liposome, and the like. The selection and quantity of these reagents falls within the professional literacy and routine skills of those having ordinary skill in the art.

(24) According to the present invention, the pharmaceutically acceptable carrier comprises a solvent selected from the group consisting of water, normal saline, phosphate buffered saline (PBS), sugary solution, aqueous solution containing alcohol, and combinations thereof.

(25) According to the present invention, the pharmaceutical composition can be used as a food additive, added by the conventional method in the preparation of the raw material, or added during the production of the food, and matched with any edible material to be made into food products for human and non-human animals.

(26) According to the present invention, the types of the food products include, but are not limited to, beverages, fermented foods, bakery products, health foods, and dietary supplements.

(27) The use of the Parabacteroides goldsteinii of the present invention in the treatment of lung cancer can be, but is not limited to, oral administration to the subject in need thereof. The composition can be orally administered along with food; therefore, the preparation of the composition comprising the Parabacteroides goldsteinii of the present invention can further include a protein, a monosaccharide, a disaccharide, an oligosaccharide, an oligosaccharide, a polysaccharide, a carbohydrate, an amino acid, a lipid, a vitamin, or any combination well-known in the art.

(28) Otherwise, the preparation of the composition comprising the Parabacteroides goldsteinii of the present invention can further include a pharmaceutically acceptable excipient, carrier, adjuvant, or food additive. The composition is in the form of, but is not limited to a spray gas, a solution, a semi-solid state, a solid, a gelatin capsule, a soft capsule, a tablet, a lozenge, a chewing gum, and/or a freeze-dried powder preparation. Simultaneously, the Parabacteroides goldsteinii of the present invention or the composition containing other ingredients can further use in the preparation of a food, a health food, a dietary supplement, or a vaccine composition.

Example 1

(29) Effect of Parabacteroides goldsteinii MTS01 on Increasing the Survival Rate of Lung Cancer Mice

(30) In the embodiment of the present invention, six-to-eight-week-old, specific pathogen-free, C57BL/6J male mice were purchased from National Applied Research Laboratories, NARLab, Taiwan. All mice were fed ad libitum with chow and water. Animals were housed in a temperature-controlled room (19-23° C.) under a 12 hours dark-light cycle. Animals were housed in a specific pathogen-free facility and were treated in accordance with guidelines from the National Institutes of Health (USA). In the following experiments, C57BL/6J male mice were injected with Lewis Lung Carcinoma (LLC) cells (1×10.sup.6 cells) in the tail vein, and then the growth and volume of the tumor were monitored throughout the experiment.

(31) The Parabacteroides goldsteinii (hereinafter referred to as P. goldsteinii) MTS01 used in the example of the present invention is a kind of probiotic bacteria, which can or treat lung cancer, and is deposited in Deutsche Sammlung von Mikroorganismen and Zellkulturen (DSMZ; Inhoffenstr. 7B, D-38124 Braunschweig, Germany) on Oct. 29, 2018, and the number is DSM 32939. The Parabacteroides goldsteinii is an obligate anaerobe that needs to be cultured in an anaerobic incubator at 37° C. for about 48 hours, wherein the culturing system contains 10% CO.sub.2, 10% H.sub.2, and 80% N.sub.2. The liquid culture medium of the Parabacteroides goldsteinii is NIH thioglycollate broth (TGC II) (purchased from BD, USA, No. 225710), and the solid culture medium is Anaerobic blood agar plate (Ana. BAP) (purchased from CREATIVE LIFESCIENCES, Taiwan). The Parabacteroides goldsteinii is stored in a −80° C. refrigerator for a long-term preservation, and the protective liquid is 25% glycerin. It does not need special cooling treatment and can be stored by freeze drying to stabilize its activity.

(32) The Parabacteroides distasonis (hereinafter referred to as P. distasonis) used in the example of the present invention was purchased from American Type Culture Collection, and the number is ATCC 8503. YCFA medium was used for culturing, wherein the Parabacteroides distasonis was cultured in 50 mL YCFA at 37° C. in an anaerobic incubator for 24 hr. The cell suspension for oral administration was prepared by suspending the cultured bacterial cells in oxygen-free PBS with a final cell density of 1×10.sup.9 CFU. 100 μL of the suspension solution was given daily.

