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乙酰辅酶A羧化酶:癌症治疗的一个靶点?

The acetyl-CoA carboxylase enzyme: a target for cancer therapy?

作者信息

Wang Chao, Ma Jun, Zhang Nan, Yang Qianlan, Jin Yue, Wang Yu

机构信息

Department of OB&GYN, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200127, China.

出版信息

Expert Rev Anticancer Ther. 2015 Jun;15(6):667-76. doi: 10.1586/14737140.2015.1038246. Epub 2015 May 15.

Abstract

As a rate-limiting enzyme, the acetyl-CoA carboxylase (ACC) is essential for fatty acid synthesis. Traditionally, the ACC has been a target of metabolic syndrome and obesity. Recent research has demonstrated that malignant tumors have a high energy flow, thus having a great ability to synthesize fatty acids. ACCs are occasionally found to be overexpressed in cancer cells, and using chemical or RNA interference to inhibit ACC can lead to cancer cell cycle arrest and apoptosis. This suggests that ACC and relative fatty acids may be critical for the survival of cancer cells. In this review, we summarize the role of ACC in tumor development. We also discuss the signaling pathways possibly affected by ACC, which may give insight into future research for cancer therapy.

摘要

作为一种限速酶,乙酰辅酶A羧化酶(ACC)对于脂肪酸合成至关重要。传统上,ACC一直是代谢综合征和肥胖症的靶点。最近的研究表明,恶性肿瘤具有高能量流,因此具有很强的脂肪酸合成能力。ACC偶尔会在癌细胞中过度表达,使用化学或RNA干扰抑制ACC会导致癌细胞周期停滞和凋亡。这表明ACC和相关脂肪酸可能对癌细胞的存活至关重要。在这篇综述中,我们总结了ACC在肿瘤发展中的作用。我们还讨论了可能受ACC影响的信号通路,这可能为未来的癌症治疗研究提供思路。

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