4.6

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2.2

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  • ISSN 1674-8301
  • CN 32-1810/R
Kuppusamy Periyasamy, Venkatachalam Sivabalan, Kuppusamy Baskaran, Kannayiram Kasthuri, Dhanapal Sakthisekaran. Cellular metabolic energy modulation by tangeretin in 7,12-dimethylbenz(a) anthracene-induced breast cancer[J]. The Journal of Biomedical Research, 2016, 30(2): 134-141. DOI: 10.7555/JBR.30.20150060
Citation: Kuppusamy Periyasamy, Venkatachalam Sivabalan, Kuppusamy Baskaran, Kannayiram Kasthuri, Dhanapal Sakthisekaran. Cellular metabolic energy modulation by tangeretin in 7,12-dimethylbenz(a) anthracene-induced breast cancer[J]. The Journal of Biomedical Research, 2016, 30(2): 134-141. DOI: 10.7555/JBR.30.20150060

Cellular metabolic energy modulation by tangeretin in 7,12-dimethylbenz(a) anthracene-induced breast cancer

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the University Grants Commission, New Delhi, in the form of UGC-BSR Research Fellowship under the UGC-SAP-DRS-III programme is gratefully acknowledged

More Information
  • Received Date: April 03, 2015
  • Revised Date: June 01, 2015
  • Breast cancer is the leading cause of death among women worldwide. Chemoprevention and chemotherapy play beneficial roles in reducing the incidence and mortality of cancer. Epidemiological and experimental studies showed that naturally-occurring antioxidants present in the diet may act as anticancer agents. Identifying the abnormalities of cellular energy metabolism facilitates early detection and management of breast cancer. The present study evaluated the effect of tangeretin on cellular metabolic energy fluxes in 7,12-dimethylbenz(a) anthracene (DMBA)-induced proliferative breast cancer. The results showed that the activities of glycolytic enzymes significantly increased in mammary tissues of DMBA-induced breast cancer bearing rats. The gluconeogenic tricarboxylic acid (TCA) cycle and respiratory chain enzyme activities significantly decreased in breast cancer-bearing rats. In addition, proliferating cell nuclear antigen (PCNA) was highly expressed in breast cancer tissues. However, the activities of glycolytic enzymes were significantly normalized in the tangeretin pre- and post-treated rats and the TCA cycle and respiratory chain enzyme activities were significantly increased in tangeretin treated rats. Furthermore, tangeretin down-regulated PCNA expression on breast cancerbearing rats. Our study demonstrates that tangeretin specifically regulates cellular metabolic energy fluxes in DMBA-induced breast cancer-bearing rats.
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