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Effects of the proapoptotic regulator Bcl-2/adenovirus EIB 19-kDa-interacting protein 3 on the chemosensitivity of human colon cancer cell lines

机译:促凋亡调节剂Bcl-2 /腺病毒EIB 19-kDa相互作用蛋白3对人结肠癌细胞株化学敏感性的影响

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摘要

In the clinical setting, drug resistance remains a significant obstacle for successful chemotherapy. Bcl-2/adenovirus EIB 19-kDa-interacting protein 3 (BNIP3) is a proapoptotic member of the Bcl-2 family. To address its potential as a therapeutic target for chemosensitisation, this study investigated the effect of BNIP3 expression on chemosensitivity and reversal of oxaliplatin (L-OHP) resistance in human colon cancer cell lines. A plasmid expressing the BNIP3 gene was transfected into human parental colon cancer cell lines (SW620 and colo320) and L-OHP-resistant colon cancer cell lines (SW620/L-OHP and colo320/L-OHP) using Lipofectamine™ 2000, and the transfection efficiency was determined using fluorescence optics. Western blot analysis identified that SW620/L-OHP and colo320/L-OHP cells expressed lower levels of BNIP3 protein compared with the SW620 and colo320 cells. Transfection with the recombinant BNIP3 plasmid revealed an increase in BNIP3 expression in tumour cells. Following transfection with pDsRed-BNIP3, the chemosensitivity of parental and L-OHP-resistant cell lines to L-OHP was increased (P<0.01), as detected by the Cell Counting Kit-8 (CCK8) assay. Hoechst 33342 staining and flow cytometry revealed that the effects on L-OHP-induced apoptosis were enhanced by the overexpression of BNIP3. Chemosensitisation in human colon cancer cells was observed following treatment with the recombinant BNIP3 plasmid in vitro. The results of this study suggest that BNIP3 is a potential therapeutic target for reversing the resistance of L-OHP-resistant colon cancer cells to L-OHP.
机译:在临床环境中,耐药性仍然是成功化疗的重要障碍。 Bcl-2 /腺病毒EIB 19-kDa相互作用蛋白3(BNIP3)是Bcl-2家族的促凋亡成员。为了解决其作为化学增敏的治疗靶标的潜力,本研究调查了BNIP3表达对人结肠癌细胞株化学敏感性和奥沙利铂(L-OHP)耐药性逆转的影响。使用Lipofectamine™2000将表达BNIP3基因的质粒转染到人亲代结肠癌细胞系(SW620和colo320)和耐L-OHP的结肠癌细胞系(SW620 / L-OHP和colo320 / L-OHP)中,使用荧光光学元件测定转染效率。 Western blot分析表明,与SW620和colo320细胞相比,SW620 / L-OHP和colo320 / L-OHP细胞表达的BNIP3蛋白水平较低。用重组BNIP3质粒转染显示肿瘤细胞中BNIP3表达增加。用pDsRed-BNIP3转染后,亲代和L-OHP耐药细胞系对L-OHP的化学敏感性增加(P <0.01),如通过细胞计数试剂盒8(CCK8)分析所检测。 Hoechst 33342染色和流式细胞仪显示,BNIP3的过表达增强了对L-OHP诱导的细胞凋亡的作用。在体外用重组BNIP3质粒处理后,观察到人结肠癌细胞的化学增敏作用。这项研究的结果表明,BNIP3是逆转L-OHP耐药结肠癌细胞对L-OHP的耐药性的潜在治疗靶标。

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