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星形细胞上调基因 1(AEG-1)通过诱导肝癌细胞自噬促进了失巢凋亡抵抗和转移。

Astrocyte elevated gene 1 (AEG-1) promotes anoikis resistance and metastasis by inducing autophagy in hepatocellular carcinoma.

机构信息

Division of Gastroenterology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Cell Physiol. 2020 Jun;235(6):5084-5095. doi: 10.1002/jcp.29377. Epub 2019 Nov 6.

Abstract

Astrocyte elevated gene 1 (AEG-1) is overexpressed in hepatocellular carcinoma (HCC) and is strongly associated with tumor metastasis. Anoikis resistance and autophagy may play an important role in the survival of circulating tumor cells. However, the relationship among AEG-1, anoikis resistance, autophagy, and metastasis in HCC is still not clear. The results of this study indicate that AEG-1 expression is increased in HCC cell lines grown in suspension culture. AEG-1 could enhance anoikis resistance to promote the survival of detached HCC cells. Moreover, the anoikis resistance appears to be partly dependent on autophagy. Regulating AEG-1 expression changed the autophagy levels to modulate anoikis resistance, likely acting via the protein kinase RNA-like ER kinase (PERK)-eIF2α-ATF4-CHOP signaling axis. Finally, inhibiting autophagy by RNA interference prevented the AEG-1-promoted metastasis of HCC xenografts to the liver and lungs of nude mice. Taken together, AEG-1 is a key contributor to anoikis resistance and metastasis by inducing autophagy in vitro and in vivo, and it may be a potential target for therapeutic intervention in HCC.

摘要

星形细胞上调基因 1(AEG-1)在肝细胞癌(HCC)中过表达,与肿瘤转移强烈相关。无锚定生存和自噬可能在循环肿瘤细胞的存活中发挥重要作用。然而,AEG-1、抗失巢凋亡、自噬与 HCC 转移之间的关系尚不清楚。本研究结果表明,在悬浮培养中生长的 HCC 细胞系中 AEG-1 的表达增加。AEG-1 可增强抗失巢凋亡作用,促进脱落 HCC 细胞的存活。此外,抗失巢凋亡似乎部分依赖于自噬。调节 AEG-1 的表达可改变自噬水平来调节抗失巢凋亡,可能通过蛋白激酶 RNA 样内质网激酶(PERK)-eIF2α-ATF4-CHOP 信号通路发挥作用。最后,RNA 干扰抑制自噬可防止 AEG-1 促进 HCC 异种移植物在裸鼠肝脏和肺部的转移。综上所述,AEG-1 通过体外和体内诱导自噬促进抗失巢凋亡和转移,是 HCC 治疗干预的潜在靶点。

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