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暴露于甲状旁腺素相关蛋白的结直肠癌细胞生长抑制的潜在治疗靶点。

Potential therapeutic targets for growth arrest of colorectal cancer cells exposed to PTHrP.

机构信息

Instituto de Ciencias Biológicas y Biomédicas del Sur (INBIOSUR), Dept. Biología Bioquímica y Farmacia, Universidad Nacional del Sur-CONICET, Bahía Blanca, Argentina.

Dept. Biología Bioquímica y Farmacia, Universidad Nacional del Sur, Bahía Blanca, Argentina.

出版信息

Mol Cell Endocrinol. 2018 Dec 15;478:32-44. doi: 10.1016/j.mce.2018.07.005. Epub 2018 Jul 21.

Abstract

Although PTHrP is implicated in several cancers, its role in chemoresistance is not fully elucidated. We found that in CRC cells, PTHrP exerts proliferative and protective effects and induces cell migration. The aim of this work was to further study the effects of PTHrP in CRC cells. Herein we evidenced, for the first time, that PTHrP induces resistance to CPT-11 in Caco-2 and HCT116 cells; although both cell lines responded to the drug through different molecular mechanisms, the chemoresistance by PTHrP in these models is mediated through ERK, which in turn is activated by PCK, Src and Akt. Moreover, continue administration of PTHrP in nude mice xenografts increased the protein levels of this MAPK and of other markers related to tumorigenic events. The understanding of the molecular mechanisms leading to ERK 1/2 activation and the study of ERK targets may facilitate the development of new therapeutic strategies for CRC treatment.

摘要

虽然甲状旁腺素相关蛋白 (PTHrP) 与多种癌症有关,但它在化疗耐药中的作用尚未完全阐明。我们发现,在 CRC 细胞中,PTHrP 发挥增殖和保护作用,并诱导细胞迁移。本工作的目的是进一步研究 PTHrP 在 CRC 细胞中的作用。在此,我们首次证明 PTHrP 诱导 Caco-2 和 HCT116 细胞对 CPT-11 的耐药性;尽管这两种细胞系通过不同的分子机制对药物产生反应,但这两种模型中 PTHrP 的化疗耐药性是通过 ERK 介导的,ERK 又被 PCK、Src 和 Akt 激活。此外,在裸鼠异种移植瘤中继续给予 PTHrP 会增加这种 MAPK 和其他与肿瘤发生事件相关的标志物的蛋白水平。了解导致 ERK1/2 激活的分子机制以及研究 ERK 的靶点可能有助于开发 CRC 治疗的新治疗策略。

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