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Introduction

Synovial sarcoma (SS) is one of four common soft tissue sarcomas and accounts for 5–10% of the total incidence of soft tissue sarcomas. Diagnosis and classification of this malignant tumor type is difficult (1); ~40% of cases exhibit metastasis within 2 years (2) and the five-year survival rate of high-level SS is ~50–60% (3). Thus, there is a critical demand to establish effective therapeutic strategies for SS.

Doxorubicin is an anthracycline antibiotic widely used in clinical treatment of various types of cancer, including SS. It has been suggested that it functions primarily via insertion into DNA topoisomerase II, in order to cleave the DNA and destroy its structure (4). Doxorubicin is known to affect cells in all phases, but cells in the S phase are considered to be the most sensitive to doxorubicin (5). Doxorubicin is a recommended drug in the National Comprehensive Cancer Network Guidelines for Soft tissue Sarcoma (6), however it presents various side-effects, including nausea, vomiting, alopecia, high fever and bone marrow suppression. In particular, the cardiotoxic effects of doxorubicin limit its clinical application (7). Thus, the current study presents a novel combination therapy, which may be an improved treatment strategy.

Gossypol is an anticancer drug (8) that is able to significantly inhibit cancer cell proliferation and induce apoptosis in vitro (9–12). L-gossypol is the principal active component of gossypol, and certain cell types are 5-fold more sensitive to L-gossypol than gossypol (13). L-gossypol has various advantages over gossypol, including that it is more widely available, safer and has fewer reported side-effects (14). It has also been demonstrated to inhibit growth and promote apoptosis in squamous cell carcinoma (15). The aim of the present study was to investigate the effects of L-gossypol and low-concentration doxorubicin (LCD) combination therapy on growth inhibition and apoptotic induction in SW982 human SS cells (HSSCs). In the current study, the mechanisms of apoptosis induced by L-gossypol/LCD combination therapy were investigated in the SW982 cell line.

Materials and methods

Cell culture and experimental groups

SW982 cells were obtained from the American Type Culture Collection (Manassas, VA, USA) cultured in L-15 medium (Gibco Life Technologies, Grand Island, N Y, USA) containing 10% FBS (Gibco Life Technologies), 100 U/ml penicillin and 100 U/ml streptomycin (Shandong Lukang Record Pharmaceutical Co., Ltd., Jining, China), and were incubated at 37°C with 5% CO2. L-gossypol was provided by Professor Tang Hui, University of Shihezi (Shihezi, China). Doxorubicin (Bio Basic, Inc., Amherst, N Y, USA).

The experimental groups were divided as follows: i) Control group, cells cultured in the medium described; ii) L-gossypol group, 2.5 μmol/l L-gossypol; iii) doxorubicin group, 0.2 μmol/l doxorubicin; iv) combination group, 2.5 μmol/l L-gossypol and 0.2 μmol/l doxorubicin. The culture medium was replenished every 3–4 days and the cells were trypsinized (Gibco Life Technologies) and replated at 85% confluence.

MTT assay

MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide; MP Biomedicals, LLC, Santa Ana, CA, USA] assays were performed in accordance with the manufacturer's instructions. The effect of five different concentrations of doxorubicin (0.01, 0.02, 0.05, 0.1 and 0.2 μmol/l) and L-gossypol (0.0, 0.5, 1.0, 1.5, 2.0 and 2.5 μmol/l) were investigated. The drug combinations were designed in accordance with the factorial design and are listed in Table I.

Table I Drug and dose combinations by factorial design.

Table I

Drug and dose combinations by factorial design.

Combination	D0	D1	D2	D3	D4	D5
G0	G0D0	G0D1	G0D2	G0D3	G0D4	G0D5
G1	G1D0	G1D1	G1D2	G1D3	G1D4	G1D5
G2	G2D0	G2D1	G2D2	G2D3	G2D4	G2D5
G3	G3D0	G3D1	G3D2	G3D3	G3D4	G3D5
G4	G4D0	G4D1	G4D2	G4D3	G4D4	G4D5
G5	G4D0	G4D1	G4D2	G4D3	G4D4	G4D5

[i] D0-5 and G0-5 represent the concentrations (μmol/l) of doxorubicin and gossypol, respectively, used in the experiments. D0, 0; D1, 0.01; D2, 0.02; D3, 0.05; D4, 0.1; D5, 0.2; G0, 0; G1, 0.5; G2, 1.0; G3, 1.5; G4, 2.0; G5, 2.5.

