Pristimerin overcomes adriamycin resistance in breast cancer cells through suppressing Akt signaling
Author(s) -
Guie Xie,
Xinpei Yu,
Huichao Liang,
Jingsong Chen,
Xuewei Tang,
Shaoqing Wu,
Can Liao
Publication year - 2016
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2016.4335
Subject(s) - cancer , breast cancer , cancer research , medicine , oncogene , apoptosis , cancer cell , doxorubicin , chemotherapy , protein kinase b , multiple drug resistance , downregulation and upregulation , mcf 7 , drug resistance , pharmacology , cell cycle , biology , human breast , biochemistry , gene , microbiology and biotechnology
Breast cancer remains a major public health problem worldwide. Chemotherapy serves an important role in the treatment of breast cancer. However, resistance to chemotherapeutic agents, in particular, multi-drug resistance (MDR), is a major cause of treatment failure in cancer. Agents that can either enhance the effects of chemotherapeutics or overcome chemoresistance are urgently needed for the treatment of breast cancer. Pristimerin, a quinonemethide triterpenoid compound isolated from Celastraceae and Hippocrateaceae, has been shown to possess antitumor, anti-inflammatory, antioxidant and insecticidal properties. The aim of the present study was to investigate whether pristimerin can override chemoresistance in MCF-7/adriamycin (ADR)-resistant human breast cancer cells. The results demonstrated that pristimerin indeed displayed potent cytocidal effect on multidrug-resistant MCF-7/ADR breast cancer cells, and that these effects occurred through the suppression of Akt signaling, which in turn led to the downregulation of antiapoptotic effectors and increased apoptosis. These findings indicate that use of pristimerin may represent a potentially promising approach for the treatment of ADR-resistant breast cancer.
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