Liu Danyang, Hu Yang, Guo Ying, Zhu Zhu, Lu Bingzheng, Wang Xuelan, Huang Yijun
Department of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
State Key Laboratory of Oncology in South China, Collaborative Innovation Centre for Cancer Medicine, Sun Yat-sen University Cancer Centre, Guangzhou, China.
PLoS One. 2017 Oct 4;12(10):e0184578. doi: 10.1371/journal.pone.0184578. eCollection 2017.
Mycoplasma infection has been reported to be associated with cancer migration, invasion, epithelial-mesenchymal transition as well as the resistance to nucleoside analogues chemotherapeutic drugs. In this study, we found that the sensitivity of hepatocarcinoma cells to Cisplatin, Gemcitabine and Mitoxantrone was increased by mycoplasma elimination. Similar to the effect of anti-mycoplasma agent, interrupting the interaction between Mycoplasma hyorhinis membrane protein P37 and Annexin A2 of host cells using the N-terminal of ANXA2 polypeptide enhanced the sensitivity of HCC97L cells to Gemcitabine and Mitoxantrone. Meanwhile, we did not observe any changes in expression or distribution of multidrug resistance associated transporters, ATP-Binding Cassette protein B1, C1 and G2, on the removal of mycoplasma. These results suggest that mycoplasma induces a resistance to multiple drugs in hepatocarcinoma cells which required the interaction of P37 and Annexin A2. The pathway downstream this interaction needs to be explored.
据报道,支原体感染与癌症迁移、侵袭、上皮-间质转化以及对核苷类似物化疗药物的耐药性有关。在本研究中,我们发现消除支原体可提高肝癌细胞对顺铂、吉西他滨和米托蒽醌的敏感性。与抗支原体剂的作用类似,使用ANXA2多肽的N端中断猪鼻支原体膜蛋白P37与宿主细胞膜联蛋白A2之间的相互作用,可增强HCC97L细胞对吉西他滨和米托蒽醌的敏感性。同时,在消除支原体后,我们未观察到多药耐药相关转运蛋白ATP结合盒蛋白B1、C1和G2的表达或分布有任何变化。这些结果表明,支原体诱导肝癌细胞对多种药物产生耐药性,这需要P37与膜联蛋白A2的相互作用。这种相互作用下游的途径有待探索。