The cells were seeded during the logarithmic growth phase onto 96-well plates at a density of 5×104 cells/ml (100 μl/well) with five parallel wells. The experimental drugs were added, resulting in a final volume of 200 μl/well. Subsequently, 20 μl MTT/well was incubated for 4 h at 37°C, then the supernatant was removed, 150 μl dimethyl sulfoxide was added, and the plates were incubated for a further 10 min. The absorbance was then measured using an xMark Microplate Absorbance Spectrophotometer (Bio-Rad Laboratories, Inc., Hercules, CA, USA) at a wavelength of 490 nm. The absorbance values at 24, 48, 72 and 96 h were measured in order to calculate the IC50 (the concentration resulting in 50% inhibition) and inhibitory rates using the following formula: Inhibitory rate = (1 - absorbance of the experimental group/absorbance of the control group) × 100%.

Cellular morphology

Wright-Giemsa staining (Nanjing Jiangcheng Bioengineering Institute, Nanjing, China) was conducted according to the manufacturer's instructions on 1×105 cells/ml seeded in 6-well plates, cultured for 24 h with the experimental drug. Cellular morphology was observed under an IX71 inverted optical microscope (Olympus Corporation, Tokyo, Japan). Hoechst 33258 (Sigma-Aldrich, St. Louis, MO, USA) staining was conducted on 1×106 cells per experimental group under the microscope. Ultrathin sections (70–90 nm) were cut from samples of the control and 24 h treatment groups using a Reichert Ultracut-E ultramicrotome (Reichert-Jung, Vienna, Austria). Cells from the prepared sections were visualized using transmission electron microscopy (TEM) on a JEOL 1230 Transmission Electron Microscope (JEOL, Ltd., Tokyo, Japan).

Flow cytometry

A total of 1×106 cells from each of the experimental and drug-treated (24 and 48 h) groups were collected and resuspended in 1 ml 10X annexin V binding buffer from a FITC Annexin V Apoptosis Detection Kit I (BD Biosciences, San Jose, CA, USA). A total of 100 l f of the solution was transferred into a cell culture tube; 5 μl fluorescein isothiocyanate (FITC)-annexin V and 5 μl propidium iodide (PI) from the kit were added. Simultaneously, FITC and PI were added to the blank well. Subsequent to mixing, the solution was cultured at room temperature in the dark for 15 min, 400 μl combined buffer was added into the cell culture tube, and flow cytometry was conducted using an Epics Altra Flow Cytometer (Beckman Coulter, Inc., Miami, FL, USA).

Detection of alterations in the cell cycle

A total of 1×106 cells from each of the experimental and drug-treated (24 and 48 h) groups were collected for flow cytometry. The cells were centrifuged at 300 × g for 5 min, washed twice with phosphate-buffered saline (PBS), fixed with 1 ml ice cold 70% ethanol and mixed, then maintained at 4°C for 24 h. Prior to testing, the mixture was centrifuged at 1,500 rpm for 5 min and washed twice with PBS prior to the addition of 400 μl RNA enzyme (30 μg/ml; Sigma-Aldrich). The cells were then incubated at 37°C for 30 min, mixed with 100 μl PI (200 μg/ml) and incubated in the dark at 4°C for 30 min prior to flow cytometry. The cell distribution percentages for the G1, S and G2 phases were then calculated using EXPO 32 MultiComp software, version 1.2 (Beckman Coulter, Inc.).

Western blotting

A total of 100 μg protein was collected from the experimental and 24 h drug-treated groups. Protein samples underwent polyacrylamide gel electrophoresis with 8% gel at 80 V (Wuhan Boster Biological Technology, Ltd., Wuhan, China) and were subsequently transferred onto polyvinylidene difluoride membranes. The samples were then blocked with nonfat milk and incubated overnight with polyclonal rabbit anti-human Bcl-2 (sc-782) or Bax (sc-493) primary antibodies (Santa Cruz Biotechnology, Inc., Dallas, TX, USA) overnight at 4°C. Blots were incubated with the horseradish peroxidase-conjugated secondary antibody (1:5,000; anti-IgG; Santa Cruz Biotechnology, Inc.). The secondary antibody was added and incubated at 37°C for 2 h and visualized using staining with 3,3′-diaminobenzidine (Beijing Solarbio Science & Technology Co., Ltd., Beijing, China). Quantity One 1-D analysis software, version 4.6.2 (Bio-Rad Laboratories, Inc.) was used for analysis of the grayscale values. The relative expression level of the target protein was calculated as follows: Target protein band gray value/internal reference (β-actin) gray value.

