Cathepsin E expression and activity: Role in the detection and treatment of pancreatic cancer

Corbin Pontious, Sabrina Kaul, Marcus Hong, Phil A. Hart, Somashekar G. Krishna, Luis F. Lara, Darwin L. Conwell, Zobeida Cruz-Monserrate

Producción científica: Review articlerevisión exhaustiva

42 Citas (Scopus)

Resumen

Cathepsin E (CTSE) is an intracellular, hydrolytic aspartic protease found to be expressed in cells of the immune and gastrointestinal systems, lymphoid tissues, erythrocytes, and cancer cells. The precise functions are not fully understood; however, various studies have investigated its numerous cell-type specific roles. CTSE expression has been shown to be a potential early biomarker for pancreatic ductal adenocarcinoma (PDAC). PDAC patients have low survival rates mostly due to the lack of early detection methods. CTSE-specific activity probes have been developed and tested to assist in tumor imaging and functional studies investigating the role of CTSE expression in PDAC tumors. Furthermore, a CTSE protease-specific, photodynamic therapy pro-drug was developed to explore its potential use to treat tumors that express CTSE. Since CTSE is expressed in pancreatic diseases that are risk factors for PDAC, such as pancreatic cysts and chronic pancreatitis, learning about its function in these disease types could assist in early PDAC detection and in understanding the biology of PDAC progression. Overall, CTSE expression and activity shows potential to detect PDAC and other pancreatic diseases. Further research is needed to fully understand its functions and potential translational applicability.

Idioma originalEnglish
Páginas (desde-hasta)951-956
Número de páginas6
PublicaciónPancreatology
Volumen19
N.º7
DOI
EstadoPublished - oct 2019

Nota bibliográfica

Publisher Copyright:
© 2019 IAP and EPC

Financiación

Research in this publication was supported by: the ORIEN Foundation (ZC-M), The National Pancreas Foundation (ZC-M), The National Cancer Institute (NCI) R01CA223204 (ZC-M), and by the NCI and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) under award number U01DK108327 (DC, ZC-M, PH). This work was also supported in part by the Pelotonia Fellowship Program (SK) and the OSUCCC-Kenyon Student Summer Program (MH). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or the Pelotonia Fellowship Program.

FinanciadoresNúmero del financiador
ORIEN Foundation
National Childhood Cancer Registry – National Cancer InstituteR01CA223204
National Institute of Diabetes and Digestive and Kidney DiseasesU01DK108327
National Pancreas Foundation

    ASJC Scopus subject areas

    • Endocrinology, Diabetes and Metabolism
    • Hepatology
    • Gastroenterology

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