Scalarane sesterterpenoid, pharmaceutical composition and topoisomerase II and Hsp90 inhibitor for treating cancer, and use and preparation method thereof

Abstract

The present invention discloses scalarane sesterterpenoids represented by formula (I) and meroditerpenoid represented by formula (II), which are extracted from Carteriospongia sp. sponge: ##STR00001##
where R.sub.1 is CH.sub.3 or C.sub.2H.sub.5. The compounds of formula (I) can be used to be an anticancer, act as an inhibitor targeting to topoisomerase II and hsp90 and a pharmaceutical composition for anticancer.

Claims

1. A treatment method for treating a lymphoma of a subject, the method comprising: administering a pharmaceutically effective amount of a topoisomerase II inhibitor of formula (I) to the subject in need thereof: ##STR00004## where R.sub.1 is one of CH.sub.3 and C.sub.2H.sub.5.

2. The treatment method according to claim 1, wherein the topoisomerase II inhibitor of formula (I) is prepared by steps of: (a) providing a sponge animal; (b) extracting the sponge animal with ethyl acetate to obtain an ethyl acetate extract; (c) concentrating the ethyl acetate extract to obtain a residue; and (d) chromatographing the residue to obtain the topoisomerase II inhibitor of formula (I).

3. The treatment method according to claim 2, wherein the step (d) further comprises: (d1) sequentially chromatographing the residue with n-hexane, a plurality of n-hexane-ethyl acetate mixtures of an increasing polarity, and acetone on a silica gel to obtain a plurality of fractions; and (d2) purifying at least one of the plurality of fractions with a normal phase high performance liquid chromatography to obtain the topoisomerase II inhibitor of formula (I).

4. The treatment method according to claim 2, wherein the sponge animal is Carteriospongia sp.

5. The treatment method according to claim 2, wherein the topoisomerase II inhibitor of formula (I) with R.sub.1 being CH.sub.3 acts as a heat shock protein 90 (hsp90) inhibitor.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The objectives and advantages of the present invention will become more readily apparent to those ordinarily skilled in the art after reviewing the following detailed descriptions and accompanying drawings.

(2) FIG. 1 is a diagram showing the .sup.1H-.sup.1H COSY (-) HMBC (.fwdarw.) and NOESY (.Math.) correlations of compound 1 of the present invention.

(3) FIG. 2(A) is an electrophoretic gel diagram showing the effect of compounds 1 to 3 on the Topo II activity. Lanes 1-5: compound 3 (0.08, 0.3125, 1.25, 5, and 20 g/mL); Lanes 6-10: compound 1 (0.08, 0.3125, 1.25, 5, and 20 g/mL); Lanes 11-15: compound 2 (0.08, 0.3125, 1.25, 5, and 20 g/mL); Lane 16: positive control, etoposide (500 M), as a topo II poison (induction of linear DNA); Lane 17: plasmid DNA+topo II+solvent control (induction of DNA relaxation); Lane 18: Linear DNA; Lane 19: negative control plasmid DNA (supercoiled DNA).

(4) FIG. 2(B) shows the expression of H2AX protein in Molt 4 cells induced by the treatment of the marine terpenoids (compounds 1 to 3) of the present invention. The cells were treated with compounds 1 to 3 (0, 0.0625, 0.125 and 0.25 g/mL) for 24 hours, respectively. Protein expression was analyzed with Western blotting. GAPDH was used as the loading control.

(5) FIG. 3(A) is a diagram showing the effect of compound 3 on the tumor growth in an in vivo human Molt 4 tumor xenograft animal model. Tumor-bearing nude mice were intraperitoneally injected with solvent control (DMSO) and compound 3 (1.14 g/g) for 33 days. Tumor volumes were measured every other day, and the results are expressed as meanSD. *Significantly different from control groups at *p<0.05; **p<0.01. Control, n=8; compound 3, n=7.

(6) FIG. 3(B) is a diagram showing the effect of compound 3 on the body weight in the in vivo human Molt 4 tumor xenograft animal model. Tumor-bearing nude mice were intraperitoneally injected with solvent control (DMSO) and compound 3 (1.14 g/g) for 33 days. The body weight were measured every other day, and the results are expressed as meanSD. Control, n=8; compound 3, n=7.

(7) FIG. 4(A) is a diagram showing the effect of compound 1 on the ROS generation in Molt 4 cells.

(8) FIG. 4(B) is a diagram showing the effect of compound 1 on the ER-related protein in Molt 4 cells.

(9) FIG. 4(C) is a diagram showing the effect of compound 1 on the calcium accumulation in Molt 4 cells.

(10) FIG. 4(D) is a diagram showing the effect of compound 1 on the apoptosis-related proteins in Molt 4 cells.

(11) FIG. 4(E) is a diagram showing the effect of compound 1 on the comet-tail in Molt 4 cells.

(12) FIG. 5(A) is a diagram showing the cytotoxic effect of 17-AAG on Molt 4 cells.

