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CD74-NRG1 Fusions in Lung Adenocarcinoma

Authors :
Dirk Brehmer
Dennis Plenker
Benjamin Solomon
Stefan A. Haas
Mirjam Koker
Denis Moro-Sibilot
Zoe Wainer
Janine Altmüller
Hélène Nagy-Mignotte
Yasushi Yatabe
Gavin M. Wright
Prudence A. Russell
Thomas Zander
Roopika Menon
Annamaria la Torre
Timothy Perera
Sandra Ortiz-Cuaran
Marc Parade
Marc Bos
Elisabeth Brambilla
Erich Stoelben
Ruping Sun
Christian Becker
Vito Michele Fazio
Martin Vingron
Roman K. Thomas
Wenzel Vogel
Jakob Schöttle
Peter Nürnberg
Sylvie Lantuejoul
Idoya Lahortiga
Iver Petersen
Hirotaka Osada
Jürgen Wolf
Roland T. Ullrich
Souichi Ogata
Lucia Anna Muscarella
Jörg Sänger
Lukas C. Heukamp
Joachim H. Clement
Christian Brambilla
Johannes M. Heuckmann
Lynnette Fernandez-Cuesta
Sascha Ansén
Sven Perner
Reinhard Buettner
Martin Peifer
Frauke Leenders
Juliane Daßler
Ilona Dahmen
Florian Malchers
Source :
Cancer Discovery; Vol 4, Cancer Discovery
Publication Year :
2014
Publisher :
AMER ASSOC CANCER RESEARCH, 2014.

Abstract

We discovered a novel somatic gene fusion, CD74–NRG1, by transcriptome sequencing of 25 lung adenocarcinomas of never smokers. By screening 102 lung adenocarcinomas negative for known oncogenic alterations, we found four additional fusion-positive tumors, all of which were of the invasive mucinous subtype. Mechanistically, CD74–NRG1 leads to extracellular expression of the EGF-like domain of NRG1 III-β3, thereby providing the ligand for ERBB2–ERBB3 receptor complexes. Accordingly, ERBB2 and ERBB3 expression was high in the index case, and expression of phospho-ERBB3 was specifically found in tumors bearing the fusion (P < 0.0001). Ectopic expression of CD74–NRG1 in lung cancer cell lines expressing ERBB2 and ERBB3 activated ERBB3 and the PI3K–AKT pathway, and led to increased colony formation in soft agar. Thus, CD74–NRG1 gene fusions are activating genomic alterations in invasive mucinous adenocarcinomas and may offer a therapeutic opportunity for a lung tumor subtype with, so far, no effective treatment. Significance: CD74–NRG1 fusions may represent a therapeutic opportunity for invasive mucinous lung adenocarcinomas, a tumor with no effective treatment that frequently presents with multifocal unresectable disease. Cancer Discov; 4(4); 415–22. ©2014 AACR. This article is highlighted in the In This Issue feature, p. 377

Details

Language :
English
ISSN :
21598274
Volume :
4
Issue :
4
Database :
OpenAIRE
Journal :
Cancer Discovery
Accession number :
edsair.doi.dedup.....46ff3f8cec3122a2965b6a2bf6f89a54
Full Text :
https://doi.org/10.1158/2159-8290.CD-13-0633