P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers

<p>Abstract</p> <p>Members of Shc (src homology and collagen homology) family, p46shc, p52shc, p66shc have known to be related to cell proliferation and carcinogenesis. Whereas p46shc and p52shc drive the reaction forward, the role of p66shc in cancers remains to be understood clea...

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Main Authors: Wani Nisar A, Naqash Sameer, Hamza Rouf, Baba Rafia A, Bhat Hina F, Kirmani Deeba, Bashir Muneesa, Andrabi Khurshid I, Zargar Mohammad A, Khanday Firdous A
Format: Article
Language:English
Published: BMC 2010-06-01
Series:Cell Communication and Signaling
Online Access:http://www.biosignaling.com/content/8/1/13
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author Wani Nisar A
Naqash Sameer
Hamza Rouf
Baba Rafia A
Bhat Hina F
Kirmani Deeba
Bashir Muneesa
Andrabi Khurshid I
Zargar Mohammad A
Khanday Firdous A
author_facet Wani Nisar A
Naqash Sameer
Hamza Rouf
Baba Rafia A
Bhat Hina F
Kirmani Deeba
Bashir Muneesa
Andrabi Khurshid I
Zargar Mohammad A
Khanday Firdous A
author_sort Wani Nisar A
collection DOAJ
description <p>Abstract</p> <p>Members of Shc (src homology and collagen homology) family, p46shc, p52shc, p66shc have known to be related to cell proliferation and carcinogenesis. Whereas p46shc and p52shc drive the reaction forward, the role of p66shc in cancers remains to be understood clearly. Hence, their expression in cancers needs to be evaluated carefully so that Shc analysis may provide prognostic information in the development of carcinogenesis. In the present study, the expression of p66shc and its associate targets namely Eps8 (epidermal pathway substrate 8), Rac1 (ras-related C3 botulinum toxin substrate1) and Grb2 (growth factor receptor bound protein 2) were examined in fresh tissue specimens from patients with esophageal squamous cell carcinoma and esophageal adenocarcinoma using western blot analysis. A thorough analysis of both esophageal squamous cell carcinoma and adenocarcinoma showed p66shc expression to be significantly higher in both types of carcinomas as compared to the controls. The controls of adenocarcinoma show a higher basal expression level of p66shc as compared to the controls of squamous cell carcinoma. The expression level of downstream targets of p66shc i.e., eps8 and rac1 was also found to be consistently higher in human esophageal carcinomas, and hence correlated positively with p66shc expression. However the expression of grb2 was found to be equal in both esophageal squamous cell carcinoma and adenocarcinoma. The above results suggest that the pathway operated by p66shc in cancers does not involve the participation of Ras and Grb2 as downstream targets instead it operates the pathway involving Eps8 and Rac1 proteins. From the results it is also suggestive that p66shc may have a role in the regulation of esophageal carcinomas and represents a possible mechanism of signaling for the development of squamous cell carcinoma and adenocarcinoma of esophagus.</p>
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spelling doaj.art-dadfff0190974160ac7a47ba2190773e2022-12-22T01:07:54ZengBMCCell Communication and Signaling1478-811X2010-06-01811310.1186/1478-811X-8-13P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancersWani Nisar ANaqash SameerHamza RoufBaba Rafia ABhat Hina FKirmani DeebaBashir MuneesaAndrabi Khurshid IZargar Mohammad AKhanday Firdous A<p>Abstract</p> <p>Members of Shc (src homology and collagen homology) family, p46shc, p52shc, p66shc have known to be related to cell proliferation and carcinogenesis. Whereas p46shc and p52shc drive the reaction forward, the role of p66shc in cancers remains to be understood clearly. Hence, their expression in cancers needs to be evaluated carefully so that Shc analysis may provide prognostic information in the development of carcinogenesis. In the present study, the expression of p66shc and its associate targets namely Eps8 (epidermal pathway substrate 8), Rac1 (ras-related C3 botulinum toxin substrate1) and Grb2 (growth factor receptor bound protein 2) were examined in fresh tissue specimens from patients with esophageal squamous cell carcinoma and esophageal adenocarcinoma using western blot analysis. A thorough analysis of both esophageal squamous cell carcinoma and adenocarcinoma showed p66shc expression to be significantly higher in both types of carcinomas as compared to the controls. The controls of adenocarcinoma show a higher basal expression level of p66shc as compared to the controls of squamous cell carcinoma. The expression level of downstream targets of p66shc i.e., eps8 and rac1 was also found to be consistently higher in human esophageal carcinomas, and hence correlated positively with p66shc expression. However the expression of grb2 was found to be equal in both esophageal squamous cell carcinoma and adenocarcinoma. The above results suggest that the pathway operated by p66shc in cancers does not involve the participation of Ras and Grb2 as downstream targets instead it operates the pathway involving Eps8 and Rac1 proteins. From the results it is also suggestive that p66shc may have a role in the regulation of esophageal carcinomas and represents a possible mechanism of signaling for the development of squamous cell carcinoma and adenocarcinoma of esophagus.</p>http://www.biosignaling.com/content/8/1/13
spellingShingle Wani Nisar A
Naqash Sameer
Hamza Rouf
Baba Rafia A
Bhat Hina F
Kirmani Deeba
Bashir Muneesa
Andrabi Khurshid I
Zargar Mohammad A
Khanday Firdous A
P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers
Cell Communication and Signaling
title P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers
title_full P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers
title_fullStr P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers
title_full_unstemmed P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers
title_short P66shc and its downstream Eps8 and Rac1 proteins are upregulated in esophageal cancers
title_sort p66shc and its downstream eps8 and rac1 proteins are upregulated in esophageal cancers
url http://www.biosignaling.com/content/8/1/13
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