Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer.
Gastric carcinoma is one of the major causes of cancer-related mortality worldwide. Early detection and treatment leads to an excellent prognosis in patients with early gastric cancer (EGC), whereas the prognosis of patients with advanced gastric cancer (AGC) remains poor. It is unclear whether EGCs...
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doaj-93d1d4031b09448d89bd271c191d75cd2020-11-25T01:13:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8277010.1371/journal.pone.0082770Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer.Guhyun KangWoo Cheol HwangIn-Gu DoKai WangSo Young KangJeeyun LeeSe Hoon ParkJoon Oh ParkWon Ki KangJiryeon JangMin-Gew ChoiJun Ho LeeTae Sung SohnJae Moon BaeSung KimMin Ji KimSeonwoo KimCheol Keun ParkKyoung-Mee KimGastric carcinoma is one of the major causes of cancer-related mortality worldwide. Early detection and treatment leads to an excellent prognosis in patients with early gastric cancer (EGC), whereas the prognosis of patients with advanced gastric cancer (AGC) remains poor. It is unclear whether EGCs and AGCs are distinct entities or whether EGCs are the beginning stages of AGCs. We performed whole exome sequencing of four samples from patients with EGC and compared the results with those from AGCs. In both EGCs and AGCs, a total of 268 genes were commonly mutated and independent mutations were additionally found in EGCs (516 genes) and AGCs (3104 genes). A higher frequency of C>G transitions was observed in intestinal-type compared to diffuse-type carcinomas (P = 0.010). The DYRK3, GPR116, MCM10, PCDH17, PCDHB1, RDH5 and UNC5C genes are recurrently mutated in EGCs and may be involved in early carcinogenesis.http://europepmc.org/articles/PMC3871845?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Guhyun Kang Woo Cheol Hwang In-Gu Do Kai Wang So Young Kang Jeeyun Lee Se Hoon Park Joon Oh Park Won Ki Kang Jiryeon Jang Min-Gew Choi Jun Ho Lee Tae Sung Sohn Jae Moon Bae Sung Kim Min Ji Kim Seonwoo Kim Cheol Keun Park Kyoung-Mee Kim |
spellingShingle |
Guhyun Kang Woo Cheol Hwang In-Gu Do Kai Wang So Young Kang Jeeyun Lee Se Hoon Park Joon Oh Park Won Ki Kang Jiryeon Jang Min-Gew Choi Jun Ho Lee Tae Sung Sohn Jae Moon Bae Sung Kim Min Ji Kim Seonwoo Kim Cheol Keun Park Kyoung-Mee Kim Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. PLoS ONE |
author_facet |
Guhyun Kang Woo Cheol Hwang In-Gu Do Kai Wang So Young Kang Jeeyun Lee Se Hoon Park Joon Oh Park Won Ki Kang Jiryeon Jang Min-Gew Choi Jun Ho Lee Tae Sung Sohn Jae Moon Bae Sung Kim Min Ji Kim Seonwoo Kim Cheol Keun Park Kyoung-Mee Kim |
author_sort |
Guhyun Kang |
title |
Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. |
title_short |
Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. |
title_full |
Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. |
title_fullStr |
Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. |
title_full_unstemmed |
Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. |
title_sort |
exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
Gastric carcinoma is one of the major causes of cancer-related mortality worldwide. Early detection and treatment leads to an excellent prognosis in patients with early gastric cancer (EGC), whereas the prognosis of patients with advanced gastric cancer (AGC) remains poor. It is unclear whether EGCs and AGCs are distinct entities or whether EGCs are the beginning stages of AGCs. We performed whole exome sequencing of four samples from patients with EGC and compared the results with those from AGCs. In both EGCs and AGCs, a total of 268 genes were commonly mutated and independent mutations were additionally found in EGCs (516 genes) and AGCs (3104 genes). A higher frequency of C>G transitions was observed in intestinal-type compared to diffuse-type carcinomas (P = 0.010). The DYRK3, GPR116, MCM10, PCDH17, PCDHB1, RDH5 and UNC5C genes are recurrently mutated in EGCs and may be involved in early carcinogenesis. |
url |
http://europepmc.org/articles/PMC3871845?pdf=render |
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