RESEARCH ARTICLE |
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Year : 2016 | Volume
: 48
| Issue : 6 | Page : 637-642 |
Genistein synergizes centchroman action in human breast cancer cells
Shweta Kaushik1, Hari Shyam2, Ramesh Sharma3, Anil K Balapure1
1 Division of Biochemistry, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh; Academy of Scientific and Innovative Research (AcSIR), Taramani, Chennai, Tamil Nadu, India 2 Division of Biochemistry, CSIR-Central Drug Research Institute; Centre for Advance Research, King George's Medical University, Lucknow, Uttar Pradesh, India 3 Division of Biochemistry, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India
Correspondence Address:
Anil K Balapure Division of Biochemistry, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh; Academy of Scientific and Innovative Research (AcSIR), Taramani, Chennai, Tamil Nadu India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0253-7613.194852
Objectives: Despite the progress in the diagnosis and treatment of breast cancer, it remains a major health problem in women. Natural flavones along with chemotherapeutic agents enhance therapeutic response and minimize toxicity of chemical agents. Centchroman (CC) colloquially called as ormeloxifene, is a nonsteroidal oral contraceptive categorized as selective estrogen receptor modulator with anti-breast cancer activity. Genistein (GN), an isoflavone found mainly in soy products possesses anti-cancerous potential against a number of cancers including breast. The present study aims at investigating the combination of CC and GN in human breast cancer cell lines (HBCCs).
Materials and Methods: Cytotoxic effect of CC and GN separately and in combination were assessed by sulforhodamine B (SRB) assay in MDA MB-231, MDA MB-468, MCF-7, T-47D HBCCs, and nontumorigenic human mammary epithelial cell (HMEC) MCF-10A. The drug interaction was analyzed using CompuSyn software through which combination index and dose reduction index were generated.
Results: Combination of CC plus GN exerts significantly higher cytotoxicity compared to each drug per se in HBCCs, whereas HMEC-MCF-10A remains unaffected.
Conclusion: On an overall basis, the drugs in combination enhanced cell killing in malignant cells. Therefore, the combination of CC with GN may offer a novel approach for the breast cancer.
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