(33) The non-small cell lung cancer, NSCLC, used in the example of the present invention is Lewis lung cancer (LLC) cells (purchased from ATCC, and the number is ATCC®CRL 1642™). The LLC cells were maintained in Dulbecco's modified Eagle's medium, DMEM, (purchased from Gibco, USA) supplemented with 10% fetal bovine serum (purchased from Gibco, USA), 100 U/mL of penicillin, and 100 μg/mL of streptomycin, and were incubated at 37° C. in a humidified atmosphere containing 5% CO.sub.2.

(34) Male C57BL/6J mice were randomly divided into the 4 groups (n=10 for each group), including the normal control group (CTL), the pathological control group (LLC), the experimental group (LLC+P. goldsteinii MTS01), and the comparison group (LLC+P. distasonis). The mice in the normal control group were treated with sterile drinking water and fed with PBS oral gavage once per day for 3 weeks; the mice in the pathological control group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and fed with PBS by oral gavage once per day during the entire period of experiment; the mice in the experimental group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides goldsteinii MTS01 (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment; the mice in the comparison group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides distasonis (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment. The results of this example were represented by three independent experiments (n=10) and the results were shown in FIG. 1.

(35) The results of the effect of the Parabacteroides goldsteinii MTS01 on increasing the survival rate of lung cancer mice were shown in FIG. 1. As showing in FIG. 1, after 21 days of intravenous injection of LLC cells, the survival rate of the mice in the pathological control group was 20%, and the survival rate of the mice in the experimental group was 50%, which was higher than that of the mice in the comparison group. The mice in the normal control were healthy and alive throughout the experiment. The results indicate that the Parabacteroides goldsteinii strain MTS01 of the present invention can increase the survival rate of mice with lung cancer.

Example 2

(36) Effect of Parabacteroides goldsteinii MTS01 on Increasing the Mean Survival Time of Lung Cancer Mice

(37) The experimental animals, the Parabacteroides goldsteinii, the Parabacteroides distasonis, and the type and the culturing method of the Lewis lung cancer were the same as those described in example 1.

(38) Male C57BL/6J mice were randomly divided into the 4 groups (n=10 for each group), including the normal control group (CTL), the pathological control group (LLC), the experimental group (LLC+P. goldsteinii MTS01), and the comparison group (LLC+P. distasonis). The mice in the normal control group were treated with sterile drinking water and fed with PBS oral gavage once per day for 4 weeks; the mice in the pathological control group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and fed with PBS by oral gavage once per day during the entire period of experiment; the mice in the experimental group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides goldsteinii MTS01 (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment; the mice in the comparison group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides distasonis (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment. The results of this example were represented by three independent experiments (n=10) and the results were shown in FIG. 2.

(39) The results of the effect of the Parabacteroides goldsteinii MTS01 on increasing the mean survival time of lung cancer mice were shown in FIG. 2. As showing in FIG. 2, the mean survival time of the mice in the experimental group was 22.6 days, which was higher than that of the mice in the pathological control group (19.3 days) (P<0.01) and that of the mice in the comparison group. The mice in the normal control were healthy and alive throughout the experiment. The results indicate that the Parabacteroides goldsteinii strain MTS01 of the present invention can increase the mean survival time of mice with lung cancer.

Example 3

(40) Effect of Parabacteroides goldsteinii MTS01 on Increasing the Body Weight of Lung Cancer Mice

(41) The experimental animals, the Parabacteroides goldsteinii, the Parabacteroides distasonis, and the type and the culturing method of the Lewis lung cancer were the same as those described in example 1.

(42) Male C57BL/6J mice were randomly divided into the 4 groups (n=10 for each group), including the normal control group (CTL), the pathological control group (LLC), the experimental group (LLC+P. goldsteinii MTS01), and the comparison group (LLC+P. distasonis). The mice in the normal control group were treated with sterile drinking water and fed with PBS oral gavage once per day for 4 weeks; the mice in the pathological control group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and fed with PBS by oral gavage once per day during the entire period of experiment; the mice in the experimental group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides goldsteinii MTS01 (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment; the mice in the comparison group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides distasonis (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment.

(43) In order to study the effect of the Parabacteroides distasonis MTS01 on improving the body weight loss in subjects caused by LLC, the body weight of each group of mice was monitored weekly for 4 weeks during the experiment. The final body weight at week 4 subtracted the starting weight at week 0 as the value of the body weight gain of each group of mice. The value of body weight gain was divided by the starting body weight and expressed as a percentage to calculate the body weight change rate of each group of mice. The results of the example were shown in FIG. 3.

