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应激伴侣蛋白GRP78/BiP在转基因诱导的乳腺肿瘤发生发展中对肿瘤增殖、存活及肿瘤血管生成的关键作用

Critical role of the stress chaperone GRP78/BiP in tumor proliferation, survival, and tumor angiogenesis in transgene-induced mammary tumor development.

作者信息

Dong Dezheng, Ni Min, Li Jianze, Xiong Shigang, Ye Wei, Virrey Jenilyn J, Mao Changhui, Ye Risheng, Wang Miao, Pen Ligaya, Dubeau Louis, Groshen Susan, Hofman Florence M, Lee Amy S

机构信息

Department of Biochemistry and Molecular Biology, University of Southern California/Norris Comprehensive Cancer Center, Keck School of Medicine, Los Angeles, California 90089-9176, USA.

出版信息

Cancer Res. 2008 Jan 15;68(2):498-505. doi: 10.1158/0008-5472.CAN-07-2950.

Abstract

The unfolded protein response (UPR) is an evolutionarily conserved mechanism that activates both proapoptotic and survival pathways to allow eukaryotic cells to adapt to endoplasmic reticulum (ER) stress. Although the UPR has been implicated in tumorigenesis, its precise role in endogenous cancer remains unclear. A major UPR protective response is the induction of the ER chaperone GRP78/BiP, which is expressed at high levels in a variety of tumors and confers drug resistance in both proliferating and dormant cancer cells. To determine the physiologic role of GRP78 in in situ-generated tumor and the consequence of its suppression on normal organs, we used a genetic model of breast cancer in the Grp78 heterozygous mice where GRP78 expression level was reduced by about half, mimicking anti-GRP78 agents that achieve partial suppression of GRP78 expression. Here, we report that Grp78 heterozygosity has no effect on organ development or antibody production but prolongs the latency period and significantly impedes tumor growth. Our results reveal three major mechanisms mediated by GRP78 for cancer progression: enhancement of tumor cell proliferation, protection against apoptosis, and promotion of tumor angiogenesis. Importantly, although partial reduction of GRP78 in the Grp78 heterozygous mice substantially reduces the tumor microvessel density, it has no effect on vasculature of normal organs. Our findings establish that a key UPR target GRP78 is preferably required for pathophysiologic conditions, such as tumor proliferation, survival, and angiogenesis, underscoring its potential value as a novel therapeutic target for dual antitumor and antiangiogenesis activity.

摘要

未折叠蛋白反应(UPR)是一种进化上保守的机制,它激活促凋亡和生存途径,使真核细胞能够适应内质网(ER)应激。尽管UPR与肿瘤发生有关,但其在内源性癌症中的精确作用仍不清楚。UPR的一种主要保护反应是诱导内质网伴侣蛋白GRP78/BiP,它在多种肿瘤中高表达,并赋予增殖期和静止期癌细胞耐药性。为了确定GRP78在原位生成肿瘤中的生理作用及其抑制对正常器官的影响,我们使用了Grp78杂合小鼠的乳腺癌遗传模型,其中GRP78表达水平降低了约一半,模拟了实现GRP78表达部分抑制的抗GRP78药物。在此,我们报告Grp78杂合性对器官发育或抗体产生没有影响,但延长了潜伏期并显著阻碍了肿瘤生长。我们的结果揭示了GRP78介导癌症进展的三种主要机制:增强肿瘤细胞增殖、保护细胞免受凋亡以及促进肿瘤血管生成。重要的是,尽管Grp78杂合小鼠中GRP78的部分降低显著降低了肿瘤微血管密度,但对正常器官的脉管系统没有影响。我们的研究结果表明,一个关键的UPR靶点GRP78在病理生理条件下,如肿瘤增殖、生存和血管生成中是优选必需的,突出了其作为具有双重抗肿瘤和抗血管生成活性的新型治疗靶点的潜在价值。

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