李卫华, 杨佳欣. 硬脂酰辅酶A去饱和酶1与恶性肿瘤的研究进展[J]. 中国肿瘤临床, 2014, 41(17): 1131-1134. DOI: 10.3969/j.issn.1000-8179.20140483
引用本文: 李卫华, 杨佳欣. 硬脂酰辅酶A去饱和酶1与恶性肿瘤的研究进展[J]. 中国肿瘤临床, 2014, 41(17): 1131-1134. DOI: 10.3969/j.issn.1000-8179.20140483
LI Weihua, YANG Jiaxin. Development in the study of the correlation between stearoyl-coenzyme A desaturase 1 and cancer progression[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2014, 41(17): 1131-1134. DOI: 10.3969/j.issn.1000-8179.20140483
Citation: LI Weihua, YANG Jiaxin. Development in the study of the correlation between stearoyl-coenzyme A desaturase 1 and cancer progression[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2014, 41(17): 1131-1134. DOI: 10.3969/j.issn.1000-8179.20140483

硬脂酰辅酶A去饱和酶1与恶性肿瘤的研究进展

Development in the study of the correlation between stearoyl-coenzyme A desaturase 1 and cancer progression

  • 摘要: 由于耐药性的产生和化疗药物的毒副反应,恶性肿瘤的化疗效果一直不满意。为了寻找新的、选择性的抗肿瘤药物,人们对肿瘤细胞的代谢异常作了大量研究。越来越多的研究发现,肿瘤组织的恶性生物学行为与其特殊的物质代谢和能量代谢密切相关。增殖迅速的肿瘤细胞的一个代谢特点为脂质生成增多。硬脂酰辅酶A去饱和酶1(Stearoyl-coenzyme A desaturase 1,SCD1)是催化饱和脂肪酸向单不饱和脂肪酸转变的限速酶,与肥胖、脂肪性肝脏病变、胰岛素抵抗等一系列的代谢综合征及癌症的发生、发展密切相关。研究SCD1在恶性肿瘤中的作用将为肿瘤患者化疗提供新的治疗靶点。

     

    Abstract: The curative effect of chemotherapy in malignant tumors has been unsatisfactory because of drug resistance and the toxicity of chemotherapeutic drugs. Extensive studies on the metabolism of tumor cells have been undertaken to determine a novel selective antitumor drug. An increasing number of studies have demonstrated the close relation between the malignant behavior of tumor tissues and their specialized energy metabolism. Hyper-lipogenesis is one of the metabolic characteristics of the rapid proliferation of tumor cells. Stearoyl-coenzyme A desaturase 1 (SCD1) is a critical enzyme in fatty acid synthesis because it catalyzes the conversion of saturated fatty acids into monounsaturated fatty acids. This enzyme is closely related to obesity, fatty liver disease, insulin resistance, and a series of metabolic syndromes. It is also involved in the occurrence and progression of cancer. Determining the function of SCD1 in malignant tumors would provide a new therapeutic target in chemotherapy.

     

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