Caspase-3 and -9 activity analysis

A total of 1×106 cells were collected from each of the experimental and the drug-treated groups at 0, 6, 12, 18 and 24 h. These were analyzed using the Caspase-3 and Caspase-9 Colorimetric Assay kits (R&D Systems, Inc., Minneapolis, MN, USA), at a wavelength of 405 nm. The activity levels of caspase-3 and -9 in the control group were set as 1, while the optical density (OD) value/the control group OD was used to represent the activity of caspase-3 and -9 in the other groups. The formula used was as follows: Caspase-9 and -3 activity = (OD405 of sample - OD405 of blank)/(OD405 of control - OD405 of blank).

Statistical analysis

The current study used factorial design and the experiment was repeated three times with the results presented as the mean ± standard deviation. All data obtained were analyzed using SPSS software, version 18.0 (SPSS, Inc., Chicago, IL, USA). The data met the criteria for independence, normality and homogeneity of variance, therefore a t-test was selected for analysis. In addition, the χ2 test was used when appropriate, with the test level set as α=0.05. P<0.05 was considered to indicate a statistically significant difference.

Results

Cell proliferation

L-gossypol and LCD exhibited different degrees of time-dependent inhibition on the proliferation of SW982 cells (Fig. 1). The IC50s of L-gossypol were 16.2, 4.7, 3.9 and 2.5 μmol/l at 24, 48, 72 and 96 h, respectively, whereas those of LCD were 5.12, 1.06, 0.32 and 0.20 μmol/l at 24, 48, 72 and 96 h, respectively. In addition, the combined inhibitory effect of L-gossypol and LCD exhibited a clear increase in a concentration- and time-dependent manner (P<0.001), indicating a strong synergy between the two drugs (Fig. 1, Table II).

Figure 1 Impacts of different concentrations of doxorubicin and L-gossypol on the cell inhibition rate following 96 h-combination therapy.

Table II Analysis of variance.

Table II

Analysis of variance.

	Doxorubicin	L-gossypol	T	D,T	G,T	G,D	D,G,T
F-ratio	1175.682	750.205	4223.069	39.296	61.691	2.459	1.565
P-value	<0.001	<0.001	<0.001	<0.001	<0.001	<0.001	=0.005

[i] T, combined effect; D, doxorubicin; G, L-gossypol.

Inverted phase contrast microscopy

Wright-Giemsa staining was conducted on SW982 HSSCs cocultured in 2.5 μmol/l L-gossypol and/or 0.2 μmol/l doxorubicin for 48 h, which revealed distinct morphological differences between the groups (Fig. 2). Control cells were tightly packed, large and predominantly appeared as clostridial forms with few cells exhibiting the polygonal form. The nuclei were large and centrally located, and a small number of cells deviated from the standard form. The majority of cells in the control group were observed to have two nuclei and the cytoplasm was abundant. However, in the experimental groups, the number and size of the cells was significantly reduced. In addition, a larger number of cells appeared to be irregular in shape and a small number were circular. The nuclei were observed to shrink in certain cells, while in others the nuclei fragmented, the fragments of which were observed moving towards the outer part of cells, forming film-coated apoptotic bodies (Fig. 2).

Figure 2 Wright-Giemsa staining illustrating apoptosis of SW982 cells following the action of doxorubicin and L-gossypol (magnification, ×200). (A) Control group, (B) doxorubicin group, (C) L-gossypol group and (D) combination group.

Fluorescence microscopy

Control HSSCs were observed to be condensed, granular and exhibit clear fluorescence in either the nuclei or the cytoplasm following 48 h of treatment (Fig. 3). In addition, apoptosis was clearly evident. The cells shrank, the chromatin became condensed and marginated and clear fragments were observed inside the cytoplasm. The cell membrane was observed to form bubble-like protrusions and apoptotic bodies were formed.