(13) FIG. 5(B) is a diagram showing the effect of compound 1 on the expression of Hsp90 client proteins.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(14) The present invention will now be described more specifically with reference to the following embodiments. It is to be noted that the following descriptions of preferred embodiments of this invention are presented herein for purpose of illustration and description only; they are not intended to be exhaustive or to be limited to the precise form disclosed.

(15) Extraction and Isolation:

(16) The specimen of Carteriospongia sp. was collected by scuba diving at a depth of 14 m from coral reefs off the coast of Tai-tung, Taiwan in March, 2013. Voucher specimen was deposited in the National Museum of Marine Biology and Aquarium, Taiwan (specimen No. 2013-03-SP-3). Taxonomic identification was performed by the National Sun Yat-sen University, Kaohsiung, Taiwan. Because Carteriospongia sp. can be easily obtained and identified by the skilled person in the art, there is no need to reserve this biological material according to the Patent Law and its Implementing Regulations.

(17) Carteriospongia sp. (440 g fresh weight) was collected and freeze-dried. The freeze-dried material was minced and extracted exhaustively with ethyl acetate (EtOAc, 62 L). The EtOAc extract was evaporated under reduced pressure to afford a residue (5 g), and the residue was subjected to column chromatography on silica gel, using n-hexane, n-hexane and EtOAc mixture of increasing polarity, and finally pure acetone to yield 8 fractions: Fr-1 (eluted by n-hexane:EtOAc, 50:1 (v/v)), Fr-2 (eluted by n-hexane:EtOAc, 25:1 (v/v)), Fr-3 (eluted by n-hexane:EtOAc, 10:1 (v/v)), Fr-4 (eluted by n-hexane:EtOAc, 5:1 (v/v)), Fr-5 (eluted by n-hexane:EtOAc, 2:1 (v/v)), Fr-6 (eluted by n-hexane:EtOAc, 1:1 (v/v)), Fr-7 (eluted by EtOAc) and Fr-8 (eluted by acetone). Fraction 2 (560.0 mg) was separated by normal phase HPLC with gradient elution (n-hexane:EtOAc=50:1 (v/v) to 25:1 (v/v)) to yield 15 subfractions (2A-2O). Subfraction 21 was separated by normal phase HPLC (n-hexane:EtOAc=40:1 (v/v)) to afford compound 3 (70.0 mg). Fraction 5 (320.0 mg) was further purified with silica gel (n-hexane:EtOAc=4:1 (v/v) to 1:1 (v/v)) to afford 10 subfractions (5A-5J). Subfraction 5E was then separated by normal phase HPLC (n-hexane:EtOAc=3:1 (v/v)) to obtain compound 2 (6.0 mg). Subfraction 5G was separated by normal phase HPLC (n-hexane:EtOAc=3:1 (v/v)) to afford compound 1 (4.1 mg).

(18) Compound 1:

(19) 12-(3-hydroxybutanoyloxy)-20,24-dimethyl-24-oxo-scalara-16-en-25-al: colorless oil; [].sub.D.sup.25+10.7 (c 0.41, CHCl.sub.3); IR (neat) v.sub.max 3448, 2963, 2931, 2875, 1718, 1666, 1374 and 1272 cm.sup.1; .sup.13C and .sup.1H NMR data, see Table 1; ESIMS m/z 523[M+Na].sup.+; HRESIMS m/z 523.3397 [M+Na].sup.+ (calcd for C.sub.31H48O.sub.5Na, 523.3399).

(20) Compound 2:

(21) 12-(3-hydroxypentanoyloxy)-20,24-dimethyl-24-oxo-scalara-16-en-25-al (2): colorless oil; [].sub.D.sup.25+5.7 (c 0.50, CHCl.sub.3); IR (neat) v.sub.max 3448, 2930, 2854, 1730, 1666, 1388 and 1281 cm.sup.1; .sup.13C and .sup.1H NMR data, see Table 1; ESIMS m/z 537[M+Na].sup.+; HRESIMS m/z 537.3546 [M+Na] (calcd for C.sub.32H.sub.50O.sub.5Na, 537.3550).

(22) Preparation of (R)- and (S)-MTPA Esters (2r and 2s):

