Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review

Abstract Background Esophageal squamous cell carcinoma (ESCC) is an aggressive malignancy, with a high incidence and poor prognosis. In the past several decades, hundreds of proteins have been reported to be associated with the prognosis of ESCC, but none has been widely accepted to guide clinical c...

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Main Authors: Chunni Wang, Jingnan Wang, Zhaoli Chen, Yibo Gao, Jie He
Format: Article
Language:English
Published: BMC 2017-08-01
Series:Chinese Journal of Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40880-017-0232-5
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spelling doaj-463007a916154c79bbdacac6caa103582020-11-24T22:21:04ZengBMCChinese Journal of Cancer1944-446X2017-08-0136111710.1186/s40880-017-0232-5Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic reviewChunni Wang0Jingnan Wang1Zhaoli Chen2Yibo Gao3Jie He4Department of Thoracic Surgery, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Thoracic Surgery, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Thoracic Surgery, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Thoracic Surgery, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Thoracic Surgery, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeAbstract Background Esophageal squamous cell carcinoma (ESCC) is an aggressive malignancy, with a high incidence and poor prognosis. In the past several decades, hundreds of proteins have been reported to be associated with the prognosis of ESCC, but none has been widely accepted to guide clinical care. This study aimed to identify proteins with great potential for predicting prognosis of ESCC. Methods We conducted a systematic review on immunohistochemical (IHC) prognostic markers of ESCC according to the 2009 Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Guidelines. Literature related to IHC prognostic markers of ESCC were searched from PubMed, Embase, Web of Science, and Cochrane Library until January 30th, 2017. The risk of bias of these original studies was evaluated using the Quality in Prognosis Studies (QUIPS) tool. Results We identified 11 emerging IHC markers with reproducible results, including eight markers [epidermal growth factor receptor (EGFR), Cyclin D1, vascular endothelial growth factor (VEGF), Survivin, Podoplanin, Fascin, phosphorylated mammalian target of rapamycin (p-mTOR), and pyruvate kinase M2 (PKM2)] indicating unfavorable prognosis and 3 markers (P27, P16, and E-cadherin) indicating favorable prognosis of ESCC. Conclusion Strong evidence supports that these 11 emerging IHC markers or their combinations may be useful in predicting prognosis and aiding personalized therapy decision-making for ESCC patients.http://link.springer.com/article/10.1186/s40880-017-0232-5Esophageal squamous cell carcinomaPrognosisSurvivalImmunohistochemical markers
collection DOAJ
language English
format Article
sources DOAJ
author Chunni Wang
Jingnan Wang
Zhaoli Chen
Yibo Gao
Jie He
spellingShingle Chunni Wang
Jingnan Wang
Zhaoli Chen
Yibo Gao
Jie He
Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
Chinese Journal of Cancer
Esophageal squamous cell carcinoma
Prognosis
Survival
Immunohistochemical markers
author_facet Chunni Wang
Jingnan Wang
Zhaoli Chen
Yibo Gao
Jie He
author_sort Chunni Wang
title Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
title_short Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
title_full Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
title_fullStr Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
title_full_unstemmed Immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
title_sort immunohistochemical prognostic markers of esophageal squamous cell carcinoma: a systematic review
publisher BMC
series Chinese Journal of Cancer
issn 1944-446X
publishDate 2017-08-01
description Abstract Background Esophageal squamous cell carcinoma (ESCC) is an aggressive malignancy, with a high incidence and poor prognosis. In the past several decades, hundreds of proteins have been reported to be associated with the prognosis of ESCC, but none has been widely accepted to guide clinical care. This study aimed to identify proteins with great potential for predicting prognosis of ESCC. Methods We conducted a systematic review on immunohistochemical (IHC) prognostic markers of ESCC according to the 2009 Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Guidelines. Literature related to IHC prognostic markers of ESCC were searched from PubMed, Embase, Web of Science, and Cochrane Library until January 30th, 2017. The risk of bias of these original studies was evaluated using the Quality in Prognosis Studies (QUIPS) tool. Results We identified 11 emerging IHC markers with reproducible results, including eight markers [epidermal growth factor receptor (EGFR), Cyclin D1, vascular endothelial growth factor (VEGF), Survivin, Podoplanin, Fascin, phosphorylated mammalian target of rapamycin (p-mTOR), and pyruvate kinase M2 (PKM2)] indicating unfavorable prognosis and 3 markers (P27, P16, and E-cadherin) indicating favorable prognosis of ESCC. Conclusion Strong evidence supports that these 11 emerging IHC markers or their combinations may be useful in predicting prognosis and aiding personalized therapy decision-making for ESCC patients.
topic Esophageal squamous cell carcinoma
Prognosis
Survival
Immunohistochemical markers
url http://link.springer.com/article/10.1186/s40880-017-0232-5
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