| Literature DB >> 24877693 |
Fang-fang Zhang1, Yi-fei Zhu1, Qian-nan Zhao1, Dan-tong Yang1, Ye-ping Dong1, Li Jiang1, Wei-xing Xing1, Xi-yuan Li1, Hui Xing1, Mei Shi1, Yun Chen1, Iain C Bruce1, Jian Jin2, Xin Ma3.
Abstract
The overexpression of P-glycoprotein (P-gp) causes resistance to chemotherapy in human ovarian cancer. However, the underlying mechanism remains unclear. In the present study, we showed that, at membrane-bound protein level, P-gp was 'shared' between human ovarian cancer cells by the intercellular transfer of microvesicles (MVs). Paclitaxel-resistant human ovarian cancer cells (A2780/PTX) readily formed and released P-gp-containing MVs into the extracellular space compared with the wild-type parental line (A2780/WT). Shedding MVs bound to the chemosensitive A2780/WT cells in a time- and dose-dependent manner, transferring P-gp via the microenvironment. MV-mediated transfer of P-gp led to redistribution of the chemotherapeutic drug adriamycin in recipient cells (A2780/WT), which displayed 5- and 5-fold higher resistance to adriamycin and paclitaxel, respectively. Thus, these findings demonstrate a new mechanism of drug-resistance acquisition via MVs.Entities:
Keywords: Adriamycin (PubChem CID: 31703); Human ovarian cancer cells; Intercellular transfer; Microvesicles; P-glycoprotein; Paclitaxel (PubChem CID:36314)
Mesh:
Substances:
Year: 2014 PMID: 24877693 DOI: 10.1016/j.ejphar.2014.05.026
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432