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通过抑制TRAIL敏感和TRAIL耐药结肠癌细胞中的促生存途径对TRAIL诱导的细胞凋亡进行不同调节。

Different modulation of TRAIL-induced apoptosis by inhibition of pro-survival pathways in TRAIL-sensitive and TRAIL-resistant colon cancer cells.

作者信息

Vaculová Alena, Hofmanová Jirina, Soucek Karel, Kozubík Alois

机构信息

Laboratory of Cytokinetics, Institute of Biophysics, Academy of Sciences of the Czech Republic, Královopolská 135, 612 65 Brno, Czech Republic.

出版信息

FEBS Lett. 2006 Dec 11;580(28-29):6565-9. doi: 10.1016/j.febslet.2006.11.004. Epub 2006 Nov 13.

Abstract

Epithelial cells can be manipulated to undergo apoptosis depending on the balance between pro-survival and apoptotic signals. We showed that TRAIL-induced apoptosis may be differentially regulated by inhibitors of MEK ERK (U0126) or PI3K/Akt (LY294002) pathway in TRAIL-sensitive (HT-29) and TRAIL-resistant (SW620) human epithelial colon cancer cells. U0126 or LY294002 significantly enhanced TRAIL-induced apoptosis in HT-29 cells, but not in SW620 cells. We report a different regulation of the level of an anti-apoptotic Mcl-1 protein under MEK/ERK or PI3K/Akt pathway inhibition and suggest the mechanisms involved. A special attention was paid to the role of the ERK1/2, Akt, and glycogen synthase kinase 3beta.

摘要

上皮细胞可根据生存信号和凋亡信号之间的平衡被操控而发生凋亡。我们发现,在对TRAIL敏感的(HT - 29)和对TRAIL耐药的(SW620)人结肠上皮癌细胞中,TRAIL诱导的凋亡可能受到MEK ERK(U0126)或PI3K/Akt(LY294002)信号通路抑制剂的不同调控。U0126或LY294002显著增强了TRAIL诱导的HT - 29细胞凋亡,但对SW620细胞无此作用。我们报道了在MEK/ERK或PI3K/Akt信号通路抑制下抗凋亡蛋白Mcl - 1水平的不同调控情况,并提出了相关机制。特别关注了ERK1/2、Akt和糖原合酶激酶3β的作用。

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