| Literature DB >> 25432020 |
Jia-Hao Jiang1, Chen Liu2, He Cheng1, Yu Lu2, Yi Qin2, Yong-Feng Xu1, Jin Xu1, Jiang Long1, Liang Liu1, Quan-Xing Ni1, Xian-Jun Yu3.
Abstract
Pancreatic cancer is one of the most aggressive solid malignancies. This aggressiveness is partly attributable to extensive local tumor invasion and early systemic dissemination as well as resistance to chemotherapy. Epithelial-mesenchymal transition (EMT) plays fundamental roles in embryonic development and in the differentiation of normal tissues and organs. EMT also plays critical roles in tumor formation, dissemination and drug resistance in pancreatic cancer. Emerging data suggest that inhibiting EMT may reverse the EMT phenotype and enhance the efficacy of chemotherapeutic agents against pancreatic cancer cells. Thus, an understanding of the molecular biology of EMT in pancreatic cancer may provide insights into the mechanisms of tumor invasion and metastatic progression and facilitate the development of alternative therapeutic approaches to improve the treatment outcomes for patients suffering from pancreatic cancer.Entities:
Keywords: Epithelial–mesenchymal transition; Metastasis; Pancreatic cancer; Prognosis; Therapy; Tumorigenesis
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Year: 2014 PMID: 25432020 DOI: 10.1016/j.bbcan.2014.11.004
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002