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Biliary tract cancers: current knowledge, clinical candidates and future challenges

Biliary tract cancers (BTCs) are rare with poor prognosis. Due to the advent of genomic sequencing, new data have emerged regarding the molecular makeup of this disease. To add to the complexity, various subtypes also harbor a varied genetic composition. The commonly mutated genes associated with th...

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Autores principales: Tariq, Noor-ul-Ain, McNamara, Mairéad G, Valle, Juan W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446989/
https://www.ncbi.nlm.nih.gov/pubmed/31015767
http://dx.doi.org/10.2147/CMAR.S157092
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author Tariq, Noor-ul-Ain
McNamara, Mairéad G
Valle, Juan W
author_facet Tariq, Noor-ul-Ain
McNamara, Mairéad G
Valle, Juan W
author_sort Tariq, Noor-ul-Ain
collection PubMed
description Biliary tract cancers (BTCs) are rare with poor prognosis. Due to the advent of genomic sequencing, new data have emerged regarding the molecular makeup of this disease. To add to the complexity, various subtypes also harbor a varied genetic composition. The commonly mutated genes associated with this cancer are KRAS, EGFR, IDH, FGFR and BAP1. Various clinical studies are looking at targeting these genetic mutations. Another therapeutic area of note is the potential for the use of immunotherapy in patients with BTC. Although BTC may be a result of chronic inflammation, this does not necessarily translate into increased immunogenicity. This literature review discusses the diverse molecular and immune-related pathways in patients with BTC and their potential therapeutic implications.
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spelling pubmed-64469892019-04-23 Biliary tract cancers: current knowledge, clinical candidates and future challenges Tariq, Noor-ul-Ain McNamara, Mairéad G Valle, Juan W Cancer Manag Res Review Biliary tract cancers (BTCs) are rare with poor prognosis. Due to the advent of genomic sequencing, new data have emerged regarding the molecular makeup of this disease. To add to the complexity, various subtypes also harbor a varied genetic composition. The commonly mutated genes associated with this cancer are KRAS, EGFR, IDH, FGFR and BAP1. Various clinical studies are looking at targeting these genetic mutations. Another therapeutic area of note is the potential for the use of immunotherapy in patients with BTC. Although BTC may be a result of chronic inflammation, this does not necessarily translate into increased immunogenicity. This literature review discusses the diverse molecular and immune-related pathways in patients with BTC and their potential therapeutic implications. Dove Medical Press 2019-03-29 /pmc/articles/PMC6446989/ /pubmed/31015767 http://dx.doi.org/10.2147/CMAR.S157092 Text en © 2019 Tariq et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Tariq, Noor-ul-Ain
McNamara, Mairéad G
Valle, Juan W
Biliary tract cancers: current knowledge, clinical candidates and future challenges
title Biliary tract cancers: current knowledge, clinical candidates and future challenges
title_full Biliary tract cancers: current knowledge, clinical candidates and future challenges
title_fullStr Biliary tract cancers: current knowledge, clinical candidates and future challenges
title_full_unstemmed Biliary tract cancers: current knowledge, clinical candidates and future challenges
title_short Biliary tract cancers: current knowledge, clinical candidates and future challenges
title_sort biliary tract cancers: current knowledge, clinical candidates and future challenges
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446989/
https://www.ncbi.nlm.nih.gov/pubmed/31015767
http://dx.doi.org/10.2147/CMAR.S157092
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