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Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer

Purpose: This study aimed to investigate the relationship between DNA damage response (DDR) related protein expression and clinical outcomes of patients with stage II and III gastric cancer undergoing gastrectomy. Materials and Methods: From January 2005 to December 2017, 217 gastrectomized patients...

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Autores principales: Park, Song Ee, Kim, Hee Sung, Jung, Eun-Jung, Suh, Ja Hee, Min, Hyeyoung, Chi, Kyong-Choun, Kim, Jong Won, Park, Joong-Min, Hwang, In Gyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824884/
https://www.ncbi.nlm.nih.gov/pubmed/35154455
http://dx.doi.org/10.7150/jca.65145
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author Park, Song Ee
Kim, Hee Sung
Jung, Eun-Jung
Suh, Ja Hee
Min, Hyeyoung
Chi, Kyong-Choun
Kim, Jong Won
Park, Joong-Min
Hwang, In Gyu
author_facet Park, Song Ee
Kim, Hee Sung
Jung, Eun-Jung
Suh, Ja Hee
Min, Hyeyoung
Chi, Kyong-Choun
Kim, Jong Won
Park, Joong-Min
Hwang, In Gyu
author_sort Park, Song Ee
collection PubMed
description Purpose: This study aimed to investigate the relationship between DNA damage response (DDR) related protein expression and clinical outcomes of patients with stage II and III gastric cancer undergoing gastrectomy. Materials and Methods: From January 2005 to December 2017, 217 gastrectomized patients with stage II and III gastric cancer were analyzed for disease-free and overall survival (DFS and OS, respectively) based on their DDR expression status. We performed the immunohistochemical assessment of MLH1, MSH2, at-rich interaction domain 1 (ARID1A), poly adenosine diphosphate-ribose polymerase 1 (PARP-1), breast cancer susceptibility gene 1 (BRCA1), and ataxia-telangiectasia mutated (ATM) using formalin-fixed paraffin-embedded (FFPE) samples. Results: Among the 217 patients studied, the most common DDR gene whose expression was suppressed was high PARP-1 (n = 120, 55.3%), followed by ATM (n = 62, 28.6%), ARID1A (n = 45, 20.7%), MLH1 (n = 33, 15.2%), BRCA1 (n = 25, 11.5%), and MSH2 (n = 9, 4.1%). The low-expression PARP-1 group exhibited a significantly shorter 5-year OS rate than the high-expression PARP-1 group (48.1% vs. 62.7%; HR 1.519, 95% CI = 1.011-2.283, P = 0.044). In the multivariate OS analysis, TNM stage (II vs. III) (HR = 5.172, P < 0.001), low PARP-1 expression (HR = 1.697, P = 0.013) and adjuvant chemotherapy (HR = 0.382, P < 0.001) were the only significant prognostic factors. Conclusions: Low PARP-1 expression level could be an indicator of poor prognosis in gastrectomized patients with stage II and III gastric cancer.
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spelling pubmed-88248842022-02-11 Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer Park, Song Ee Kim, Hee Sung Jung, Eun-Jung Suh, Ja Hee Min, Hyeyoung Chi, Kyong-Choun Kim, Jong Won Park, Joong-Min Hwang, In Gyu J Cancer Research Paper Purpose: This study aimed to investigate the relationship between DNA damage response (DDR) related protein expression and clinical outcomes of patients with stage II and III gastric cancer undergoing gastrectomy. Materials and Methods: From January 2005 to December 2017, 217 gastrectomized patients with stage II and III gastric cancer were analyzed for disease-free and overall survival (DFS and OS, respectively) based on their DDR expression status. We performed the immunohistochemical assessment of MLH1, MSH2, at-rich interaction domain 1 (ARID1A), poly adenosine diphosphate-ribose polymerase 1 (PARP-1), breast cancer susceptibility gene 1 (BRCA1), and ataxia-telangiectasia mutated (ATM) using formalin-fixed paraffin-embedded (FFPE) samples. Results: Among the 217 patients studied, the most common DDR gene whose expression was suppressed was high PARP-1 (n = 120, 55.3%), followed by ATM (n = 62, 28.6%), ARID1A (n = 45, 20.7%), MLH1 (n = 33, 15.2%), BRCA1 (n = 25, 11.5%), and MSH2 (n = 9, 4.1%). The low-expression PARP-1 group exhibited a significantly shorter 5-year OS rate than the high-expression PARP-1 group (48.1% vs. 62.7%; HR 1.519, 95% CI = 1.011-2.283, P = 0.044). In the multivariate OS analysis, TNM stage (II vs. III) (HR = 5.172, P < 0.001), low PARP-1 expression (HR = 1.697, P = 0.013) and adjuvant chemotherapy (HR = 0.382, P < 0.001) were the only significant prognostic factors. Conclusions: Low PARP-1 expression level could be an indicator of poor prognosis in gastrectomized patients with stage II and III gastric cancer. Ivyspring International Publisher 2022-01-01 /pmc/articles/PMC8824884/ /pubmed/35154455 http://dx.doi.org/10.7150/jca.65145 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Park, Song Ee
Kim, Hee Sung
Jung, Eun-Jung
Suh, Ja Hee
Min, Hyeyoung
Chi, Kyong-Choun
Kim, Jong Won
Park, Joong-Min
Hwang, In Gyu
Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer
title Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer
title_full Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer
title_fullStr Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer
title_full_unstemmed Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer
title_short Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer
title_sort low parp-1 expression level is an indicator of poor prognosis in patients with stage ii and iii gastric cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824884/
https://www.ncbi.nlm.nih.gov/pubmed/35154455
http://dx.doi.org/10.7150/jca.65145
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