(23) A small amount of compound 2 (2.5 mg) was divided, stored in two nuclear magnetic resonance (NMR) tubes and dried under vacuum. Deuterated pyridine (0.60 mL) and (R)-MTPA-Cl (12 L) were added to one of the NMR tubes. The reaction NMR tubes were permitted to stand at room temperature and monitored by 400 MHz NMR every hour. After 3 hours, the reaction was found to be completed, and the .sup.1H NMR data was obtained (400 MHz, in C.sub.5D.sub.5N). The (S)-MTPA ester of compound 2 (compound 2s) was obtained, and the .sup.1H NMR data was analyzed. Similar to compound 2s, (S)-MTPA-Cl (12 L) and deuterated pyridine (0.60 mL) were reacted at room temperature for 3 hours, to afford the (R)-MTPA ester derivative (compound 2r), in separate experiment, and the .sup.1H NMR spectrum was measured with 400 MHz NMR in C.sub.5D.sub.5N. (S)-MTPA ester (compound 2s): .sup.1H NMR (400 MHz, C.sub.5D.sub.5N): 9.928 (d, J=3.6 Hz, 1H, H-25), 7.015 (s, 1H, H-16), 5.810 (t, J=6.4 Hz, 1H, H-3), 5.027 (dd, J=10.8, 4.8 Hz, 1H, H-12), 3.253 (s, 1H, H-18), 2.255 (s, 3H, H-26), 1.134 (s, 3H, H-23), 1.110 (t, J=6.0 Hz, 3H, H-5), 0.882 (s, 3H, H-21), 0.793 (s, 3H, H-22), 0.776 (s, 3H, H-19), 0.743 (t, J=7.2 Hz, 3H, H-25). (R)-MTPA ester (compound 2r): .sup.1H NMR (400 MHz, C.sub.5D.sub.5N): 10.018 (d, J=4.0 Hz, 1H, H-25), 7.065 (s, 1H, H-16), 5.833 (t, J=6.4 Hz, 1H, H-3), 5.123 (dd, J=11.2, 4.0 Hz, 1H, H-12), 3.393 (s, 1H, H-18), 2.259 (s, 3H, H-26), 1.142 (s, 3H, H-23), 1.060 (t, J=6.4 Hz, 3H, H-5), 0.885 (s, 3H, H-21), 0.797 (s, 3H, H-22), 0.780 (s, 3H, H-19), 0.745 (t, J=7.2 Hz, 3H, H-25).

(24) Bioassay Materials:

(25) The cell lines were obtained from the American Type Culture Collection (ATCC, Manassas, Va., U.S.A.) or the Japanese Collection of Research Biosources (JCRB) Cell Bank (Japan). Cells were maintained in RPMI 1640 medium supplemented with 10% fetal calf serum, 2 mM glutamine and antibiotics (100 units/mL of penicillin and 100 g/mL of streptomycin) at 37 C. in a humidified atmosphere of 5% CO.sub.2. Antibodies against c-PARP, caspases 8, 9, 7 and 3, H2AX, Bip, Grp 94, p-GSK 313 (Ser.sup.9), p-c-Raf, p70.sup.S6K, Hsp 90, Hsp 70, Rb 2, MDM2, HIF 1, PERK and IRE 1 were purchased from Cell Signaling Technologies (Beverly, Mass., U.S.A.). Antibodies against XIAP, NFB (p65), GADD, CDK 4, HSF 1, ATF 6 and -tubulin were obtained from Santa Cruz Biotechnology (Santa Cruz, Calif., U.S.A.). The Hybond ECL transfer membrane and ECL Western blotting detection kits were obtained from Amersham Life Sciences (Amersham, U.K.).

(26) Annexin V/Propidium Iodide (PI) Apoptosis Assay:

(27) The externalization of phosphatidylserine (PS) and membrane integrity were quantified using an annexin V-fluorescein isothiocyanate (annexin V-FITC) staining kit. In brief, 10.sup.6 cells were grown in 35 mm diameter plates and were labeled with annexin V-FITC (10 g/mL) and PI (20 g/mL) prior to harvesting. After labeling, all plates were washed with a binding buffer and harvested. Cells were resuspended in the binding buffer at a concentration of 210.sup.5 cells/mL before analysis by flow cytometer FACS-Calibur (Becton-Dickinson, San Jose, Calif., U.S.A.) and CellQuest software. Approximately 10,000 cells were counted for each determination.

(28) Determination of Reactive Oxygen Species (ROS) Generation, Calcium Accumulation, and Matrix Metalloproteinase (MMP) Disruption:

(29) MMP disruption, calcium accumulation and ROS generation were detected with the JC-1 cationic dye (5 g/mL), the fluorescent calcium indicator (Fluo 3, 5 mM) and the carboxy derivative of fluorescein (carboxy-H2DCFDA, 1.0 mM), respectively. In brief, the treated cells were labeled with a specific fluorescent dye for 30 minutes. After labeling, cells were washed with PBS and resuspended in PBS at a concentration of 110.sup.6 cells/mL before analysis via flow cytometry.

(30) Assay of Topoisomerase II Catalytic Inhibitors and Poisons:

(31) The assay was performed as described in the literatures (Shih et al., Marine Drugs, 2014, 12(5):3072-3090 and Shih et al., Marine drugs, 2015, 13(5):3132-3153). Standard relaxation reaction mixtures (20 L) containing 50 mM Tris-HCl (pH 8.0), 10 mM MgCl.sub.2, 200 mM potassium glutamate, 10 mM dithiothreitol, 50 g/mL bovine serum albumin (BSA), 1 mM ATP, 0.3 g of pHOT1 plasmid DNA, 2 units of human topoisomerase II (Topogen, Columbus, Ohio, U.S.A.), and the indicated concentrations of etoposide and the compounds 1 to 3 were incubated at 37 C. for 30 minutes. Reactions were terminated by adding 2 L of 10% SDS to facilitate trapping the enzyme in a cleavage complex, followed by the addition of 2.5 L of proteinase K (50 g/mL) to digest the bound protein (incubated at 37 C. for 15 minutes) and finally by adding 0.1 volume of the sample loading dye. The DNA products were analyzed via electrophoresis through vertical 2% agarose gels at 2 voltage/cm in 0.5TAE buffer. Gels were stained with ethidium bromide (EtBr) and photographed using an Eagle Eye II system (Stratagene, La Jolla, Calif., U.S.A.). The quantitative analysis of the DNA Topo II activity was performed. The gels were directly scanned with an image analyzer, and the area representing supercoiled DNA calculated to evaluate the concentration that the compounds caused 50% inhibition (IC.sub.50) of Topo II activity.

