MYC家族扩增决定了小细胞肺癌患者对BET溴域蛋白抑制剂Mivebresib(ABBV-075)的敏感性。

IF 4.1 2区 医学 Q2 CELL BIOLOGY Molecular Cancer Research Pub Date : 2024-08-02 DOI:10.1158/1541-7786.MCR-23-0599
Joshua P Plotnik, Zheng Zha, Weiguo Feng, Irene Lee, Jacob Riehm, Ryan A McClure, Stephanie Sandoval, Tamar Uziel, Erin Murphy, Xin Lu, Lloyd T Lam
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引用次数: 0

摘要

小细胞肺癌(SCLC)占所有肺癌的近 15%。虽然患者对一线治疗反应迅速,但很快复发是不可避免的,二线治疗选择很少。在这里,我们描述了MYC和MYCN扩增的SCLC细胞系,但不包括MYCL1和非扩增的MYC细胞系,它们对泛BET溴域蛋白抑制剂Mivebresib(ABBV-075)的治疗表现出更高的敏感性。沉默MYC和MYCN可部分缓解Mivebresib的抗增殖作用,从而挽救携带这些各自扩增的SCLC细胞系。对 MYC、MYCN 和 MYCL1 的全基因组结合的进一步鉴定发现了独特的增强子和表观遗传学偏好。意义:我们的研究表明,染色质景观可以建立具有独特基因表达程序的细胞状态,从而传递对米韦布瑞布等表观遗传抑制剂的敏感性。
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MYC Family Amplification Dictates Sensitivity to BET Bromodomain Protein Inhibitor Mivebresib (ABBV075) in Small-Cell Lung Cancer.

Small-cell lung cancer (SCLC) accounts for nearly 15% of all lung cancers. Although patients respond to first-line therapy readily, rapid relapse is inevitable, with few treatment options in the second-line setting. Here, we describe SCLC cell lines harboring amplification of MYC and MYCN but not MYCL1 or non-amplified MYC cell lines exhibit superior sensitivity to treatment with the pan-BET bromodomain protein inhibitor mivebresib (ABBV075). Silencing MYC and MYCN partially rescued SCLC cell lines harboring these respective amplifications from the antiproliferative effects of mivebresib. Further characterization of genome-wide binding of MYC, MYCN, and MYCL1 uncovered unique enhancer and epigenetic preferences. Implications: Our study suggests that chromatin landscapes can establish cell states with unique gene expression programs, conveying sensitivity to epigenetic inhibitors such as mivebresib.

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来源期刊
Molecular Cancer Research
Molecular Cancer Research 医学-细胞生物学
CiteScore
9.90
自引率
0.00%
发文量
280
审稿时长
4-8 weeks
期刊介绍: Molecular Cancer Research publishes articles describing novel basic cancer research discoveries of broad interest to the field. Studies must be of demonstrated significance, and the journal prioritizes analyses performed at the molecular and cellular level that reveal novel mechanistic insight into pathways and processes linked to cancer risk, development, and/or progression. Areas of emphasis include all cancer-associated pathways (including cell-cycle regulation; cell death; chromatin regulation; DNA damage and repair; gene and RNA regulation; genomics; oncogenes and tumor suppressors; signal transduction; and tumor microenvironment), in addition to studies describing new molecular mechanisms and interactions that support cancer phenotypes. For full consideration, primary research submissions must provide significant novel insight into existing pathway functions or address new hypotheses associated with cancer-relevant biologic questions.
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