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全球赖氨酸乙酰组分析揭示 CCL18 在非小细胞肺癌中的潜在作用。

Global analysis of lysine acetylome reveals the potential role of CCL18 in non-small cell lung cancer.

机构信息

Department of Biology, School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Department of Clinical Laboratory, Anhui Provincial Hospital, Anhui Medical University, Hefei, 23001, China.

出版信息

Proteomics. 2021 Apr;21(7-8):e2000144. doi: 10.1002/pmic.202000144. Epub 2021 Mar 8.

DOI:10.1002/pmic.202000144
PMID:33570763
Abstract

C-C motif chemokine 18 (CCL18) belongs to the chemokine CC family and is predominantly secreted by M2-tumor-associated macrophages. It has been reported to be associated with various diseases and malignancies. Previous studies showed that CCL18 promotes metastasis by activating downstream kinases. However, it remains unknown whether CCL18 regulates post-translational modifications, other than phosphorylation, during tumorigenesis. Here, we demonstrate that CCL18 is up-regulated in non-small cell lung cancer (NSCLC) and is involved in regulating the lysine acetylome in A549 cells. Using the combination of SILAC labeling and high-efficiency acetylation enrichment methods, we identified 1372 lysine acetylation (Kac) sites on 796 proteins in CCL18-treated A549 cells. Among the identified Kac sites, 147 from 126 proteins were down-regulated and seven from five proteins were up-regulated with fold changes more than two and the p-value less than 0.05. Bioinformatics analysis further showed that the proteins with down-regulated acetylation play critical roles in glycolysis, oxidative phosphorylation, tricarboxylic acid cycle, and pentose phosphate pathway in A549 cells. These results suggest that CCL18 may be involved in the development of NSCLC by regulating acetylation of the proteins in many fundamental cellular processes, especially the metabolic reprogramming of tumor cells.

摘要

C-C motif 趋化因子 18(CCL18)属于趋化因子 CC 家族,主要由 M2-肿瘤相关巨噬细胞分泌。据报道,它与各种疾病和恶性肿瘤有关。先前的研究表明,CCL18 通过激活下游激酶促进转移。然而,CCL18 是否调节肿瘤发生过程中的翻译后修饰(除磷酸化外)尚不清楚。在这里,我们证明 CCL18 在非小细胞肺癌(NSCLC)中上调,并参与调节 A549 细胞中的赖氨酸乙酰化组。使用 SILAC 标记和高效乙酰化富集方法的组合,我们在 CCL18 处理的 A549 细胞中鉴定了 796 个蛋白上的 1372 个赖氨酸乙酰化(Kac)位点。在鉴定的 Kac 位点中,有 147 个来自 126 个蛋白的乙酰化水平下调,7 个来自 5 个蛋白的乙酰化水平上调,倍数变化大于 2,p 值小于 0.05。生物信息学分析进一步表明,下调乙酰化的蛋白在 A549 细胞的糖酵解、氧化磷酸化、三羧酸循环和戊糖磷酸途径中发挥关键作用。这些结果表明,CCL18 可能通过调节许多基本细胞过程中蛋白的乙酰化参与 NSCLC 的发展,特别是肿瘤细胞的代谢重编程。

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