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缺氧巨噬细胞中的HIF-1α/IL-8轴通过增强PD-L1表达促进食管癌进展。

HIF-1α/IL-8 axis in hypoxic macrophages promotes esophageal cancer progression by enhancing PD-L1 expression.

作者信息

Song Shuai, Zhang Yahui, Duan Xinchun, Liu Chunquan, Du Yanlin, Wang Xiaoran, Luo Yi, Cui Yong

机构信息

Department of Thoracic Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

Department of Pharmacy, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.

出版信息

Cancer Gene Ther. 2023 Feb;30(2):358-367. doi: 10.1038/s41417-022-00551-5. Epub 2022 Nov 10.

Abstract

Esophageal cancer (EC) is a malignancy with poor prognosis and high mortality. Hypoxic microenvironment has also been proved to be an important feature of tumors. Herein, we mainly studied the influence of hypoxia-treated tumor-associated macrophages (TAMs) on EC malignant phenotype and related molecular mechanism. In this paper, we found that hypoxic macrophages contributed to EC cell proliferation, cell cycle progression, and metastasis. Besides, the hypoxia treatment expedited the transformation of macrophages into M2 polarization. The level of interleukin (IL)-8 was boosted in macrophages after hypoxia treatment. Moreover, hypoxia treatment heightened IL-8 secretion by macrophages via positively regulating hypoxia-inducible factor-1α (HIF-1α) expression. The IL-8 secreted by hypoxic macrophages facilitated EC cell proliferation, cell cycle progression, and metastasis by elevating ligand of programmed death 1 (PD-L1) expression. In the end, IL-8 also expedited EC tumorigenesis in vivo. In conclusion, HIF-1α/IL-8 axis in hypoxic macrophages could expedite EC advancement by upregulating PD-L1 level, which might deliver a novel thought for EC cure.

摘要

食管癌(EC)是一种预后差、死亡率高的恶性肿瘤。缺氧微环境也已被证明是肿瘤的一个重要特征。在此,我们主要研究了缺氧处理的肿瘤相关巨噬细胞(TAM)对EC恶性表型的影响及相关分子机制。在本文中,我们发现缺氧巨噬细胞促进了EC细胞增殖、细胞周期进程和转移。此外,缺氧处理加速了巨噬细胞向M2极化的转变。缺氧处理后巨噬细胞中白细胞介素(IL)-8水平升高。而且,缺氧处理通过正向调节缺氧诱导因子-1α(HIF-1α)表达提高了巨噬细胞的IL-8分泌。缺氧巨噬细胞分泌的IL-8通过提高程序性死亡1(PD-L1)配体表达促进EC细胞增殖、细胞周期进程和转移。最后,IL-8在体内也加速了EC肿瘤发生。总之,缺氧巨噬细胞中的HIF-1α/IL-8轴可通过上调PD-L1水平加速EC进展,这可能为EC治疗提供新思路。

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