[通过 HER2 信号调控肿瘤微环境--来自异质性 HER2 过度表达胃癌病例的启示]。

Q4 Medicine
Shotaro Nakajima, Satoshi Fukai, Akinao Kaneta, Hideaki Tsumuraya, Akira Matsuishi, Hirokazu Okayama, Motonobu Saito, Kosaku Mimura, Wataru Sakamoto, Zenichiro Saze, Tomoyuki Momma, Koji Kono
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引用次数: 0

摘要

HER2是人类表皮生长因子受体(HER)家族的成员之一,在13%-27%的胃癌病例中,HER2会出现基因扩增、蛋白过表达或两者兼而有之的情况。通过激活下游的 Akt 和 ERK 通路,HER2 促进了胃癌细胞的生存和增殖。HER2信号转导对胃癌肿瘤微环境(TME)的影响仍不清楚,而胃癌组织中HER2过表达的异质性被认为是一个诱因。在这项研究中,我们重点研究了 HER2 阳性 GC 中 HER2 阳性区域和 HER2 阴性区域的肿瘤微环境差异,发现 HER2 信号转导,尤其是 HER2-Akt 级联,可能会抑制干扰素基因刺激因子(STING)的表达,并减少 CD8+ T 细胞在肿瘤细胞中的浸润。总之,我们的研究结果表明,HER2 阳性 GC 有可能采用一种新的治疗方法来激活抗肿瘤免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Regulation of the Tumor Microenvironment through HER2 Signaling-Insights from Gastric Cancer Cases with Heterogeneous HER2 Overexpression].

HER2, a member of the human epidermal growth factor receptor(HER)family, exhibits gene amplification, protein overexpression, or both in 13-27% of gastric cancer(GC)cases. Through the activation of downstream Akt and ERK pathways, HER2 promotes the survival and proliferation of gastric cancer cells. The impact of HER2 signaling on the tumor microenvironment(TME)in GC remains unclear, and the heterogeneity of HER2 overexpression in GC tissues is considered a contributing factor. In this study, we focused on differences in the TME between HER2-positive and HER2-negative areas in HER2-positive GC and found that HER2 signaling, particularly the HER2-Akt cascade, may suppress stimulator of interferon genes (STING)expression and reduce CD8+ T cell infiltration in tumor cells. Overall, our findings suggest the potential for a novel therapeutic approach to activate the anti-tumor immune response in HER2-positive GC.

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