超级增强子MYCNOS-SE通过招募转录因子CTCF和KLF15促进小细胞肺癌的化疗耐药性。

IF 6.9 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Oncogene Pub Date : 2024-11-08 DOI:10.1038/s41388-024-03202-1
Yuchun Niu, Yichun Tang, Feng Ma, Xuyang Zhou, Yi Chen, Yu Wang, Yue Xu, Lei Sun, Shaoqiang Liang, Jianqi Yang, Kai Wang, Fan Zhang, Shan Su, Linlang Guo
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引用次数: 0

摘要

小细胞肺癌(SCLC)是一种侵袭性肺癌,通常会对化疗产生耐药性。了解化疗耐药的分子机制对于确定有效的治疗靶点至关重要。在本研究中,我们利用 RNA-Seq 鉴定了与化疗耐药性相关的高表达分子。我们还进行了H3K27Ac和ATAC-Seq结合分析,以确定超级增强子(SE)及其相应的转录因子。我们进行了体外和体内实验来研究这些分子的影响,并收集了临床样本来确定它们的预后价值。我们的研究结果表明,MYCNOS表达升高,在体外和体内SCLC模型中均表现出化疗抗性。我们发现MYCNOS-SE是SCLC中一个重要的SE,它调控远端靶基因MYCNOS。该SE招募转录因子CTCF和KLF15来调控MYCNOS的表达。此外,研究还发现 MYCN 的反义 MYCNOS 可通过 NOTCH 通路调节化疗敏感性。这项研究强调了SE调节的靶基因作为SCLC化疗耐药性标志物的重要性。此外,该研究还表明,MYCNOS可作为一种预测因子来识别可能从NOTCH抑制剂中获益的患者。这些发现为今后研究开发针对这些已确定通路的治疗策略提供了宝贵的见解。
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Super-enhancer MYCNOS-SE promotes chemoresistance in small cell lung cancer by recruiting transcription factors CTCF and KLF15.

Small cell lung cancer (SCLC) is an aggressive form of lung cancer that often becomes resistant to chemotherapy. Understanding the molecular mechanisms of chemoresistance is crucial for identifying effective therapeutic targets. In this study, we used RNA-Seq to identify highly expressed molecules associated with chemoresistance. We also performed H3K27Ac and ATAC-Seq binding analyses to identify super-enhancers (SE) and their corresponding transcription factors. Both in vitro and in vivo experiments were conducted to examine the impact of these molecules and clinical samples were collected to establish their prognostic value. Our findings revealed elevated expression of MYCNOS, which exhibited chemoresistant properties in both in vitro and in vivo models of SCLC. We identified MYCNOS-SE as a significant SE in SCLC that regulates the distal target gene MYCNOS. This SE recruits transcription factors CTCF and KLF15 to regulate MYCNOS expression. Additionally, MYCNOS, an antisense of MYCN, was found to modulate chemotherapy sensitivity through the NOTCH pathway. This study highlights the significance of SE -regulated target genes as markers for chemoresistance in SCLC. Furthermore, it suggests that MYCNOS could serve as a predictor to identify patients who may benefit from NOTCH inhibitors. These findings provide valuable insights for future studies aimed at developing therapeutic strategies targeting these identified pathways.

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来源期刊
Oncogene
Oncogene 医学-生化与分子生物学
CiteScore
15.30
自引率
1.20%
发文量
404
审稿时长
1 months
期刊介绍: Oncogene is dedicated to advancing our understanding of cancer processes through the publication of exceptional research. The journal seeks to disseminate work that challenges conventional theories and contributes to establishing new paradigms in the etio-pathogenesis, diagnosis, treatment, or prevention of cancers. Emphasis is placed on research shedding light on processes driving metastatic spread and providing crucial insights into cancer biology beyond existing knowledge. Areas covered include the cellular and molecular biology of cancer, resistance to cancer therapies, and the development of improved approaches to enhance survival. Oncogene spans the spectrum of cancer biology, from fundamental and theoretical work to translational, applied, and clinical research, including early and late Phase clinical trials, particularly those with biologic and translational endpoints.
期刊最新文献
Super-enhancer MYCNOS-SE promotes chemoresistance in small cell lung cancer by recruiting transcription factors CTCF and KLF15. Correction: AR loss in prostate cancer stroma mediated by NF-κB and p38-MAPK signaling disrupts stromal morphogen production. Editorial Expression of Concern: 5-Aza-2'-deoxycytidine and IFN-γ cooperate to sensitize for TRAIL-induced apoptosis by upregulating caspase-8. EphA2 regulates vascular permeability and prostate cancer metastasis via modulation of cell junction protein phosphorylation. Nuclear versus cytoplasmic IKKα signaling in keratinocytes leads to opposite skin phenotypes and inflammatory responses, and a different predisposition to cancer.
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