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dc.creatorChen, C. (Chaobo)-
dc.creatorNelson, L.J. (Leonard J.)-
dc.creatorAvila, M.A. (Matías Antonio)-
dc.creatorCubero, F.J. (Francisco Javier)-
dc.date.accessioned2021-10-07T10:39:55Z-
dc.date.available2021-10-07T10:39:55Z-
dc.date.issued2019-
dc.identifier.citationChen, C. (Chaobo); Nelson, L.J. (Leonard J.); Avila, M.A. (Matías Antonio); et al. "Mitogen-activated protein kinases (MAPKs) and cholangiocarcinoma: the missing Link". Cells. 8 (10), 2019,es_ES
dc.identifier.issn2073-4409-
dc.identifier.urihttps://hdl.handle.net/10171/62156-
dc.description.abstractIn recent years, the incidence of both liver and biliary tract cancer has increased. Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) are the two most common types of hepatic malignancies. Whereas HCC is the fifth most common malignant tumor in Western countries, the prevalence of CCA has taken an alarming increase from 0.3 to 2.1 cases per 100,000 people. The lack of specific biomarkers makes diagnosis very difficult in the early stages of this fatal cancer. Thus, the prognosis of CCA is dismal and surgery is the only effective treatment, whilst recurrence after resection is common. Even though chemotherapy and radiotherapy may prolong survival in patients with CCA, the 5-year survival rate is still very low—a significant global problem in clinical diagnosis and therapy. The mitogen-activated protein kinase (MAPK) pathway plays an important role in signal transduction by converting extracellular stimuli into a wide range of cellular responses including inflammatory response, stress response, differentiation, survival, and tumorigenesis. Dysregulation of the MAPK cascade involves key signaling components and phosphorylation events that play an important role in tumorigenesis. In this review, we discuss the pathophysiological role of MAPK, current therapeutic options, and the current situation of MAPK-targeted therapies in CCA.es_ES
dc.description.sponsorshipThis work was supported by the MINECO Retos SAF2016-78711, EXOHEP-CM S2017/BMD-3727, NanoLiver-CM Y2018/NMT-4949, UCM-25-2019, ERAB EA/18-14, AMMF 2018/117, and COST Action CA17112. We also acknowledge the funding from the Instituto de Salud Carlos III grant FIS16/01126, AECC grant for rare tumors 2017, Hepacare Project “la Caixa”, and Gobierno de Navarra Salud Grant 58/17. F.J.C. is a Ramón y Cajal Researcher (RYC-2014-15242) affiliated with the UCM group “Lymphocyte Immunobiology”, No. 920631 (imas12-associated, Ref. IBL-6) and a Gilead Liver Research Scholar 2018.es_ES
dc.language.isoenges_ES
dc.publisherMDPI AGes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectCholangiocarcinoma (CCA)es_ES
dc.subjectMitogen-activated protein kinases (MAPK)es_ES
dc.subjectCholangiocyteses_ES
dc.subjectHepatocyteses_ES
dc.subjectEpithelial to mesenchymal transition (EMT)es_ES
dc.subjectCancer-associated fibroblasts (CAFs)es_ES
dc.titleMitogen-activated protein kinases (MAPKs) and cholangiocarcinoma: the missing Linkes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.3390/cells8101172-
dadun.citation.number10es_ES
dadun.citation.publicationNameCellses_ES
dadun.citation.volume8es_ES

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