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硬脂酰辅酶 A 去饱和酶 1 作为癌症的治疗靶点:以肝细胞癌为重点。

Stearoyl-CoA desaturase 1 as a therapeutic target for cancer: a focus on hepatocellular carcinoma.

机构信息

Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Plant Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.

出版信息

Mol Biol Rep. 2022 Sep;49(9):8871-8882. doi: 10.1007/s11033-021-07094-2. Epub 2022 Jul 29.

Abstract

One of the main characteristics of cancer cells is the alteration in lipid composition, which is associated with a significant monounsaturated fatty acids (MUFAs) enrichment. In addition to their structural functions in newly synthesized membranes in proliferating cancer cells, these fatty acids are involved in tumorigenic signaling. Increased expression and activity of stearoyl CoA desaturase (SCD1), i.e., an enzyme converting saturated fatty acids to Δ9-monounsaturated fatty acids, has been observed in various cancer cells. This increase in expression and activity has also been associated with cancer aggressiveness and poor patient outcome. Previous studies have also indicated the SCD1 involvement in increased cancer cells proliferation, growth, migration, epithelial to mesenchymal transition, metastasis, chemoresistance, and maintenance of cancer stem cells properties. Hence, SCD1 seems to be a player in malignancy development and may be considered a novel therapeutic target in cancers, including hepatocellular carcinoma (HCC). This review study aims to discuss the impact of SCD1 as a major component in lipid signaling in HCC.

摘要

癌细胞的一个主要特征是脂质组成的改变,这与单不饱和脂肪酸(MUFAs)的显著富集有关。除了在增殖癌细胞中新合成的膜中的结构功能外,这些脂肪酸还参与肿瘤发生信号。在各种癌细胞中,观察到硬脂酰辅酶 A 去饱和酶(SCD1)的表达和活性增加,即一种将饱和脂肪酸转化为 Δ9-单不饱和脂肪酸的酶。这种表达和活性的增加也与癌症的侵袭性和患者预后不良有关。先前的研究还表明 SCD1 参与了癌细胞增殖、生长、迁移、上皮间质转化、转移、化疗耐药性以及维持癌症干细胞特性的增加。因此,SCD1 似乎是恶性肿瘤发展的一个参与者,并且可能被认为是包括肝细胞癌(HCC)在内的癌症的一个新的治疗靶点。本综述研究旨在讨论 SCD1 作为 HCC 中脂质信号的主要成分的影响。

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