LncRNA-MALAT1 mediates cisplatin resistance via miR-101-3p/VEGF-C pathway in bladder cancer

作者: Peihua Liu , Xiaozhou Li , Yu Cui , Jinbo Chen , Chao Li

DOI: 10.1093/ABBS/GMZ112

关键词:

摘要: Cisplatin (CDDP)-based chemotherapy is a standard strategy for the clinical treatment of patients with bladder cancer (BC). However, anti-tumor efficacy cisplatin affected by multiple chemoresistance complex molecular mechanisms. Recent evidence highlights crucial regulatory roles metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) in progression cancers and development drug resistance. underlying mechanisms MALAT1 resistance BC cells remain largely unclear. In this study, we firstly demonstrated that expression was up-regulated tissues compared to normal adjacent elevated epithelial immortalized cells. Secondly, found suppression enhanced chemotherapeutic sensitivity inhibited Thirdly, showed via regulating miR-101-3p/VEGF-C pathway. summary, study demonstrates MALAT1, miR-101-3p VEGF-C form axis affect chemo-resistance CDDP, provides novel potential targets BC.

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