Figure 3 Hoechst 33258 staining illustrating apoptosis of SW982 cells following the action of doxorubicin and L-gossypol (magnification, ×200). (A) Control group, (B) doxorubicin group, (C) L-gossypol group and (D) combination group.

TEM

The results from the TEM demonstrated that the control HSSCs were oval, with a large number of microvilli on the cell surface. The nuclei were clearly visible, the distribution of intranuclear chromatin was uneven and intracytoplasmic mitochondria were common (Fig. 4). Following drug coculture, the cells appeared to morphologically transition to exhibit apoptotic characteristics. These predominantly manifested as disappearance and condensation of the microvilli on the apoptotic cell surface, and the appearance of marginated intranuclear chromatin. Additionally, in the early cellular stages, HSSCs were crescent-shaped, whilst during the late stage the cells swelled and ruptured, the nuclei shrank and fragmented, a large number of vacuoles appeared in the cytoplasm and apoptotic bodies appeared (Fig. 4).

Figure 4 Stages of apoptosis visualized using transmission electron microscopy. (A) Control group, (B) doxorubicin group, (C) L-gossypol group and (D) combination group. In the control group, the structure of cells was normal. In the doxorubicin group and L-gossypol group, cells in the early apoptotic stage and middle apoptotic stage could be observed. In the combination goup, numerous cells were in the late apoptotic stage.

Analysis of apoptosis

Following coculture for 48 h, the early apoptotic rates of L-gossypol and doxorubicin in the experimental groups were 18.40±2.20 and 23.20±2.45%, respectively, which were significantly higher than the control group (4.30±0.26%; P<0.001) (Table III, Fig. 5). The early apoptotic rate of L-gossypol/doxorubicin combination therapy was (38.70±3.40%). No significant interaction between the two drugs was observed (P=0.623), however, a single-factor analysis of variance revealed that the apoptotic rate in the combination group was significantly increased compared with the other groups (P<0.001).

Figure 5 Apoptosis in SW982 cells. (A) Control group, (B) doxorubicin group, (C) combination group and (D) L-gossypol group. Quadrant 4 indicates cells undergoing apoptosis. PI, propidium iodide; FITC, fluorescein isothiocyanate.

Table III Impact analysis of cell apoptosis.

Table III

Impact analysis of cell apoptosis.

Group	Apoptotic rate	ANOVA of factorial design		ANOVA of single factor
		F-ratio	P-value	F-ratio	P-value
Control	4.30±0.26			107.562	<0.001
Doxorubicin	23.20±2.45ac	205.342	<0.001
L-gossypol	18.40±2.20ab	117.082	<0.001
Combination	38.70±3.40abc	0.262	0.623

a P<0.001 vs. the control group;

b P<0.05 vs. the doxorubicin group;

c P<0.01 vs. the L-gossypol group. ANOVA, analysis of variance.

Analysis of cell cycle

The proportion of cells in the G1 phase in the experimental groups increased significantly following 24-h drug treatment (P=0.05 and P<0.001 in the doxorubicin and L-gossypol groups, respectively; Table IV). As presented in Table V, following 48-h coculture, the proportion of L-gossypol group cells in the G1 phase increased to 88.31±1.26%, compared with 80.95±1.61% in the control group (P=0.048). The numbers of cells in the S phase in the doxorubicin group (15.03±1.29%) and the combination group (26.29±1.16%) were also significantly different compared with the control group (9.48±0.65%; P<0.001) and a significant interaction was observed (P<0.001). These results indicate that L-gossypol predominantly arrests the cells in the G1 phase, while doxorubicin and the combination therapy predominantly arrest cells in the S phase (Table IV and V, Fig. 6).

Figure 6 Cell cycles of SW982 cells, analyzed by EXPO 32 MultiComp software. (A) Control group, (B) doxorubicin group, (C) L-gossypol group, (D) combination group.

Table IV Alterations in the cell cycle following drug treatment of SW982 cells for 24 h.

Table IV

Alterations in the cell cycle following drug treatment of SW982 cells for 24 h.

