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Published on: June 18, 2015
Mangosteen Inhibits Growth and Survival of Cervical Cancer Cells
Nathan T Givens1, Lei Zhao2, Ziwen Zhu3
1Department of Microbiology, Immunology and Pathology, Des Moines University, Des Moines, IA, U.S.A.
Background:
Cervical cancer is the most common cancer of the female reproductive system. Late-stage cervical cancer treatment has been largely unsuccessful, and urgent anti-cancer therapy is needed. Mangosteen, a tropical fruit, has been studied and found to be rich in xanthones, known anti-cancer compounds. This study was designed to investigate the effect of mangosteen extract (ME) on SiHa cervical cancer cells and to explore the underlying molecular mechanisms.
Materials And Methods:
Clonogenic survival assay, Quick Cell Proliferation Assay, terminal deoxynucleotidyl transferase biotin-dUTP nick end labeling (TUNEL) staining, and caspase-3 activity kits were used to investigate the in vitro role of ME treatment in SiHa cervical cancer cell growth. We further investigated the possible molecular mechanisms using RT-PCR. Statistical analysis was done with unpaired two-tailed Student's t-test and significance at p-value <0.05; each experiment was repeated three times.
Results:
Our study found that the growth and proliferation of SiHa cervical cancer cells was inhibited by ME. ME also induced apoptosis in SiHa cervical cancer cells. The anti-proliferative effect of ME on cervical cancer cells was associated with statistically significant (p<0.05) down-regulation of the pro-proliferative molecules cyclin B, cyclin D and cyclin E. The pro-apoptotic effect of ME was associated with statistically significant (p<0.05) down-regulation of the anti-apoptotic molecules flice-like inhibitory protein (FLIP) and survivin.
Conclusion:
ME impedes the growth and survival of SiHa cervical cancer cells by down-regulating cyclin B, cyclin D, cyclin E as well as FLIP and survivin. ME may be a promising strategy for targeted cancer immunotherapy development.
Insights
Mangosteen extract (ME) inhibits cervical cancer cell growth and survival by down-regulating key cell cycle and apoptosis-related molecules. This suggests ME as a potential candidate for novel cancer immunotherapy development.
Area of Science:
- Oncology
- Pharmacology
- Natural Products Research
Background:
- Cervical cancer remains a significant health concern, particularly in late stages where treatment efficacy is limited.
- There is an urgent need for novel anti-cancer therapies.
- Mangosteen, a tropical fruit, contains xanthones with known anti-cancer properties.
Purpose of the Study:
- To investigate the anti-cancer effects of mangosteen extract (ME) on SiHa cervical cancer cells.
- To explore the molecular mechanisms underlying ME's action.
Main Methods:
- In vitro assays including clonogenic survival, cell proliferation, TUNEL staining, and caspase-3 activity were employed.
- Gene expression analysis using RT-PCR investigated molecular targets.
- Statistical significance was determined using Student's t-test (p<0.05).
Main Results:
- Mangosteen extract (ME) significantly inhibited the growth and proliferation of SiHa cervical cancer cells.
- ME treatment induced apoptosis in these cancer cells.
- Down-regulation of pro-proliferative cyclins (B, D, E) and anti-apoptotic proteins (FLIP, survivin) was observed.
Conclusions:
- Mangosteen extract (ME) effectively impedes cervical cancer cell growth and survival.
- The mechanism involves the down-regulation of cyclins B, D, E, FLIP, and survivin.
- ME shows promise as a potential therapeutic strategy for developing targeted cancer immunotherapies.
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