(32) Neutral Comet Assay for Detection of DNA Double-Strand Breaks (DSBs):

(33) The assay was carried out using a CometAssay Kit (Trevigen, Gaithersburg, Md., U.S.A.) following the manufacturer's protocol for the neutral Comet assay. Briefly, cancer cells (210.sup.5 cells/mL) were treated with compound 1 (0.0625 g/mL) at the indicated time. Cells were combined with 1% low melting point agarose at a ratio of 1:10 (v/v) and immediately 75 L of the mixture was pipetted onto CometSlide and allowed to set at 4 C. in the dark. The slides were immersed in an ice-cold lysis solution (Trevigen) for 30 to 60 minutes. The slides were placed in a horizontal electrophoresis apparatus and electrophoresed in 1TBE (90 mM Tris-HCl, 90 mM boric acid, and 2 mM EDTA, pH 8.0) at 20 V for 10 minutes. The samples were then fixed in 70% ethanol and dried before stained with 1:10,000 SYBR Green I (Trevigen) to visualize cellular DNA. The fluorescence images were analyzed using the TriTek Comet Image program to circumscribe the head and the tail regions of each comet and the integrated fluorescence values of each defined area were recorded. The comet length was measured from the trailing edge of the nucleus to the leading edge of the tail. This length was indicative of the extent of DNA damage. Calculations were averaged per replicate. The results were expressed as meanstandard deviation (SD) (*p<0.05).

(34) Immunofluorescence Analysis:

(35) After treatment with the tested compound, cells were fixed with 4% paraformaldehyde in 50 mM HEPES buffer (pH 7.3) for 30 minutes, and permeabilized for 20 minutes with 0.2% Trition X-100 in PBS (pH 7.4). To prevent non-specific protein binding, cells were incubated with 5% BSA in PBS containing 0.05% Trition X-100 (T-PBS) for 1 hour at room temperature. Cells were then incubated with the primary Hsp70 antibodies (1:500) for 2 hours and further with secondary antibodies (Alexa Fluor 586-conjugated goat anti-mouse IgG (H+L) (Life Technologies, Carlsbad, Calif., U.S.A.)) diluted at 1:1000 for 1 hour at room temperature. After washing with PBS, cells were observed under a FV1000 confocal laser scanning microscope (Olympus, Tokyo, Japan).

(36) Human Leukemia Molt 4 Cells Xenograft Animal Model:

(37) Six-week-old male immunodeficient athymic mice were purchased from the National Laboratory Animal and Research Center (Taipei, Taiwan). All of the animals were maintained under standard laboratory conditions (temperature 24-26 C., 12-12 hour dark-light circle) and fed with a laboratory diet and water. Molt 4 cells (110.sup.6) resuspended in 0.2 mL PBS were injected subcutaneously (s.c.) into the right flank of each mouse, and tumor growth was monitored every day. Fourteen (14) days after tumor cell injection, mice with confirmed tumor growth were randomly divided into two groups. Compound 3 (1.14 g/g) was intraperitoneally administered to the treatment group, and the control group received solvent only. Compound 3 was administrated every other day for 33 days. Animals were sacrificed by carbon dioxide. Tumor size was measured three times a week using calipers and tumor volumes were calculated according to the standard formula: width.sup.2length/2.

(38) Molecular Modeling Assay:

(39) The molecular docking was performed by Autodock 4.2 with Lamarckian Genetic Algorithm (Morris et al., J. Comput. Chem., 2009, 30(16):2785-2791.). The target macromolecule, Hsp90 protein (PDB ID: 1YET), was obtained from the Protein data bank (http://www.rcsb.org/pdb/home/home.do). The co-crystalized protein substrates, including ligands, water and small molecules were removed, and the Polar hydrogens and Kallman united atom charges were added to the protein for docking calculation by AutoDock Tool 1.5.4 interfaces (ADT). The ligands were optimized with MMFF94 force field by ChemBio3D software (version 11.0; Cambridge Soft Corp.). Polar hydrogens and Gasteiger charges were also added to the ligand for docking study by ADT. The Grid box calculated by AutoGrid program was centered at the activity site of Hsp90 with dimensions 565656 grid points at spacing of 0.375 and its size is big enough to allow the ligand move freely in the search space. All docking parameters were set to default except for the following parameter: maximum number of energy evaluation increase to 25,000,000 per run. The docking results were analyzed by ADT and shown by Accelrys Discovery Studio v3.5 client software (Accelrys Inc, San Diego, Calif., U.S.A. (2005)).

(40) Statistics:

(41) The results were expressed as meanstandard deviation (SD). Comparison in each experiment was performed using an unpaired Student's t-test and a p value of less than 0.05 was considered to be statistically significant.

