Germline mutations causing familial lung cancer View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2015-07-16

AUTHORS

Koichi Tomoshige, Keitaro Matsumoto, Tomoshi Tsuchiya, Masahiro Oikawa, Takuro Miyazaki, Naoya Yamasaki, Hiroyuki Mishima, Akira Kinoshita, Toru Kubo, Kiyoyasu Fukushima, Koh-ichiro Yoshiura, Takeshi Nagayasu

ABSTRACT

Genetic factors are important in lung cancer, but as most lung cancers are sporadic, little is known about inherited genetic factors. We identified a three-generation family with suspected autosomal dominant inherited lung cancer susceptibility. Sixteen individuals in the family had lung cancer. To identify the gene(s) that cause lung cancer in this pedigree, we extracted DNA from the peripheral blood of three individuals and from the blood of one cancer-free control family member and performed whole-exome sequencing. We identified 41 alterations in 40 genes in all affected family members but not in the unaffected member. These were considered candidate mutations for familial lung cancer. Next, to identify somatic mutations and/or inherited alterations in these 40 genes among sporadic lung cancers, we performed exon target enrichment sequencing using 192 samples from sporadic lung cancer patients. We detected somatic ‘candidate’ mutations in multiple sporadic lung cancer samples; MAST1, CENPE, CACNB2 and LCT were the most promising candidate genes. In addition, the MAST1 gene was located in a putative cancer-linked locus in the pedigree. Our data suggest that several genes act as oncogenic drivers in this family, and that MAST1 is most likely to cause lung cancer. More... »

PAGES

597-603

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/jhg.2015.75

DOI

http://dx.doi.org/10.1038/jhg.2015.75

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1012938525

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/26178433


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