抑制真核启动因子 4E 可预防化疗引起的脱发。

IF 2.9 3区 医学 Q2 Medicine
Zeina Nasr, Lukas E Dow, Marilene Paquet, Jennifer Chu, Kontham Ravindar, Ragam Somaiah, Pierre Deslongchamps, John A Porco, Scott W Lowe, Jerry Pelletier
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引用次数: 0

摘要

背景:化疗引起的脱发(alopecia)(CIA)是癌症患者最担心的化疗副作用之一。目前还没有一种药理方法可以最大限度地减轻 CIA,不过已经提出的一种策略是通过短暂诱导细胞周期停滞来保护正常细胞免受化疗的影响。这种方法被称为 "周期疗法"(cyclotherapy),其概念已在细胞培养环境中得到证实:方法:真核生物起始因子(eIF)4E 是一种帽结合蛋白,在翻译的起始阶段刺激核糖体招募到 mRNA 模板。已知抑制 eIF4E 可诱导细胞周期停滞。我们利用一种新型的可诱导和可逆的转基因小鼠模型,在体内实现了 RNAi- 介导的 eIF4E 抑制,评估了时间性 eIF4E 抑制对 CIA 的影响:结果:我们的研究结果表明,瞬时抑制 eIF4E 可在机体水平上防止环磷酰胺诱导的脱发。在细胞水平上,这种保护作用与细胞在 G1 期的积累、凋亡指数的降低有关,并且与针对翻译启动过程的小分子抑制剂的表型相似:我们的数据为探索抑制翻译起始作为预防或减少环磷酰胺诱发脱发的方法提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Suppression of eukaryotic initiation factor 4E prevents chemotherapy-induced alopecia.

Suppression of eukaryotic initiation factor 4E prevents chemotherapy-induced alopecia.

Suppression of eukaryotic initiation factor 4E prevents chemotherapy-induced alopecia.

Suppression of eukaryotic initiation factor 4E prevents chemotherapy-induced alopecia.

Background: Chemotherapy-induced hair loss (alopecia) (CIA) is one of the most feared side effects of chemotherapy among cancer patients. There is currently no pharmacological approach to minimize CIA, although one strategy that has been proposed involves protecting normal cells from chemotherapy by transiently inducing cell cycle arrest. Proof-of-concept for this approach, known as cyclotherapy, has been demonstrated in cell culture settings.

Methods: The eukaryotic initiation factor (eIF) 4E is a cap binding protein that stimulates ribosome recruitment to mRNA templates during the initiation phase of translation. Suppression of eIF4E is known to induce cell cycle arrest. Using a novel inducible and reversible transgenic mouse model that enables RNAi-mediated suppression of eIF4E in vivo, we assessed the consequences of temporal eIF4E suppression on CIA.

Results: Our results demonstrate that transient inhibition of eIF4E protects against cyclophosphamide-induced alopecia at the organismal level. At the cellular level, this protection is associated with an accumulation of cells in G1, reduced apoptotic indices, and was phenocopied using small molecule inhibitors targeting the process of translation initiation.

Conclusions: Our data provide a rationale for exploring suppression of translation initiation as an approach to prevent or minimize cyclophosphamide-induced alopecia.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACY-TOXICOLOGY
CiteScore
4.40
自引率
0.00%
发文量
0
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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