| Literature DB >> 34344693 |
Triantafyllia Karakousi1, Allison L Richards2, Metamia Ciampricotti3,4, Àlvaro Quintanal-Villalonga3,4, Angeliki Karatza5, Rebecca Caeser3,4, Emily A Costa6, Viola Allaj3,4, Parvathy Manoj3,4, Kyle B Spainhower7, Faruk E Kombak8, Francisco J Sanchez-Rivera9, Janneke E Jaspers10, Anastasia-Maria Zavitsanou1, Danilo Maddalo9, Andrea Ventura9, William M Rideout11, Elliot H Akama-Garren11, Tyler Jacks11, Mark T A Donoghue2, Triparna Sen3,4, Trudy G Oliver7, John T Poirier5, Thales Papagiannakopoulos1,5, Charles M Rudin3,4.
Abstract
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. ©2021 American Association for Cancer Research.Entities:
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Year: 2021 PMID: 34344693 PMCID: PMC8810895 DOI: 10.1158/2159-8290.CD-21-0441
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272