Inhibition of ERN1 Signaling is Important for the Suppression of Tumor Growth

O. Minchenko, D. O. Tsymbal, Olena O. Khita, D. Minchenko
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Abstract

Endoplasmic reticulum to nucleus signaling 1 (ERN1) is a major signaling pathway of endoplasmic reticulum stress and is crucial for malignant tumor growth The article aims to discuss the recent progress in the discovery of endoplasmic reticulum stress targets and their involvement in tumor growth. Literature from the PubMed database related to the endoplasmic reticulum stress involvement in the tumor growth and chemoresistance was searched and reviewed. The endoplasmic reticulum stress plays an important part in malignant tumor growth and is involved in invasion and metastasis. Inhibition of protein kinase and endoribonuclease activities of the ERN1 signaling protein significantly reduces tumor growth through down-regulation of angiogenesis and cell proliferation but activates the invasion. ERN1 knockdown affects the expression of many genes associated with the regulation of apoptosis, cell proliferation and survival as well as reprograms the hypoxic regulation of most gene expressions. Simultaneously, inhibition of ERN1 endoribonuclease only has a stronger suppressive effect on tumor growth and decreases the invasiveness.. Present review summarizes the recent advances in the inhibition of ERN1 signaling that regulates tumor growth. Further understanding of the regulatory mechanisms of genome reprogramming upon inhibition of ERN1 signaling may help to discover new possibilities for developing novel effective therapeutics.
抑制ERN1信号传导对抑制肿瘤生长很重要
内质网-细胞核信号传导1(ERN1)是内质网应激的主要信号通路,对恶性肿瘤的生长至关重要。本文旨在讨论近年来内质网应激靶点的发现及其与肿瘤生长的关系。检索并回顾了PubMed数据库中与内质网应激参与肿瘤生长和化疗耐药性有关的文献。内质网应激在恶性肿瘤的生长和侵袭转移中起着重要作用。ERN1信号蛋白的蛋白激酶和核糖核酸内切酶活性的抑制通过下调血管生成和细胞增殖显著降低肿瘤生长,但激活侵袭。ERN1敲低影响许多与细胞凋亡、细胞增殖和存活调节相关的基因的表达,并重新编程大多数基因表达的缺氧调节。同时,抑制ERN1核糖核酸内切酶仅对肿瘤生长具有更强的抑制作用,并降低了侵袭性。。本文综述了近年来抑制调节肿瘤生长的ERN1信号传导的研究进展。进一步了解ERN1信号传导抑制时基因组重编程的调控机制可能有助于发现开发新的有效治疗方法的新可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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