(42) Experimental Results:

(43) Chemical Identification of the Marine Terpenoids (Compounds 1 to 3):

(44) The EtOAc extract of the freeze-dried specimen was fractionated by silica gel column chromatography and the eluted fractions were further separated utilizing normal phase HPLC to yield compounds 1 to 3. The novel compound 1 was named as 12,-(3,-hydroxybutanoyloxy)-20,24-dimethyl-24-oxo-scalara-16-en-25-al, and the novel compound 2 was named as 12-(313-hydroxy-pentanoyloxy)-20,24-dimethyl-24-oxo-scalara-16-en-25-al. The known compound 3 was identified as 2-tetraprenil-1,4-benzochinone.

(45) Compound 1 was a colorless oil. The molecular formula of compound 1 was determined to be C.sub.31H48O.sub.6 by HR-ESI-MS (m/z 523.3397 [M+Na].sup.+) and .sup.13C NMR data (Table 1), implying eight degrees of unsaturation. IR absorptions were observed at 3448, 1717 and 1665 cm.sup.1, suggesting the presence of hydroxyl, saturated carbonyl and ,-unsaturated carbonyl functionalities. Resonances due to an aldehyde carbonyl carbon (.sub.C 201.1), ,-unsaturated carbonyl carbon (.sub.C 198.2), ester carbonyl carbon (.sub.C 172.1) and olefinic carbons (.sub.C 142.9, CH; 138.4, C) in the .sup.13C NMR and distortionless enhancement by polarization transfer (DEPT) spectral data accounted for four double-bond equivalents, indicating a tetracyclic skeleton of compound 1. In the .sup.1H NMR data, resonances of one olefinic proton (.sub.H 7.06, s) and two oxygenated methines (.sub.H 4.86, dd, J=11.0, 4.5 Hz; 4.22, t, J=9.0 Hz) were observed. The planar structure and all of the .sup.1H and .sup.13C chemical shifts of compound 1 were elucidated by 2D NMR spectroscopic analysis, in particular .sup.1H-.sup.1H correlation spectroscopy (COSY) and heteronuclear multiple bond correlation (HMBC) experiments (referring to FIG. 1), suggesting a characteristic scalarane-type sesterterpenoid structure. Compound 1 possess a 3-hydroxybutanoyloxy at C-12, a double bond at C-16/C-17, a ketone group at C-24 and an aldehyde group at C-25. The 3R-configuration was determined by comparing the optical rotation (+10.7) of compound 1 with those of compound 2 (+5.7). Therefore, the structure of compound 1 possess the (4S*, 5S*, 8R*, 9R*, 10S*, 12R*, 13S*, 14S*, 18R*, 3R*)-configuration.

(46) TABLE-US-00001 TABLE 1 .sup.1H and .sup.13C NMR data of compounds 1 and 2 (.sup.1H: 500 MHz in CDCl.sub.3; .sup.13C: 125 MHz in CDCl.sub.3.) Compound 1 Compound 2 Position .sub.C .sub.H (J in Hz) .sub.C .sub.H (J in Hz) 1 40.1, CH.sub.2 0.88, 1.64 m 40.1 0.87, 1.64 m 2 18.1, CH.sub.2 0.84 m 18.1 0.84, 1.44 m 3 36.5, CH.sub.2 0.87 m; 1.66 br s 36.5 0.87, 1.66 m 4 36.1, C 36.1 5 58.4, CH 0.87 m 58.4 0.88 m 6 17.9, CH.sub.2 0.85 m 17.9 0.87 m 7 41.9, CH.sub.2 1.75 m 42.0 1.74 m 8 37.5, C 37.5 9 58.0, CH 0.99 m 58.0 1.01 br s 10 37.4, C 37.4 11 23.3, CH.sub.2 1.40 q (12.5); 23.2 1.88 m 1.87 dd (12.5, 4.0) 12 82.5, CH 4.86 dd (11.0, 4.5) 82.5 4.87 dd (11.0, 4.5) 13 41.7, C 41.7 14 53.0, CH 1.21 m 53.0 1.22 m 15 23.6, CH.sub.2 2.34 br t 23.6 2.34 m 16 142.9, CH 7.06 s 142.8 7.06 s 17 138.4, C 138.5 18 61.2, CH 3.15 s 61.2 3.17 s 19 28.4, CH.sub.3 0.80 s 28.4 0.79 s 20 24.4, CH.sub.2 1.15 q (7.5); 1.52 m 24.4 1.15, 1.50 m 21 16.9, CH.sub.3 0.96 s 16.9 0.96 s 22 17.3, CH.sub.3 0.85 s 17.3 0.85 s 23 10.9, CH.sub.3 0.98 s 10.9 0.98 s 24 198.2, C 198.2 25 201.1, CH 9.64 d (3.5) 201.2 9.65 d (3.0) 26 25.0, CH.sub.3 2.28 s 25.0 2.28 s 27 8.6, CH.sub.3 0.74 t (7.5) 8.6 0.74 t (7.5) .sup.1 172.1, C 172.3 .sup.2 43.4, CH.sub.2 2.42 m 41.6 1.14, 1.36 m .sup.3 64.3, CH 4.22 t (9.0) 69.4 3.96 t (11.0) .sup.4 22.5, CH.sub.3 1.24 d (6.5) 29.5 2.32 m .sup.5 9.9 0.96 t (4.0)

