| Literature DB >> 25450798 |
Sara Lucena1, Roberto Castro1, Courtney Lundin1, Amanda Hofstetter1, Amber Alaniz2, Montamas Suntravat1, Elda Eliza Sánchez3.
Abstract
Pancreatic cancer often has a poor prognosis, even when diagnosed early. Pancreatic cancer typically spreads rapidly and is rarely detected in its early stages, which is a major reason it is a leading cause of cancer death. Signs and symptoms may not appear until pancreatic cancer is quite advanced, and complete surgical removal is not possible. Furthermore, pancreatic cancer responds poorly to most chemotherapeutic agents. The importance of integrins in several cell types that affect tumor progression has made them an appealing target for cancer therapy. Some of the proteins found in the snake venom present a great potential as anti-tumor agents. In this study, we summarize the activity of two integrins antagonist, recombinant disintegrins mojastin 1 and viridistatin 2, on human pancreatic carcinoma cell line (BXPC-3). Both recombinant disintegrins inhibited some essential aspects of the metastasis process such as proliferation, adhesion, migration, and survival through apoptosis, making these proteins prominent candidates for the development of drugs for the treatment of pancreatic cancer.Entities:
Keywords: Cancer therapy; Disintegrins; Integrins antagonist; Pancreatic cancer
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Year: 2014 PMID: 25450798 PMCID: PMC4278407 DOI: 10.1016/j.toxicon.2014.11.228
Source DB: PubMed Journal: Toxicon ISSN: 0041-0101 Impact factor: 3.033