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N6-甲基腺苷修饰的 circPAK2 通过靶向 IGF2BPs/VEGFA 信号通路促进胃癌淋巴结转移。

N6-methyladenosine modified circPAK2 promotes lymph node metastasis via targeting IGF2BPs/VEGFA signaling in gastric cancer.

机构信息

The Third Department of Surgery, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Hebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang, Hebei, China.

出版信息

Oncogene. 2024 Aug;43(34):2548-2563. doi: 10.1038/s41388-024-03099-w. Epub 2024 Jul 17.

Abstract

Circular RNAs (circRNAs) have emerged as key regulators of cancer occurrence and progression, as well as promising biomarkers for cancer diagnosis and prognosis. However, the potential mechanisms of circRNAs implicated in lymph node (LN) metastasis of gastric cancer remain unclear. Herein, we identify a novel N6-methyladenosine (m6A) modified circRNA, circPAK2, which is significantly upregulated in gastric cancer tissues and metastatic LN tissues. Functionally, circPAK2 enhances the migration, invasion, lymphangiogenesis, angiogenesis, epithelial-mesenchymal transition (EMT), and metastasis of gastric cancer in vitro and in vivo. Mechanistically, circPAK2 is exported by YTH domain-containing protein 1 (YTHDC1) from the nucleus to the cytoplasm in an m6A methylation-dependent manner. Moreover, increased cytoplasmic circPAK2 interacts with Insulin-Like Growth Factor 2 mRNA-Binding Proteins (IGF2BPs) and forms a circPAK2/IGF2BPs/VEGFA complex to stabilize VEGFA mRNA, which contributes to gastric cancer vasculature formation and aggressiveness. Clinically, high circPAK2 expression is positively associated with LN metastasis and poor prognosis in gastric cancer. This study highlights m6A-modified circPAK2 as a key regulator of LN metastasis of gastric cancer, thus supporting circPAK2 as a promising therapeutic target and prognostic biomarker for gastric cancer.

摘要

环状 RNA(circRNAs)已成为癌症发生和发展的关键调节因子,也是癌症诊断和预后有前途的生物标志物。然而,circRNAs 在胃癌淋巴结转移中所涉及的潜在机制尚不清楚。在此,我们鉴定出一种新型 N6-甲基腺苷(m6A)修饰的环状 RNA,circPAK2,其在胃癌组织和转移性淋巴结组织中显著上调。功能上,circPAK2 增强了胃癌在体外和体内的迁移、侵袭、淋巴管生成、血管生成、上皮-间充质转化(EMT)和转移。机制上,circPAK2 依赖 m6A 甲基化由 YTH 结构域包含蛋白 1(YTHDC1)从细胞核输出到细胞质。此外,增加的细胞质 circPAK2 与胰岛素样生长因子 2 mRNA 结合蛋白(IGF2BPs)相互作用,并形成 circPAK2/IGF2BPs/VEGFA 复合物来稳定 VEGFA mRNA,这有助于胃癌血管生成和侵袭性。临床上,高 circPAK2 表达与胃癌的淋巴结转移和预后不良呈正相关。这项研究强调了 m6A 修饰的 circPAK2 是胃癌淋巴结转移的关键调节因子,因此支持 circPAK2 作为胃癌有前途的治疗靶点和预后生物标志物。

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