(47) The molecular formula of compound 2 was deduced as C.sub.32H.sub.50O.sub.5 based on HR-ESI-MS (ion peak at m/z 537.3546 [M+.sub.Na]).sub.+ and .sup.13C NMR data suggesting that compound 2 possesses one more CM group compared with compound 1. The NMR data of compound 2 (Table 1) showed similarity to those of compound 1 with the replacement of one 3-hydroxybutanoyloxy group at C-12 in compound 1 by one 3-hydropentanolyoxy group in compound 2. The structure of compound 2 was further confirmed by the COSY correlations from H.sub.2-29 to H.sub.3-32 and by the HMBC correlations from H-12 and H.sub.2-29 to C-28. Both compounds 1 and 2 were suggested to possess identical relative configuration based on the similarity in their NMR data. In order to identify the C-3 configuration on the 3-hydroxybutanoyloxy group, the (S)- and (R)-MTPA ester derivatives, 2s and 2r, were synthesized with ()-(R)-MTPA-Cl and (+)-(S)-MTPA-Cl, respectively. The -values indicated 3R-configuration (data not shown).

(48) Apoptotic Induction of these Marine Terpenoids Via DNA Damage, MMP Dysfunction and Caspase Activation:

(49) The antiproliferative effect of the two novel scalarane sesterterpenoids (compounds 1 and 2) and the compound 3 (as a tetraprenyltoluquinol-related metabolite) was evaluated using the MTT assay known by the skilled person in the art. Several cancer cell lines including leukemia K562, Molt 4, and HL 60 cells, prostate cancer LNCaP cells, colon cancer DLD-1 cells and breast cancer T-47D cells were used to evaluate the antiproliferative activity (referring to Table 2). Compound 1 exhibited the most potent cytotoxic activity with an IC.sub.50 of 0.01 g/mL (2.08 nM) against all leukemia and the lymphoma cell line U937. After a 72-hour treatment, the IC.sub.50 values of compound 1 against DLD-1, T-47D, LNCaP, Ca9-22 and Cal-27 cells were 2.33, 2.19, 13.87, 0.1, and 0.56 g/mL, respectively. The IC.sub.50 values of compound 2 against leukemia K562, Molt 4 and HL 60 cells were 0.35 and 0.30, 0.22 g/mL which were comparable to those of compound 3 (IC.sub.50 values: 0.70, 0.34 and 0.42 g/mL). Molt 4 cell line was the most sensitive cell line as demonstrated by the MTT assay known by the skilled person in the art. To detect whether the cytotoxic effect of these marine terpenoids was associated with the mitochondria-related apoptosis, the population of apoptosis and disruption of mitochondrial membrane potential in Molt 4 cells with annexin-V/PI and JC-1 staining were assessed. After 24 hours, compounds 1, 2 and 3 resulted in a dose-dependent (0, 0.0625, 0.125 and 0.25 g/mL) increase in the apoptotic population of Molt 4 cells and disruption in mitochondrial membrane potential (data not shown). These results proved that the cytotoxic activity of these marine terpenoids are mediated through the mitochondrial dysfunction leading to the induction of apoptosis.

(50) TABLE-US-00002 TABLE 2 Cytotoxic effects of compounds 1 to 3 against several cancer cell lines for 72 hours (IC.sub.50, g/mL) Leukemia Lymphoma Oral Prostate Colon Breast Compound K562 Molt 4 HL 60 U937 Sup-T1 Ca9-22 Cal-27 LNCaP DLD-1 T-47D 1 0.01 0.01 0.01 0.01 0.13 0.10 0.56 13.87 2.33 2.19 2 0.35 0.30 0.22 0.61 0.42 1.48 3.17 NA.sup.a 1.71 1.87 3 0.70 0.34 0.42 0.65 0.33 0.97 0.51 NA.sup.a 15.41 1.06 Doxorubicin.sup.b 0.20 0.01 0.02 0.21 0.02 0.05 0.01 2.47 1.28 0.08 .sup.aNA (non-active) = IC.sub.50 >20 g/mL for 72 hours. .sup.bPositive control

