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囊性纤维化跨膜传导调节因子(CFTR)在发育、分化、再生和癌症中扮演什么角色?

What Role Does CFTR Play in Development, Differentiation, Regeneration and Cancer?

机构信息

BioISI-Biosystems and Integrative Sciences Institute, Faculty of Sciences, University of Lisboa, 1749-016 Lisboa, Portugal.

出版信息

Int J Mol Sci. 2020 Apr 29;21(9):3133. doi: 10.3390/ijms21093133.

DOI:10.3390/ijms21093133
PMID:32365523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7246864/
Abstract

One of the key features associated with the substantial increase in life expectancy for individuals with CF is an elevated predisposition to cancer, firmly established by recent studies involving large cohorts. With the recent advances in cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies and the increased long-term survival rate of individuals with cystic fibrosis (CF), this is a novel challenge emerging at the forefront of this disease. However, the mechanisms linking dysfunctional CFTR to carcinogenesis have yet to be unravelled. Clues to this challenging open question emerge from key findings in an increasing number of studies showing that CFTR plays a role in fundamental cellular processes such as foetal development, epithelial differentiation/polarization, and regeneration, as well as in epithelial-mesenchymal transition (EMT). Here, we provide state-of-the-art descriptions on the moonlight roles of CFTR in these processes, highlighting how they can contribute to novel therapeutic strategies. However, such roles are still largely unknown, so we need rapid progress in the elucidation of the underlying mechanisms to find the answers and thus tailor the most appropriate therapeutic approaches.

摘要

与 CF 患者预期寿命显著延长相关的一个关键特征是癌症易感性增加,这一观点已被最近涉及大量队列的研究证实。随着囊性纤维化跨膜电导调节因子(CFTR)调节剂治疗的最新进展以及囊性纤维化(CF)患者的长期生存率提高,这是该疾病前沿出现的一个新挑战。然而,将功能失调的 CFTR 与致癌作用联系起来的机制仍有待阐明。越来越多的研究显示 CFTR 在胎儿发育、上皮分化/极化和再生以及上皮-间充质转化(EMT)等基本细胞过程中发挥作用,为解决这一具有挑战性的开放性问题提供了线索。在这里,我们提供了 CFTR 在这些过程中扮演的“月光”角色的最新描述,强调了它们如何为新的治疗策略做出贡献。然而,这些作用在很大程度上仍然未知,因此我们需要在阐明潜在机制方面取得快速进展,以找到答案,从而制定最合适的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61b9/7246864/ef173a8d6494/ijms-21-03133-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61b9/7246864/1f6f601a13de/ijms-21-03133-g001.jpg
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Acta Clin Belg. 2021 Oct;76(5):379-380. doi: 10.1080/17843286.2020.1737780. Epub 2020 Mar 5.
3
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