TY - JOUR
T1 - Widespread somatic L1 retrotransposition occurs early during gastrointestinal cancer evolution
AU - Ewing, Adam D
AU - Gacita, Anthony
AU - Wood, Laura D
AU - Ma, Florence
AU - Xing, Dongmei
AU - Kim, Min-Sik
AU - Manda, Srikanth S
AU - Abril, Gabriela
AU - Pereira, Gavin
AU - Makohon-Moore, Alvin
AU - Looijenga, Leendert H J
AU - Gillis, Ad J M
AU - Hruban, Ralph H
AU - Anders, Robert A
AU - Romans, Katharine E
AU - Pandey, Akhilesh
AU - Iacobuzio-Donahue, Christine A
AU - Vogelstein, Bert
AU - Kinzler, Kenneth W
AU - Kazazian, Haig H
AU - Solyom, Szilvia
N1 - © 2015 Ewing et al.; Published by Cold Spring Harbor Laboratory Press.
PY - 2015/10
Y1 - 2015/10
N2 - Somatic L1 retrotransposition events have been shown to occur in epithelial cancers. Here, we attempted to determine how early somatic L1 insertions occurred during the development of gastrointestinal (GI) cancers. Using L1-targeted resequencing (L1-seq), we studied different stages of four colorectal cancers arising from colonic polyps, seven pancreatic carcinomas, as well as seven gastric cancers. Surprisingly, we found somatic L1 insertions not only in all cancer types and metastases but also in colonic adenomas, well-known cancer precursors. Some insertions were also present in low quantities in normal GI tissues, occasionally caught in the act of being clonally fixed in the adjacent tumors. Insertions in adenomas and cancers numbered in the hundreds, and many were present in multiple tumor sections, implying clonal distribution. Our results demonstrate that extensive somatic insertional mutagenesis occurs very early during the development of GI tumors, probably before dysplastic growth.
AB - Somatic L1 retrotransposition events have been shown to occur in epithelial cancers. Here, we attempted to determine how early somatic L1 insertions occurred during the development of gastrointestinal (GI) cancers. Using L1-targeted resequencing (L1-seq), we studied different stages of four colorectal cancers arising from colonic polyps, seven pancreatic carcinomas, as well as seven gastric cancers. Surprisingly, we found somatic L1 insertions not only in all cancer types and metastases but also in colonic adenomas, well-known cancer precursors. Some insertions were also present in low quantities in normal GI tissues, occasionally caught in the act of being clonally fixed in the adjacent tumors. Insertions in adenomas and cancers numbered in the hundreds, and many were present in multiple tumor sections, implying clonal distribution. Our results demonstrate that extensive somatic insertional mutagenesis occurs very early during the development of GI tumors, probably before dysplastic growth.
KW - Disease Progression
KW - Gastrointestinal Neoplasms/genetics
KW - Gene Expression Profiling
KW - Gene Expression Regulation, Neoplastic
KW - Humans
KW - Long Interspersed Nucleotide Elements
KW - Mutagenesis, Insertional
KW - Neoplasm Proteins/biosynthesis
KW - Oligonucleotide Array Sequence Analysis
KW - Time Factors
UR - http://www.scopus.com/inward/record.url?scp=84941923663&partnerID=8YFLogxK
U2 - 10.1101/gr.196238.115
DO - 10.1101/gr.196238.115
M3 - Article
C2 - 26260970
SN - 1088-9051
VL - 25
SP - 1536
EP - 1545
JO - Genome research
JF - Genome research
IS - 10
ER -