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缺氧诱导的自噬有助于肝癌细胞的化疗耐药性。

Hypoxia-induced autophagy contributes to the chemoresistance of hepatocellular carcinoma cells.

机构信息

Tumor Immunology and Gene Therapy Center, Eastern Hepatobiliary Surgery Hospital, The Second Military Medical University, Shanghai, China.

出版信息

Autophagy. 2009 Nov;5(8):1131-44. doi: 10.4161/auto.5.8.9996. Epub 2009 Nov 4.

Abstract

Hypoxia commonly exists in solid tumors. Under such adverse conditions, adaptive responses including autophagy are usually provoked to promote cell survival. In our study, autophagy, a lysosomal-mediated degradation pathway, is demonstrated as a protective way to make hepatocellular carcinoma cells resistant to chemotherapy under hypoxia. Compared with normoxia, chemotherapeutic agent-induced cell death under hypoxia was significantly decreased, as a result of the reduced apoptosis. However, when autophagy was inhibited by 3-MA or siRNA targeted Beclin 1, this reduction was reversed, i.e., chemoresistance was attenuated, which means autophagy mediates the chemoresistance under hypoxia. In conclusion, autophagy decreases hepatoma cells sensitization to chemotherapeutic agents by affecting their apoptotic potential.

摘要

缺氧通常存在于实体肿瘤中。在这种不利条件下,通常会引发包括自噬在内的适应性反应,以促进细胞存活。在我们的研究中,自噬是一种溶酶体介导的降解途径,被证明是一种保护机制,可以使肝癌细胞在缺氧环境下对化疗产生抗性。与常氧相比,缺氧条件下化疗药物诱导的细胞死亡明显减少,这是由于凋亡减少的结果。然而,当自噬被 3-MA 或靶向 Beclin 1 的 siRNA 抑制时,这种减少被逆转,即耐药性减弱,这意味着自噬介导了缺氧下的耐药性。总之,自噬通过影响肝癌细胞的凋亡潜能来降低其对化疗药物的敏感性。

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