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促红细胞生成素诱导的肝细胞受体A2调节细胞焦亡对胃肠道结直肠癌发生和转移抗性的影响。

Erythropoietin-induced hepatocyte receptor A2 regulates effect of pyroptosis on gastrointestinal colorectal cancer occurrence and metastasis resistance.

作者信息

Zhang Yu-Kun, Shi Ran, Meng Ruo-Yu, Lin Shui-Li, Zheng Mei

机构信息

Department of Rehabilitation Medicine, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan 250014, Shandong Province, China.

Department of Minimally Invasive Comprehensive Treatment of Cancer, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250021, Shandong Province, China.

出版信息

World J Gastrointest Oncol. 2024 Sep 15;16(9):3781-3797. doi: 10.4251/wjgo.v16.i9.3781.

Abstract

Erythropoietin-induced hepatocyte receptor A2 (EphA2) is a receptor tyrosine kinase that plays a key role in the development and progression of a variety of tumors. This article reviews the expression of EphA2 in gastrointestinal (GI) colorectal cancer (CRC) and its regulation of pyroptosis. Pyroptosis is a form of programmed cell death that plays an important role in tumor suppression. Studies have shown that EphA2 regulates pyrodeath through various signaling pathways, affecting the occurrence, development and metastasis of GI CRC. The overexpression of EphA2 is closely related to the aggressiveness and metastasis of GI CRC, and the inhibition of EphA2 can induce pyrodeath and improve the sensitivity of cancer cells to treatment. In addition, EphA2 regulates intercellular communication and the microenvironment through interactions with other cytokines and receptors, further influencing cancer progression. The role of EphA2 in GI CRC and its underlying mechanisms provide us with new perspectives and potential therapeutic targets, which have important implications for future cancer treatment.

摘要

促红细胞生成素诱导的肝细胞受体A2(EphA2)是一种受体酪氨酸激酶,在多种肿瘤的发生和发展中起关键作用。本文综述了EphA2在胃肠道(GI)结直肠癌(CRC)中的表达及其对细胞焦亡的调控。细胞焦亡是一种程序性细胞死亡形式,在肿瘤抑制中起重要作用。研究表明,EphA2通过多种信号通路调节细胞焦亡,影响胃肠道结直肠癌的发生、发展和转移。EphA2的过表达与胃肠道结直肠癌的侵袭性和转移密切相关,抑制EphA2可诱导细胞焦亡并提高癌细胞对治疗的敏感性。此外,EphA2通过与其他细胞因子和受体相互作用调节细胞间通讯和微环境,进一步影响癌症进展。EphA2在胃肠道结直肠癌中的作用及其潜在机制为我们提供了新的视角和潜在的治疗靶点,对未来癌症治疗具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4221/11438782/583cab494634/WJGO-16-3781-g001.jpg

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