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Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis

SNP rs2294008 in Prostate Stem Cell Antigen (PSCA) and decreased PSCA expression are associated with gastric cancer. The objective of this study is to investigate the role of rs2294008 and PSCA expression in the gastritis-gastric cancer carcinogenic pathway. We conducted a case-control association s...

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Autores principales: Toyoshima, Osamu, Tanikawa, Chizu, Yamamoto, Ryuta, Watanabe, Hidenobu, Yamashita, Hiroharu, Sakitani, Kosuke, Yoshida, Shuntaro, Kubo, Michiaki, Matsuo, Keitaro, Ito, Hidemi, Koike, Kazuhiko, Seto, Yasuyuki, Matsuda, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790512/
https://www.ncbi.nlm.nih.gov/pubmed/29423095
http://dx.doi.org/10.18632/oncotarget.23278
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author Toyoshima, Osamu
Tanikawa, Chizu
Yamamoto, Ryuta
Watanabe, Hidenobu
Yamashita, Hiroharu
Sakitani, Kosuke
Yoshida, Shuntaro
Kubo, Michiaki
Matsuo, Keitaro
Ito, Hidemi
Koike, Kazuhiko
Seto, Yasuyuki
Matsuda, Koichi
author_facet Toyoshima, Osamu
Tanikawa, Chizu
Yamamoto, Ryuta
Watanabe, Hidenobu
Yamashita, Hiroharu
Sakitani, Kosuke
Yoshida, Shuntaro
Kubo, Michiaki
Matsuo, Keitaro
Ito, Hidemi
Koike, Kazuhiko
Seto, Yasuyuki
Matsuda, Koichi
author_sort Toyoshima, Osamu
collection PubMed
description SNP rs2294008 in Prostate Stem Cell Antigen (PSCA) and decreased PSCA expression are associated with gastric cancer. The objective of this study is to investigate the role of rs2294008 and PSCA expression in the gastritis-gastric cancer carcinogenic pathway. We conducted a case-control association study of H. pylori-infected gastritis and gastric cancer. rs2294008 was associated with the progression to chronic active gastritis (P = 9.4 × 10(–5); odds ratio = 3.88, TT + TC vs CC genotype), but not with H. pylori infection per se nor with the progression from active gastritis to gastric cancer. We also assessed the association of rs2294008 with PSCA mRNA expression in the gastric mucosa at various disease stages and found that rs2294008 was associated with PSCA expression (P = 1.3 × 10(–12)). H. pylori infection (P = 5.1 × 10(–8)) and eradication therapy (P < 1 × 10(–11)) resulted in the reduced and increased PSCA expression, respectively, indicating negative regulation of PSCA expression by H. pylori infection. PSCA expression was decreased in severe gastritis compared with mild gastritis only among T allele carriers. Our findings revealed the regulation of PSCA expression by host genetic variation and bacterial infection might contribute to gastritis progression after H. pylori infection.
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spelling pubmed-57905122018-02-08 Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis Toyoshima, Osamu Tanikawa, Chizu Yamamoto, Ryuta Watanabe, Hidenobu Yamashita, Hiroharu Sakitani, Kosuke Yoshida, Shuntaro Kubo, Michiaki Matsuo, Keitaro Ito, Hidemi Koike, Kazuhiko Seto, Yasuyuki Matsuda, Koichi Oncotarget Research Paper SNP rs2294008 in Prostate Stem Cell Antigen (PSCA) and decreased PSCA expression are associated with gastric cancer. The objective of this study is to investigate the role of rs2294008 and PSCA expression in the gastritis-gastric cancer carcinogenic pathway. We conducted a case-control association study of H. pylori-infected gastritis and gastric cancer. rs2294008 was associated with the progression to chronic active gastritis (P = 9.4 × 10(–5); odds ratio = 3.88, TT + TC vs CC genotype), but not with H. pylori infection per se nor with the progression from active gastritis to gastric cancer. We also assessed the association of rs2294008 with PSCA mRNA expression in the gastric mucosa at various disease stages and found that rs2294008 was associated with PSCA expression (P = 1.3 × 10(–12)). H. pylori infection (P = 5.1 × 10(–8)) and eradication therapy (P < 1 × 10(–11)) resulted in the reduced and increased PSCA expression, respectively, indicating negative regulation of PSCA expression by H. pylori infection. PSCA expression was decreased in severe gastritis compared with mild gastritis only among T allele carriers. Our findings revealed the regulation of PSCA expression by host genetic variation and bacterial infection might contribute to gastritis progression after H. pylori infection. Impact Journals LLC 2017-12-14 /pmc/articles/PMC5790512/ /pubmed/29423095 http://dx.doi.org/10.18632/oncotarget.23278 Text en Copyright: © 2018 Toyoshima et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Toyoshima, Osamu
Tanikawa, Chizu
Yamamoto, Ryuta
Watanabe, Hidenobu
Yamashita, Hiroharu
Sakitani, Kosuke
Yoshida, Shuntaro
Kubo, Michiaki
Matsuo, Keitaro
Ito, Hidemi
Koike, Kazuhiko
Seto, Yasuyuki
Matsuda, Koichi
Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis
title Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis
title_full Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis
title_fullStr Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis
title_full_unstemmed Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis
title_short Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis
title_sort decrease in psca expression caused by helicobacter pylori infection may promote progression to severe gastritis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790512/
https://www.ncbi.nlm.nih.gov/pubmed/29423095
http://dx.doi.org/10.18632/oncotarget.23278
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