Group	G1	ANOVA of factorial design		G2	S	ANOVA of factorial design
		F-ratio	P-value			F-ratio	P-value
Control	78.56±2.51			7.18±0.93	13.31±2.45
Doxorubicin	83.75±1.48a	5.32	0.05	9.16±1.42	5.53±1.45a	13.77	0.01
L-gossypol	86.32±3.15ab	18.93	<0.001	8.52±2.42	3.90±1.95a	27.39	<0.001
Combination	86.96±0.84a	3.26	0.11	8.32±2.05	3.80±1.56a	13.03	0.01
F-ratio	9.169			0.670	18.063
P-value	0.006			0.594	0.001

a P<0.005 vs. the control group;

b P<0.05 vs. the doxorubicin group; P<0.01 vs. the L-gossypol group. ANOVA, analysis of variance.

Table V Alterations in the cell cycle following drug treatment of SW982 cells for 48 h.

Table V

Alterations in the cell cycle following drug treatment of SW982 cells for 48 h.

Group	G1	ANOVA of factorial design		G2	S	ANOVA of factorial design
		F-ratio	P-value			F-ratio	P-value
Control	80.95±1.61			8.41±0.83	9.48±0.65
Doxorubicin	76.71±1.26a	253.066	<0.001	7.18±0.93	15.03±1.29a	705.678	<0.001
L-gossypol	88.31±1.26ab	5.421	0.048	8.17±1.82	2.79±0.32ab	17.443	0.003
Combination	65.38±1.73abc	119.75	<0.001	7.13±0.74	26.29±1.16abc	269.791	<0.001
F-ratio	126.079			0.978	330.97
P-value	<0.001			0.450	<0.001

a P<0.005 vs. the control group;

b P<0.05 vs. the doxorubicin group;

c P<0.01 vs. the L-gossypol group. ANOVA, analysis of variance.

Bcl-2 and Bax protein expression levels

Bcl-2 protein levels following L-gossypol and doxorubicin coculture (18.30±1.32% and 19.73±2.01%, respectively) were significantly reduced compared with the control group (32.66±1.58%; P<0.001) (Table VI and Fig. 7). In addition, during combination therapy, the levels of Bcl-2 were further reduced (6.43±0.97%) while the interaction of the two drugs was not significant. Furthermore, L-gossypol and doxorubicin produced significant increases in Bax protein levels (18.08±1.46% and 12.36±1.80%) when compared with the control group (4.36±0.60%; P<0.001). Following combination therapy, Bax levels were further increased (25.31±1.41%), however, no significant interaction between the two drugs was observed (P=0.644).

Figure 7 Expression levels of Bcl-2, Bax and β-actin proteins in SW982 cells following 24-h action of doxorubicin. 1, control group; 2, doxorubicin group; 3, L-gossypol group; 4, combination group.

Table VI Alterations in Bcl-2 and Bax protein expression levels following drug treatment of SW982 cells for 24 h.

Table VI

Alterations in Bcl-2 and Bax protein expression levels following drug treatment of SW982 cells for 24 h.

Group	Bcl-2/β-actin (%)	ANOVA of factorial design		Bax/β-actin (%)	ANOVA of factorial design
		F-ratio	P-value		F-ratio	P-value
Control	32.66±1.58			4.36±0.60
Doxorubicin	19.73±2.01a	248.663	<0.001	12.36±1.80a	90.289	<0.001
L-gossypol	18.30±1.32a	199.791	<0.001	18.08±1.46ab	276.769	<0.001
Combination	6.43±0.97abc	0.365	0.562	25.31±1.41abc	0.2317	0.644
F-ratio	149.607			122.43
P-value	<0.001			<0.001

a P<0.005 vs. the control group;

b P<0.001 vs. the doxorubicin group;

c P<0.001 vs. the L-gossypol group. ANOVA, analysis of variance.

Caspase-3 and -9 activity

Significant activation of caspase-9 and -3 in SW982 cells was observed in every treatment group at at least one time point, compared with time point 0 h (P<0.05). Caspase-9 activity reached its maximum value at 6 h subsequent to drug administration. Following 12 h, caspase-9 activity began to decline towards the control level. By contrast, no caspase-3 activity was observed prior to 12 h, and began to reduce at 18 h. The single-factor analysis of variance indicated that the combination group led to a significantly greater increase in caspase activity compared with the L-gossypol group, the doxorubicin group and the control group (P<0.05, Fig. 8). The data also demonstrate that the concentration required to achieve the same inhibitory effect was lower in the combination therapy group (data not shown).

