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饮食中海油酸诱导 CD36 通过上调Src/ERK 通路促进宫颈癌的生长和转移。

Dietary oleic acid-induced CD36 promotes cervical cancer cell growth and metastasis via up-regulation Src/ERK pathway.

机构信息

Centre for Lipid Research & Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.

John Moorhead Research Laboratory, Centre for Nephrology, University College London Medical School, Royal Free Campus, University College London, London, NW3 2PF, United Kingdom.

出版信息

Cancer Lett. 2018 Dec 1;438:76-85. doi: 10.1016/j.canlet.2018.09.006. Epub 2018 Sep 11.

Abstract

Epidemiological and experimental studies have revealed strong associations between dietary lipids and cancer risk. However, the molecular mechanisms underlying the effects of dietary fatty acids on the genesis and progression of cancer have been poorly explored. In this study, we found that a high olive oil diet stimulated cervical cancer (CC) carcinogenesis, and oleic acid (OA), the main lipid in olive oil, was associated with increased malignancy in HeLa cells. OA up-regulated the expression of CD36, which is the best characterized fatty acid transporter. Inhibiting CD36 prevented the tumor-promoting effects of OA, while overexpressing CD36 mimicked the effects of OA. Clinically, CD36 expression was positively correlated with tumor progression and poor prognosis in patients with CC. Furthermore, OA induced Src kinase and downstream ERK1/2 pathway activation in a CD36-dependent manner. Pretreatment of HeLa cells with an Src kinase inhibitor largely blocked the tumor-promoting effect of OA. Our findings suggest that dietary OA exerts a stimulatory effect on CC growth and metastasis, and CD36 might be a promising therapeutic target that acts against CC through an Src/ERK-dependent signaling pathway.

摘要

流行病学和实验研究表明,膳食脂质与癌症风险之间存在很强的关联。然而,饮食脂肪酸对癌症发生和发展的影响的分子机制还未被充分探索。在这项研究中,我们发现高橄榄油饮食会刺激宫颈癌(CC)的发生,而橄榄油中的主要脂质——油酸(OA)与 HeLa 细胞恶性程度的增加有关。OA 上调了 CD36 的表达,CD36 是最具特征的脂肪酸转运蛋白。抑制 CD36 可预防 OA 的促瘤作用,而过表达 CD36 则模拟了 OA 的作用。临床上,CC 患者的 CD36 表达与肿瘤进展和预后不良呈正相关。此外,OA 以 CD36 依赖的方式诱导 Src 激酶和下游 ERK1/2 通路的激活。用Src 激酶抑制剂预处理 HeLa 细胞可显著阻断 OA 的促瘤作用。我们的研究结果表明,膳食 OA 对 CC 的生长和转移具有刺激作用,CD36 可能是一种有前途的治疗靶点,通过 Src/ERK 依赖性信号通路发挥抗 CC 作用。

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