TRIM14通过己胺生物合成途径抑制非小细胞肺癌的进展。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-05-19 DOI:10.1093/carcin/bgae005
Sisi Wei, Meiling Ai, Yuan Zhan, Jieqing Yu, Tao Xie, Qinghua Hu, Yang Fang, Xuan Huang, Yong Li
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引用次数: 0

摘要

TRIM14 (Tripartite Motif 14)是一种属于E3连接酶TRIM家族的肿瘤蛋白,它参与了除非小细胞肺癌(NSCLC)以外的多种肿瘤的进展。然而,目前人们对 TRIM14 在 NSCLC 中的功能和相关机制知之甚少。在这里,我们发现与邻近组织相比,TRIM14 蛋白在肺腺癌组织中下调,它可以抑制肿瘤细胞在体外和体内的增殖和迁移。此外,TRIM14 可直接与谷氨酰胺果糖-6-磷酸酰胺基转移酶 1(GFAT1)结合,进而导致 GFAT1 降解和 O 型糖基化水平降低。GFAT1 是己胺生物合成途径(HBP)限速步骤中的一个关键酶。补充 N-乙酰-D-葡糖胺可以成功逆转 TRIM14 对 NSCLC 细胞生长和迁移的抑制作用。总之,我们的数据揭示了TRIM14通过泛素化和降解GFAT1抑制NSCLC细胞的增殖和迁移,为TRIM14在HBP上提供了新的调控作用。
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TRIM14 suppressed the progression of NSCLC via hexosamine biosynthesis pathway.

Tripartite Motif 14 (TRIM14) is an oncoprotein that belongs to the E3 ligase TRIM family, which is involved in the progression of various tumors except for non-small cell lung carcinoma (NSCLC). However, little is currently known regarding the function and related mechanisms of TRIM14 in NSCLC. Here, we found that the TRIM14 protein was downregulated in lung adenocarcinoma tissues compared with the adjacent tissues, which can suppress tumor cell proliferation and migration both in vitro and in vivo. Moreover, TRIM14 can directly bind to glutamine fructose-6-phosphate amidotransferase 1 (GFAT1), which in turn results in the degradation of GFAT1 and reduced O-glycosylation levels. GFAT1 is a key enzyme in the rate-limiting step of the hexosamine biosynthetic pathway (HBP). Replenishment of N-acetyl-d-glucosamine can successfully reverse the inhibitory effect of TRIM14 on the NSCLC cell growth and migration as expected. Collectively, our data revealed that TRIM14 suppressed NSCLC cell proliferation and migration through ubiquitination and degradation of GFAT1, providing a new regulatory role for TRIM14 on HBP.

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CiteScore
7.20
自引率
4.30%
发文量
567
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