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Overcome Drug Resistance in Cholangiocarcinoma: New Insight Into Mechanisms and Refining the Preclinical Experiment Models

Overview
Journal Front Oncol
Specialty Oncology
Date 2022 Apr 4
PMID 35372014
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Abstract

Cholangiocarcinoma (CCA) is an aggressive tumor characterized by a poor prognosis. Therapeutic options are limited in patients with advanced stage of CCA, as a result of the intrinsic or acquired resistance to currently available chemotherapeutic agents, and the lack of new drugs entering into clinical application. The challenge in translating basic research to the clinical setting, caused by preclinical models not being able to recapitulate the tumor characteristics of the patient, seems to be an important reason for the lack of effective and specific therapies for CCA. So, there seems to be two ways to improve patient outcomes. The first one is developing the combination therapies based on a better understanding of the mechanisms contributing to the resistance to currently available chemotherapeutic agents. The second one is developing novel preclinical experimental models that better recapitulate the genetic and histopathological features of the primary tumor, facilitating the screening of new drugs for CCA patients. In this review, we discussed the evidence implicating the mechanisms underlying treatment resistance to currently investigated drugs, and the development of preclinical experiment models for CCA.

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References
1.
Khan S, Genus T, Morement H, Murphy A, Rous B, Tataru D . Global trends in mortality from intrahepatic and extrahepatic cholangiocarcinoma. J Hepatol. 2019; 71(6):1261-1262. DOI: 10.1016/j.jhep.2019.07.024. View

2.
Ikenoue T, Terakado Y, Nakagawa H, Hikiba Y, Fujii T, Matsubara D . A novel mouse model of intrahepatic cholangiocarcinoma induced by liver-specific Kras activation and Pten deletion. Sci Rep. 2016; 6:23899. PMC: 4817147. DOI: 10.1038/srep23899. View

3.
Hahnvajanawong C, Wattanawongdon W, Chomvarin C, Anantachoke N, Kanthawong S, Sripa B . Synergistic effects of isomorellin and forbesione with doxorubicin on apoptosis induction in human cholangiocarcinoma cell lines. Cancer Cell Int. 2015; 14:68. PMC: 4392878. DOI: 10.1186/1475-2867-14-68. View

4.
Spaeth E, Klopp A, Dembinski J, Andreeff M, Marini F . Inflammation and tumor microenvironments: defining the migratory itinerary of mesenchymal stem cells. Gene Ther. 2008; 15(10):730-8. DOI: 10.1038/gt.2008.39. View

5.
Miserocchi G, Mercatali L, Liverani C, De Vita A, Spadazzi C, Pieri F . Management and potentialities of primary cancer cultures in preclinical and translational studies. J Transl Med. 2017; 15(1):229. PMC: 5688825. DOI: 10.1186/s12967-017-1328-z. View