(51) In order to confirm whether the DNA damage-induced by the marine terpenoids of the present invention involved the inhibition of Topo II activity, a cell-free DNA cleavage assay using an enzyme-mediated negatively supercoiled pHOT1 plasmid DNA was applied. A linear DNA strand was observed upon treating the supercoiled pHOT1 plasmid DNA with etoposide, a standard topo II poison (FIG. 2(A), Lane 16, the control group). The use of compound 1 in increasing concentrations (0.08, 0.312, 1.25, 5, and 20 g/mL) significantly inhibited DNA relaxation by 12, 13, 17, 20 and 99%, respectively, compared with the control supercoiled DNA and resulted in the formation of supercoiled DNA products in the presence of topo IIa (FIG. 2(A), Lanes 6-10). Additionally, compounds 2 and 3 significantly inhibited DNA relaxation by 12, 23, 36, 90 and 99% (FIG. 2(A), Lanes 11-15); and 7, 13, 28, 90 and 98% (FIG. 2(A), Lanes 1-5), respectively. These marine terpenoids suppressed Topo II activity, resulting in the inhibition of supercoiled DNA relaxation in a dose-dependent manner (FIG. 2(A)). Furthermore, compounds 1, 2 and 3 inhibited topo II activities with IC.sub.50 of 1.98, 0.37 and 0.43 g/mL, respectively as demonstrated by the cell-free system. To determine whether the apoptotic mechanism of compounds 1 to 3 affects H2AX (as a biomarker of DNA damage) induction, Western blot analysis was employed to examine the activation of H2AX. Compounds 1 and 2 significantly enhanced the expression of H2AX in a dose-dependent manner, but the activation of DNA damage was not observed on compound 3 (FIG. 2(B)). These results suggested that these compounds 1 to 3 could act as potent catalytic inhibitors of Topo IIa.

(52) Compound 3 Inhibited Tumor Growth in In Vivo Human Molt 4 Tumor Xenograft Animal Model:

(53) Compounds 1 and 2 induced apoptosis in several cancer cell lines. On the other hand, compound 3 was used to study the in vivo anti-tumor activity by evaluating its effect on tumor growth of human leukemia Molt 4 in xenograft animal model. Molt 4 (110.sup.6) cells were inoculated subcutaneously at the right flank of female immunodeficient athymic mice. After 33-day of treatment, the tumor growth of Molt 4 cells was significantly suppressed under the influence of compound 3 (1.14 g/g) intraperitoneal injection. The average tumor size on day 33 in the control group was 404.63 mm.sup.3, whereas the average tumor size in compound 3-treated group was 212.10 mm.sup.3 (FIG. 3(A)). The tumor size was significantly lower in compound 3-treated group as compared to the control group (p<0.05) with no significant difference in the mice body weights (FIG. 3(B)). These results suggested that compound 3 exhibited anti-tumorigenic effect in vivo xenograft model.

(54) Apoptotic Effect of Compound 1 Involves the Induction of ROS Generation, Endoplasmic Reticulum (ER) Stress and DNA Damage in Molt 4 Cells:

(55) Oxidative stress is manifested by ROS overexpression and cannot be balanced by the available antioxidant machinery. Compound 1 of the present invention can damage the integrity of mitochondria, which are the major production sites of the superoxide anion, ozone. The induction of the intracellular formation of ROS by compound 1 was determined with a carboxyl derivative of fluorescein, carboxy-H2DCFDA dye using flow cytometric analysis. As shown in FIG. 4(A), treatment with compound 1 (0.0625 g/mL) for 0.5, 1, 2 and 3 hours resulted in 2.09-, 1.51-, 1.06- and 1.01-fold increase in ROS levels, respectively, as compared with the mean fluorescence index (MFI) of the control. In addition, ROS generation could induce ER stress leading to mitochondria-related apoptosis. To further investigate if ER stress is involved in the apoptotic effect induced by compound 1, Western blot analysis was used to determine the expression of ER stress-related proteins. In a time-dependent manner, compound 1 promoted the levels of Bip, Chop, Grp 94 and the activation and cleavage of ATF 6 but suppressed the levels of PERK and IRE 1. Furthermore, the effect of compound 1 on the release of intracellular Ca.sup.2+, was evaluated using fluorescent calcium indicator, Fluo 3. As shown in FIG. 4(C), the flow cytometric results showed that the treatment with compound 1 at different time intervals (0.5, 1, 2, 3, 6 and 18 hours) induced 1.03-, 1.05-, 1.06-, 1.37-, 2.41- and 1.06-folds increase in the intracellular Ca.sup.2+ accumulation, respectively as compared to MFI of the control, indicating that ER stress was induced by compound 1 following the redox stress. Moreover, as shown in FIG. 4(D), PARP, caspases-8 and -9 cleavages were significantly increased in a time-dependent manner. In FIG. 4(D), the induction of the typical executor caspases-3 and -7, and H2AX, was also observed using Western blot analysis. To confirm the induction of DNA damage by compound 1 in Molt 4 cells, a comet assay under neutral electrophoresis condition was utilized. Thus, the effect of compound 1 (0.0625 g/mL) at different time intervals (0, 3, 6 and 9 hours) on the level of nuclear DNA integrity was determined. As shown in FIG. 4(E), compound 1 increased the degree of DNA migration in Molt 4 cells. The DNA migration was represented by the induction of DSBs in a time-dependent increase, as indicated by the abnormal tails' sizes in the comet assay.

