Calpain system protein expression in carcinomas of the pancreas, bile duct and ampulla
Background: Pancreatic cancer, including cancer of the ampulla of Vater and bile duct, is very aggressive and has a poor five year survival rate; improved methods of patient stratification are required. Methods: We assessed the expression of calpain-1, calpain-2 and calpastatin in two patient coho...
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| Format: | Article |
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BioMed Central
2012
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| Online Access: | https://eprints.nottingham.ac.uk/2784/ |
| _version_ | 1848790874478084096 |
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| author | Storr, Sarah J. Zaitoun, Abed M. Arora, Arvind Durrant, Lindy G. Lobo, Dileep N. Madhusudan, Srinivasan Martin, Stewart G. |
| author_facet | Storr, Sarah J. Zaitoun, Abed M. Arora, Arvind Durrant, Lindy G. Lobo, Dileep N. Madhusudan, Srinivasan Martin, Stewart G. |
| author_sort | Storr, Sarah J. |
| building | Nottingham Research Data Repository |
| collection | Online Access |
| description | Background: Pancreatic cancer, including cancer of the ampulla of Vater and bile duct, is very aggressive and has a
poor five year survival rate; improved methods of patient stratification are required.
Methods: We assessed the expression of calpain-1, calpain-2 and calpastatin in two patient cohorts using
immunohistochemistry on tissue microarrays. The first cohort was composed of 68 pancreatic adenocarcinomas
and the second cohort was composed of 120 cancers of the bile duct and ampulla.
Results: In bile duct and ampullary carcinomas an association was observed between cytoplasmic calpastatin
expression and patient age (P = 0.036), and between nuclear calpastatin expression and increased tumour stage
(P = 0.026) and the presence of vascular invasion (P = 0.043). In pancreatic cancer, high calpain-2 expression was
significantly associated with improved overall survival (P = 0.036), which remained significant in multivariate
Cox-regression analysis (hazard ratio = 0.342; 95% confidence interva l = 0.157-0.741; P = 0.007). In cancers of the
bile duct and ampulla, low cytoplasmic expression of calpastatin was significantly associated with poor overall
survival (P = 0.012), which remained significant in multivariate Cox-regression analysis (hazard ratio = 0.595; 95%
confidence interval = 0.365-0.968; P = 0.037).
Conclusion: The results suggest that calpain-2 and calpastatin expression is important in pancreatic cancers,
influencing disease progression. The findings of this study warrant a larger follow-up study.
Keywords: Calpain, Calpastatin, Pancreas, Ampulla, Bile duct, Cancer |
| first_indexed | 2025-11-14T18:19:33Z |
| format | Article |
| id | nottingham-2784 |
| institution | University of Nottingham Malaysia Campus |
| institution_category | Local University |
| last_indexed | 2025-11-14T18:19:33Z |
| publishDate | 2012 |
| publisher | BioMed Central |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | nottingham-27842020-05-04T16:34:48Z https://eprints.nottingham.ac.uk/2784/ Calpain system protein expression in carcinomas of the pancreas, bile duct and ampulla Storr, Sarah J. Zaitoun, Abed M. Arora, Arvind Durrant, Lindy G. Lobo, Dileep N. Madhusudan, Srinivasan Martin, Stewart G. Background: Pancreatic cancer, including cancer of the ampulla of Vater and bile duct, is very aggressive and has a poor five year survival rate; improved methods of patient stratification are required. Methods: We assessed the expression of calpain-1, calpain-2 and calpastatin in two patient cohorts using immunohistochemistry on tissue microarrays. The first cohort was composed of 68 pancreatic adenocarcinomas and the second cohort was composed of 120 cancers of the bile duct and ampulla. Results: In bile duct and ampullary carcinomas an association was observed between cytoplasmic calpastatin expression and patient age (P = 0.036), and between nuclear calpastatin expression and increased tumour stage (P = 0.026) and the presence of vascular invasion (P = 0.043). In pancreatic cancer, high calpain-2 expression was significantly associated with improved overall survival (P = 0.036), which remained significant in multivariate Cox-regression analysis (hazard ratio = 0.342; 95% confidence interva l = 0.157-0.741; P = 0.007). In cancers of the bile duct and ampulla, low cytoplasmic expression of calpastatin was significantly associated with poor overall survival (P = 0.012), which remained significant in multivariate Cox-regression analysis (hazard ratio = 0.595; 95% confidence interval = 0.365-0.968; P = 0.037). Conclusion: The results suggest that calpain-2 and calpastatin expression is important in pancreatic cancers, influencing disease progression. The findings of this study warrant a larger follow-up study. Keywords: Calpain, Calpastatin, Pancreas, Ampulla, Bile duct, Cancer BioMed Central 2012-11-09 Article PeerReviewed Storr, Sarah J., Zaitoun, Abed M., Arora, Arvind, Durrant, Lindy G., Lobo, Dileep N., Madhusudan, Srinivasan and Martin, Stewart G. (2012) Calpain system protein expression in carcinomas of the pancreas, bile duct and ampulla. BMC Cancer, 12 (511). ISSN 1471-2407 http://www.biomedcentral.com/1471-2407/12/511/ doi:10.1186/1471-2407-12-511 doi:10.1186/1471-2407-12-511 |
| spellingShingle | Storr, Sarah J. Zaitoun, Abed M. Arora, Arvind Durrant, Lindy G. Lobo, Dileep N. Madhusudan, Srinivasan Martin, Stewart G. Calpain system protein expression in carcinomas of the pancreas, bile duct and ampulla |
| title | Calpain system protein expression in carcinomas of the
pancreas, bile duct and ampulla |
| title_full | Calpain system protein expression in carcinomas of the
pancreas, bile duct and ampulla |
| title_fullStr | Calpain system protein expression in carcinomas of the
pancreas, bile duct and ampulla |
| title_full_unstemmed | Calpain system protein expression in carcinomas of the
pancreas, bile duct and ampulla |
| title_short | Calpain system protein expression in carcinomas of the
pancreas, bile duct and ampulla |
| title_sort | calpain system protein expression in carcinomas of the
pancreas, bile duct and ampulla |
| url | https://eprints.nottingham.ac.uk/2784/ https://eprints.nottingham.ac.uk/2784/ https://eprints.nottingham.ac.uk/2784/ |