Figure 8 Alterations in levels of (A) caspase-9 and (B) caspase-3 activity at different time points in SW982 cells. *P<0.05, compared with the control group.

Discussion

Apoptosis is controlled by various genes and is a process of programmed death that results in alterations in cellular morphology. These alterations include chromatin condensation and peripheralization, cytoplasm reduction and densification, nuclear fragmentation, interruption of surrounding cell contacts and fusion of endoplasmic reticulum and the cell membrane (16). The result of these morphological alterations is the formation of apoptotic bodies from cell fragmentation. The mitochondrial pathway is vital in apoptosis, and a variety of pro-apoptotic factors act on the mitochondria, leading to the opening of the mitochondrial permeability transition pore. Damage to the outer membrane in turn results in an increased permeability of the mitochondrial membrane, thus resulting in a release of apoptosis-associated molecules, which in turn activate apoptotic factors such as caspase-9 and its downstream factor, caspase-3 (17). This ultimately results in apoptosis. The results of the current study suggest that L-gossypol and/or LCD-induced apoptosis is results from the activation of caspase-9, in addition to downstream caspase-3 activation.

The results of the current study also demonstrated that L-gossypol and LCD therapy resulted in a clear reduction in Bcl-2 and an increase in Bax protein content. In addition, when these two drugs were used in combination therapy, the alterations in Bcl-2 and Bax protein expression levels were observed to be more pronounced. The members of the Bcl-2 family are important in apoptosis and are widely distributed in the outer mitochondrial membrane, nuclear membrane and endoplasmic reticulum. They possess the ability to either inhibit (via Bcl-2), or activate (via Bax) the process of apoptosis. In addition, Bcl-2 has been reported to inhibit the activation of Bax protein (18), isolate or inactivate Bax protein (19,20), form a heterodimer with Bax and inhibit the formation of the Bax/Bax homodimer (21). When the Bax/Bcl-2 heterodimer is formed, Bax loses its ability to alter the permeability of the mitochondrial membrane, and thus cannot induce cellular apoptosis (22–24). Bcl-2 and Bax are part of a dynamic system in which the ratio of Bcl-2/Bax determines whether apoptosis occurs or not (25,26), and this is mediated via caspase-3 (27,28). Therefore, it was hypothesized that L-gossypol and LCD therapies act by altering the ratio of Bcl-2 and Bax protein via a mitochondria-dependent mechanism, which results in the activation of caspase-9. This theory is supported by the observation that combination therapy had a synergistic effect, indicating that these drugs act through the mitochondrial pathway, thus the apoptotic effects are more pronounced when the two drugs are combined.

Cell cycle analysis suggested that L-gossypol blocks cells in the G1 phase, while LCD blocks those in the S phase; and the combination of the two drugs significantly increased the number of cells in the S phase. The regulation of the cell cycle is a complex process, but a previous study indicated the G1/S checkpoint to be an important point during the cell cycle, at which numerous factors can affect the cycle (29). It has been observed that 10 μmol/l gossypol arrested MCF-7 cells at the G1/S checkpoint and inhibited DNA synthesis (30). In addition, gossypol has been identified to reduce the activity of DNA polymerase α and β, inhibit DNA synthesis and block the cell cycle in the S phase, thus indicating gossypol as a specific inhibitor of DNA synthesis (31). Certain studies have reported that gossypol does not appear to alter the cell cycle (32,33), however, these discrepancies are speculated to be due to the impact of gossypol on the cell cycle being cell type-specific, or due to differences among gossypol and its derivatives.

In summary, the current study demonstrated for the first time that L-gossypol and LCD produce significant effects on the inhibition of proliferation and the activation of apoptosis in SW982 HSSCs, and that the combination of the two drugs significantly potentiates these effects. It is hypothesized that the mechanism of action of the two drugs is via downregulation of Bcl-2 protein and upregulation of Bax protein levels, in addition to the impacts of these drugs on the cell cycle of the HSSCs. The results of the current study support the use of L-gossypol in combination with other chemotherapeutic drugs in clinical study. In addition, they provide a preliminary theoretical foundation for the clinical use of LCD, which is hypothesized to reduce the dose required and the resultant side-effects. Further investigation is required to fully elucidate the cellular and molecular mechanisms of L-gossypol therapy and the clinical significance of this.

References