(44) The results of the effect of the Parabacteroides goldsteinii MTS01 on increasing the body weight of lung cancer mice were shown in FIG. 3. As showing in FIG. 3, the body weight gain of the mice in the pathological control group was significantly lower than that of the mice in the normal control group. However, compared with the pathological control group, the body weight gain of the mice in the experimental group mice was significantly increased with the simultaneously fed with the Parabacteroides goldsteinii MTS01 of the present invention, whereas the mice in the comparison group did not show this phenomenon. The results indicate that the Parabacteroides goldsteinii strain MTS01 of the present invention can effectively improve the body weight loss in the subjects caused by LLC.

Example 4

(45) Effect of Parabacteroides goldsteinii MTS01 on Inhibiting the Growth of the Lung Tumor

(46) The experimental animals, the Parabacteroides goldsteinii, the Parabacteroides distasonis, and the type and the culturing method of the Lewis lung cancer were the same as those described in example 1.

(47) Male C57BL/6J mice were randomly divided into the 4 groups (n=10 for each group), including the normal control group (CTL), the pathological control group (LLC), the experimental group (LLC+P. goldsteinii MTS01), and the comparison group (LLC+P. distasonis). The mice in the normal control group were treated with sterile drinking water and fed with PBS oral gavage once per day for 3 weeks; the mice in the pathological control group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and fed with PBS by oral gavage once per day during the entire period of experiment; the mice in the experimental group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides goldsteinii MTS01 (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment; the mice in the comparison group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides distasonis (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment. The results of this example were represented by three independent experiments (n=10).

(48) After fed with the Parabacteroides distasonis MTS01 by oral gavage for 21 days, each group of mice was sacrificed, and the lungs were removed and the appearance of the lungs was observed. The results of the experiment were shown in FIG. 4.

(49) The appearance results of the effect of the Parabacteroides goldsteinii MTS01 on inhibiting the growth of the lung tumor were shown in FIG. 4. As showing in FIG. 4, the solid tumors (as indicated by the arrows) were spotted on multiple sites in the group bearing with LLC. Compared with the pathological control group, the number of lung tumors in the mice of the experimental group was significantly reduced, while the comparison group did not show the phenomena. The results indicate that the Parabacteroides goldsteinii strain MTS01 of the present invention can inhibit the growth of lung tumor.

(50) Next, the lung leaves of the mice in the normal control group (CTL), the pathological control group (LLC), and the experimental group (LLC+P. goldsteinii MTS01) were fixed in 10% neutral-buffered formalin, and then embedded in paraffin and thin sections with a thickness of 4 mm were prepared and stained with hematoxylin and eosin (H&E). Thereafter, the stained lungs were histologically examined using a slide scanner and the entire lung lobe was photographed (Olympus VS120). Representative images of whole slide scan and 500 μm or 250 μm optical zoom using H&E-stained lung sections. The results of the experiment were shown in FIG. 5.

(51) The H&E stained results of the effect of the Parabacteroides goldsteinii MTS01 on inhibiting the growth of the lung tumor were shown in FIG. 5. As showing in FIG. 5, compared with the normal control group, the number of lung tumors in the mice of the pathological control group was significantly increased. However, compared with the pathological control group, the number of lung tumors in the mice of the experimental group was significantly reduced. The results indicate that the Parabacteroides goldsteinii strain MTS01 of the present invention can inhibit the growth of lung tumor.

(52) Next, the lung tumors of the mice in the normal control group (CTL), the pathological control group (LLC), and the experimental group (LLC+Pg MTS01) were weighed, and the results of the experiment were shown in FIG. 6.

(53) The data results of the effect of the Parabacteroides goldsteinii MTS01 on inhibiting the growth of the lung tumor were shown in FIG. 6. As showing in FIG. 6, compared with the normal control group, the lung tumor weight of the mice in the pathological control group was significantly increased. However, compared with the pathological control group, the lung tumor weight of the mice in the experimental group was significantly reduced. The results indicate that the Parabacteroides goldsteinii MTS01 of the present invention can inhibit the growth of the tumor growth in the mouse model with lung tumors.

