KNK437通过靶向热休克因子1抑制非小细胞肺癌细胞的生长

IF 4.2 4区 医学 Q2 CHEMISTRY, MEDICINAL
Lili Wu, Jieni Feng, Hualong Lin, Peirui Chen
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引用次数: 0

摘要

热休克因子1 (HSF1)已成为多种实体瘤的治疗靶点。然而,其在非小细胞肺癌(NSCLC)中的具体作用以及HSF1抑制剂在此背景下的潜在功效在很大程度上仍未被探索。目前的数据显示,HSF1在NSCLC细胞中过表达,并与NSCLC患者较差的生存结果呈正相关。此外,HSF1抑制剂KNK437显著抑制NSCLC细胞增殖并诱导剂量依赖性细胞周期阻滞和凋亡。此外,KNK437显著改变HSF1过表达NSCLC细胞中HSF1及其下游靶基因的表达,而敲低HSF1可显著减弱KNK437的抗增殖作用,表明其治疗效果主要是通过抑制HSF1介导的。最后,分子对接模拟显示KNK437参与疏水相互作用,并与HSF1形成两个关键氢键,可能支持其抑制活性。总的来说,这些发现支持HSF1作为NSCLC治疗的一个引人注目的分子靶点,并强调KNK437是一个有前途的治疗候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

KNK437 Suppresses the Growth of Non-Small Cell Lung Cancer Cells by Targeting Heat Shock Factor 1

KNK437 Suppresses the Growth of Non-Small Cell Lung Cancer Cells by Targeting Heat Shock Factor 1

KNK437 Suppresses the Growth of Non-Small Cell Lung Cancer Cells by Targeting Heat Shock Factor 1

KNK437 Suppresses the Growth of Non-Small Cell Lung Cancer Cells by Targeting Heat Shock Factor 1

Heat shock factor 1 (HSF1) has emerged as a promising therapeutic target in various solid tumors. However, its specific role in non-small cell lung cancer (NSCLC) and the potential efficacy of HSF1 inhibitors in this context remain largely unexplored. The current data showed that HSF1 is overexpressed in NSCLC cells and is positively associated with poorer survival outcomes in NSCLC patients. Moreover, the HSF1 inhibitor KNK437 markedly suppresses NSCLC cell proliferation and induces dose-dependent cell cycle arrest and apoptosis. In addition, KNK437 significantly alters the expression of HSF1 and its downstream target genes in HSF1-overexpressing NSCLC cells, while HSF1 knockdown markedly attenuates the anti-proliferative effects of KNK437, indicating that its therapeutic efficacy is largely mediated through HSF1 inhibition. Finally, molecular docking simulations revealed that KNK437 engages in hydrophobic interactions and forms two critical hydrogen bonds with HSF1, potentially underpinning its inhibitory activity. Collectively, these findings support HSF1 as a compelling molecular target for NSCLC treatment and highlight KNK437 as a promising therapeutic candidate.

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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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