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Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma
BACKGROUND: Overexpression of heat shock protein 70 (HSP70) has been observed in many types of cancer including gastric adenocarcinomas, although the exact role of HSP70 in carcinogenesis remains unclear. METHODS: The study analyzed a total of 458 radical gastrectomy specimens which were immunohisto...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Pathologists and The Korean Society for Cytopathology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701817/ https://www.ncbi.nlm.nih.gov/pubmed/23837014 http://dx.doi.org/10.4132/KoreanJPathol.2013.47.3.219 |
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author | Kang, Youngran Jung, Woon Yong Lee, Hyunjoo Jung, Wonkyung Lee, Eunjung Shin, Bong Kyung Kim, Aeree Kim, Han Kyeom Kim, Baek-hui |
author_facet | Kang, Youngran Jung, Woon Yong Lee, Hyunjoo Jung, Wonkyung Lee, Eunjung Shin, Bong Kyung Kim, Aeree Kim, Han Kyeom Kim, Baek-hui |
author_sort | Kang, Youngran |
collection | PubMed |
description | BACKGROUND: Overexpression of heat shock protein 70 (HSP70) has been observed in many types of cancer including gastric adenocarcinomas, although the exact role of HSP70 in carcinogenesis remains unclear. METHODS: The study analyzed a total of 458 radical gastrectomy specimens which were immunohistochemically stained with HSP70, p53, and Ki-67 antibodies. RESULTS: The study determined that the expression of HSP70 was significantly increased in early gastric cancer (EGC) compared to advanced gastric cancer (p<0.001). The HSP70 expression was correlated with well-differentiated tumor type, intestinal type of Lauren classification and the lower pT and pN stage. Negative expression of Ki-67 and p53 expression was associated with poor prognosis. The study did not find any correlation between HSP70 and p53 expression. The study determined that HSP70 expression in the EGC subgroup was associated with a poor prognosis (p=0.009), as well as negative Ki-67 expression (p=0.006), but was not associated with p53. Based on multivariate analysis, HSP70 expression (p=0.024), negative expression of Ki-67, invasion depth and lymph node metastasis were determined to be independent prognostic markers. CONCLUSIONS: HSP70 is expressed in the early stages of gastric adenocarcinoma. In EGC, HSP70 is a poor independent prognostic marker and is correlated with a low proliferation index. |
format | Online Article Text |
id | pubmed-3701817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Korean Society of Pathologists and The Korean Society for Cytopathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-37018172013-07-08 Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma Kang, Youngran Jung, Woon Yong Lee, Hyunjoo Jung, Wonkyung Lee, Eunjung Shin, Bong Kyung Kim, Aeree Kim, Han Kyeom Kim, Baek-hui Korean J Pathol Original Article BACKGROUND: Overexpression of heat shock protein 70 (HSP70) has been observed in many types of cancer including gastric adenocarcinomas, although the exact role of HSP70 in carcinogenesis remains unclear. METHODS: The study analyzed a total of 458 radical gastrectomy specimens which were immunohistochemically stained with HSP70, p53, and Ki-67 antibodies. RESULTS: The study determined that the expression of HSP70 was significantly increased in early gastric cancer (EGC) compared to advanced gastric cancer (p<0.001). The HSP70 expression was correlated with well-differentiated tumor type, intestinal type of Lauren classification and the lower pT and pN stage. Negative expression of Ki-67 and p53 expression was associated with poor prognosis. The study did not find any correlation between HSP70 and p53 expression. The study determined that HSP70 expression in the EGC subgroup was associated with a poor prognosis (p=0.009), as well as negative Ki-67 expression (p=0.006), but was not associated with p53. Based on multivariate analysis, HSP70 expression (p=0.024), negative expression of Ki-67, invasion depth and lymph node metastasis were determined to be independent prognostic markers. CONCLUSIONS: HSP70 is expressed in the early stages of gastric adenocarcinoma. In EGC, HSP70 is a poor independent prognostic marker and is correlated with a low proliferation index. The Korean Society of Pathologists and The Korean Society for Cytopathology 2013-06 2013-06-25 /pmc/articles/PMC3701817/ /pubmed/23837014 http://dx.doi.org/10.4132/KoreanJPathol.2013.47.3.219 Text en © 2013 The Korean Society of Pathologists/The Korean Society for Cytopathology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kang, Youngran Jung, Woon Yong Lee, Hyunjoo Jung, Wonkyung Lee, Eunjung Shin, Bong Kyung Kim, Aeree Kim, Han Kyeom Kim, Baek-hui Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma |
title | Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma |
title_full | Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma |
title_fullStr | Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma |
title_full_unstemmed | Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma |
title_short | Prognostic Significance of Heat Shock Protein 70 Expression in Early Gastric Carcinoma |
title_sort | prognostic significance of heat shock protein 70 expression in early gastric carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701817/ https://www.ncbi.nlm.nih.gov/pubmed/23837014 http://dx.doi.org/10.4132/KoreanJPathol.2013.47.3.219 |
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