Example 5

(54) In Vivo Effect of Parabacteroides goldsteinii MTS01 on Inhibiting Lung Cancer at Different Time Points

(55) The experimental animals, the Parabacteroides goldsteinii, the Parabacteroides distasonis, and the type and the culturing method of the Lewis lung cancer were the same as those described in example 1.

(56) Male C57BL/6J mice were randomly divided into the 3 groups (n=10 for each group), including the normal control group (CTL), the pathological control group (LLC), and the experimental group (LLC+Pg MTS01). Wherein, the mice in the normal control group were treated with sterile drinking water and fed with PBS oral gavage once per day; the mice in the pathological control group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and fed with PBS by oral gavage once per day during the entire period of experiment; the mice in the experimental group were treated with Neomycin (1 g/L) in drinking water for 7 days, followed by LLC cells (1×10.sup.6) intravenous injection via tail vein and treated with Parabacteroides goldsteinii MTS01 (1×10.sup.9 CFU) once per day by oral gavage during the entire period of experiment. The results of this example were represented by three independent experiments (n=10).

(57) At the day 0, 7, 14, and 21 after implantation of LLC cells, the mice of each group were anesthetized with isoflurane and intraperitoneally injected with firefly D-luciferin (15 mg/mL in PBS; Gold Biotechnology), and then were imaged with a cooled charge-coupled device (CCD) camera (IVIS; PerkinElmer) after 7 minutes. In vivo imaging was performed with IVIS Lumina XR Imaging system (PerkinElmer). The luciferin dose was 150 mg/kg. The results of the example were shown in FIG. 7 to FIG. 10. The scale indicates luminescent intensity in terms of radiant efficiency.

(58) The bioluminescence imaging results of in vivo effect of Parabacteroides goldsteinii MTS01 on inhibiting lung cancer after LLC cells implanted on the 7th day were shown in FIG. 7. As showing in FIG. 7, compared with the normal control group, the luminescent intensity measured from the mice in the pathological control group was significantly increased. However, compared with the pathological control group, the luminescent intensity measured from the mice in the experimental group was significantly reduced. The results indicate that the Parabacteroides goldsteinii MTS01 of the present invention has an effect of inhibiting lung cancer after LLC cells implanted on the 7th day in vivo.

(59) The bioluminescence imaging results of in vivo effect of Parabacteroides goldsteinii MTS01 on inhibiting lung cancer after LLC cells implanted on the 14th day were shown in FIG. 8. As showing in FIG. 8, compared with the normal control group, the luminescent intensity measured from the mice in the pathological control group was significantly increased. However, compared with the pathological control group, the luminescent intensity measured from the mice in the experimental group was significantly reduced. The results indicate that the Parabacteroides goldsteinii MTS01 of the present invention has an effect of inhibiting lung cancer after LLC cells implanted on the 14th day in vivo.

(60) The bioluminescence imaging results of in vivo effect of Parabacteroides goldsteinii MTS01 on inhibiting lung cancer after LLC cells implanted on the 21st day were shown in FIG. 9. As showing in FIG. 9, compared with the normal control group, the luminescent intensity measured from the mice in the pathological control group was significantly increased. However, compared with the pathological control group, the luminescent intensity measured from the mice in the experimental group was significantly reduced. The results indicate that the Parabacteroides goldsteinii MTS01 of the present invention has an effect of inhibiting lung cancer after LLC cells implanted on the 21st day in vivo.

(61) The results of in vivo effect of the Parabacteroides goldsteinii MTS01 on inhibiting lung cancer at different time points were shown in FIG. 10. As showing in FIG. 10, compared with the normal control group, the luminescent intensity measured from the mice in the pathological control group increased significantly as the time of LLC cells implantation. However, compared with the pathological control group, though the luminescent intensity measured from the mice in the experimental group increased as the time of LLC cells implantation, but the increase range was significantly reduced. The results indicate that the Parabacteroides goldsteinii MTS01 of the present invention has an effect of inhibiting lung cancer at different time points in vivo.

(62) In summary, the effect of the Parabacteroides goldsteinii of the present invention is that the effect of treating lung cancer which is achieved by increasing the survival rate, the mean survival time, and the body weight of the subjects with lung cancer, and inhibiting the growth of the lung tumor.

(63) The above description is by way of example only and not as a limitation. Any equivalent modifications or alterations to the spirit and scope of the invention are intended to be included in the scope of the appended claims.