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Rlf-Mycl 基因融合驱动小细胞肺癌小鼠模型的肿瘤发生和转移。

Rlf-Mycl Gene Fusion Drives Tumorigenesis and Metastasis in a Mouse Model of Small Cell Lung Cancer.

机构信息

Department of Medicine, Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York.

Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Cancer Discov. 2021 Dec 1;11(12):3214-3229. doi: 10.1158/2159-8290.CD-21-0441.

Abstract

UNLABELLED

Small cell lung cancer (SCLC) has limited therapeutic options and an exceptionally poor prognosis. Understanding the oncogenic drivers of SCLC may help define novel therapeutic targets. Recurrent genomic rearrangements have been identified in SCLC, most notably an in-frame gene fusion between RLF and MYCL found in up to 7% of the predominant ASCL1-expressing subtype. To explore the role of this fusion in oncogenesis and tumor progression, we used CRISPR/Cas9 somatic editing to generate a Rlf-Mycl-driven mouse model of SCLC. RLF-MYCL fusion accelerated transformation and proliferation of murine SCLC and increased metastatic dissemination and the diversity of metastatic sites. Tumors from the RLF-MYCL genetically engineered mouse model displayed gene expression similarities with human RLF-MYCL SCLC. Together, our studies support RLF-MYCL as the first demonstrated fusion oncogenic driver in SCLC and provide a new preclinical mouse model for the study of this subtype of SCLC.

SIGNIFICANCE

The biological and therapeutic implications of gene fusions in SCLC, an aggressive metastatic lung cancer, are unknown. Our study investigates the functional significance of the in-frame RLF-MYCL gene fusion by developing a Rlf-Mycl-driven genetically engineered mouse model and defining the impact on tumor growth and metastasis. This article is highlighted in the In This Issue feature, p. 2945.

摘要

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小细胞肺癌(SCLC)的治疗选择有限,预后极差。了解 SCLC 的致癌驱动因素可能有助于确定新的治疗靶点。在 SCLC 中已经确定了反复发生的基因组重排,最显著的是在高达 7%的主要表达 ASCL1 的亚型中发现的 RLF 和 MYCL 之间的框内基因融合。为了探讨这种融合在致癌作用和肿瘤进展中的作用,我们使用 CRISPR/Cas9 体细胞编辑生成了 Rlf-Mycl 驱动的 SCLC 小鼠模型。Rlf-MYCL 融合加速了小鼠 SCLC 的转化和增殖,并增加了转移性扩散和转移性部位的多样性。来自 Rlf-MYCL 基因工程小鼠模型的肿瘤显示出与人类 RLF-MYCL SCLC 相似的基因表达。总之,我们的研究支持 RLF-MYCL 作为 SCLC 中第一个被证实的融合致癌驱动基因,并为研究这种 SCLC 亚型提供了一种新的临床前小鼠模型。

意义

基因融合在侵袭性转移性肺癌 SCLC 中的生物学和治疗意义尚不清楚。我们通过开发 Rlf-Mycl 驱动的基因工程小鼠模型研究了框内 RLF-MYCL 基因融合的功能意义,并确定了其对肿瘤生长和转移的影响。本文在本期特色文章中重点介绍,第 2945 页。

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