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Enhanced anticancer effect of ABT-737 in combination with naringenin on gastric cancer cells

机译:ABT-737结合柚皮苷对胃癌细胞的增强抗癌作用

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摘要

Gastric cancer is the second leading cause of cancer-associated mortality and is a frequently occurring cancer worldwide. Multiple drug resistance of gastric cancer cells leads to the poor prognosis. In addition, overexpression of anti-apoptotic protein B-cell lymphoma (Bcl)-2 have been demonstrated in various cancer cells and is closely associated with drug resistance and poor prognosis. Naringenin is a flavonoid that has antimutagenic and anticarcinogenic activities in numerous cancer types. In the present study, naringenin and a Bcl-2 inhibitor, ABT-737, were used to investigate their combinative anticancer effect in the SGC7901 gastric cancer cell line. The results revealed that naringenin and ABT-737 were able to inhibit SGC7901 cell growth and colony formation, alone or in combination. Furthermore, the combination of these drugs was found to further increase the cleavage of caspase-3 and poly ADP-ribose polymerase. Naringenin and ABT-737 also decreased Akt activation and increased p53 expression, suggesting the involvement of these pathways in the inhibition of gastric cell growth.
机译:胃癌是与癌症相关的死亡率的第二大主要原因,并且是全世界范围内经常发生的癌症。胃癌细胞的多重耐药性导致预后不良。此外,已在多种癌细胞中证明了抗凋亡蛋白B细胞淋巴瘤(Bcl)-2的过表达,并且与耐药性和不良预后密切相关。柚皮素是一种类黄酮,在多种癌症类型中均具有抗突变和抗癌活性。在本研究中,柚皮苷和Bcl-2抑制剂ABT-737用于研究其在SGC7901胃癌细胞系中的联合抗癌作用。结果表明,柚皮素和ABT-737能够单独或组合抑制SGC7901细胞的生长和集落形成。此外,发现这些药物的组合进一步增加了对caspase-3和聚ADP-核糖聚合酶的切割。柚皮素和ABT-737还可降低Akt激活并增加p53表达,表明这些途径参与了胃细胞生长的抑制。

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