(56) Compound 1 as a Potent Inhibitor of Hsp90:

(57) It is known that mitochondria are critical intracellular loci of ROS production and ROS exposure can lead to the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (mPTP) opening. The antioxidant, microsomal GST1, in the inner mitochondrial membrane can interact with the mitochondrial permeability transition (MPT) regulator proteins, such as ANT and/or CypD, to form a MPT pore contributing to mitochondria-mediated cell death. In addition, mitochondrial homeostasis of tumor cells is regulated by an organelle-specific Hsp90 chaperone network. To investigate whether the inhibition of Hsp90 participates in the apoptosis induced by compound 1, the molecular docking of Hsp90 with the available crystal structure was performed to gain insight of the compound 1 binding mode. Compound 1 could be docked to the N-terminal domain of Hsp90 with the binding energy of 10.93 Kcal/mol over the first Hsp90 N-terminal inhibitor, 17-AAG (6.63 Kcal/mol), presumably because compound 1 formed non-classic hydrogen bonds with GLY132 and GLY135 at a distance of 3.27 and 3.66 ; the classic hydrogen bonds with residues LYS112 (1.92 ), PHE138 (2.31 and 2.45 ) and ASN106 (2.45 ); the hydrophobic bonds with residues ALA 55 (3.63 and 3.69 ) and MET 98 (3.85 and 4.96 ) (data not shown). According to the molecular docking experiments, compound 1 inhibits Hsp90 with an inhibition constant of 9.67 nM (>1430 folds) which was more potent than 17-AAG (10.83 M). To fully understand the differences in activity between compound 1 and 17-AAG, the antiproliferative activity of 17-AAG in Molt 4 cells was examined by the MTT assay. As shown in FIG. 5(A), treatment of Molt 4 with increasing concentrations (0, 0.4, 2 and 10 M of 17-AAG for 24 hours induced a suppression in cell growth with IC.sub.50 values of 4.2 g/mL (7.2 M). According to the MTT results using Molt 4 cells, the antiproliferative activity of compound 1 (0.01 g/mL, 19.1 nM) was 377 folds higher than that of 17-AAG.

(58) Hsp90 inhibitors induced the heat shock factor 1 (HSF 1)-dependent expression of Hsp70, and the genetic deletion of HSF 1 reduced the association of Hsp90 with its kinase client proteins. The induction of Hsp70 is the biomarker of Hsp90 with N-terminal inhibition. Aiming to understand the relation between Hsp90 function and the expression of Hsp70 and 90 clients, Molt 4 cells were treated with compound 1 (0.0625 g/mL) for different time intervals. At first, the compound 1 treatment did not notably attenuate the expression of Hsp90 protein. The expression of Hsp70 increased in a time-dependent manner, as an established marker for the heat shock response (HSR) after Hsp90 inhibition, while surprisingly the expression of HSF 1 protein was attenuated with the compound 1 treatment in Molt 4 cells. Furthermore, as shown in FIG. 5(B), Hsp90 client proteins were suppressed, including p70.sup.S6K, NFB, Raf-1, p-GSK3, MEK 1 and XIAP (pro-apoptotic protein), MDM 2 and Rb2 (oncoprotein), and CDK4 (cell cycle regulatory protein), HIF 1 and HSF1 (transcription factor). The majority of Hsps accumulate in subcellular localizations that determine whether a cell is going to die or differentiate. Furthermore, the localization of Hsp70 in response to the compound 1 treatment was identified using immunofluorescence by confocal microscope. In agreement with the Western blot results, the localization of Hsp70 was predominantly accumulated in cytosol and the accumulation increased with time (data not shown).

(59) The Advantages of the Present Invention:

(60) Two scalarane sesterterpenoids (compounds 1 and 2) and a known tetraprenyltoluquinol-related metabolite (compound 3) are isolated from the EtOAc extract of the sponge animal, Carteriospongia sp., in the present invention. All compounds 1 to 3 can be used in the anticancer, the reduction of the viability of cancer cells, and the inhibition of the Topo II catalytic activity. Compound 1 results in the abundant release of Ca.sup.2+ and interferes the mitochondrial membrane potential, indicating that its apoptotic effect is mediated through the mitochondrial dysfunction. As demonstrated by the increase in the ROS generation, ATF6 cleavage and Chop expression, the compound 1-treatment firstly stimulates the ROS generation, perturbs the Bip/IRE1/PERK signal pathway and activates the Grp94/ATF6/Chop signal pathway implicated in ER stress, and the cytotoxic effect of compound 1 on the human leukemia Molt 4 cells is relevant to the induction of ER stress. Compound 1 possesses the potent Hsp90 and Topo II catalytic inhibitory activity as determined by the molecular docking and the cell-free system. The treatment of Molt 4 cells with compound 1 suppresses client protein expression and accumulation of Hsp70 in the cytosolic compartment as well as reduces the transcription factors (HSF 1 and HIF 1) expression.

(61) Therefore, compounds 1 to 3 of the present invention can be used in anticancer, act as the topoisomerase II inhibitor, and can be prepared as anti-tumor pharmaceutical composition according to the pharmaceutical techniques and method.

(62) While the invention has been described in terms of what is presently considered to be the most practical and preferred Embodiments, it is to be understood that the invention need not be limited to the disclosed Embodiments. On the contrary, it is intended to cover various modifications and similar arrangements included within the spirit and scope of the appended claims, which are to be accorded with the broadest interpretation so as to encompass all such modifications and similar structures.