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Targeting LKB1 in cancer – exposing and exploiting vulnerabilities

The LKB1 tumour suppressor is a serine/threonine kinase that functions as master regulator of cell growth, metabolism, survival and polarity. LKB1 is frequently mutated in human cancers and research spanning the last two decades have begun decoding the cellular pathways deregulated following LKB1 in...

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Detalles Bibliográficos
Autores principales: Momcilovic, M, Shackelford, D B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647688/
https://www.ncbi.nlm.nih.gov/pubmed/26196184
http://dx.doi.org/10.1038/bjc.2015.261
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author Momcilovic, M
Shackelford, D B
author_facet Momcilovic, M
Shackelford, D B
author_sort Momcilovic, M
collection PubMed
description The LKB1 tumour suppressor is a serine/threonine kinase that functions as master regulator of cell growth, metabolism, survival and polarity. LKB1 is frequently mutated in human cancers and research spanning the last two decades have begun decoding the cellular pathways deregulated following LKB1 inactivation. This work has led to the identification of vulnerabilities present in LKB1-deficient tumour cells. Pre-clinical studies have now identified therapeutic strategies targeting this subset of tumours that promise to benefit this large patient population harbouring LKB1 mutations. Here, we review the current efforts that are underway to translate pre-clinical discovery of therapeutic strategies targeting LKB1 mutant cancers into clinical practice.
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spelling pubmed-46476882015-12-01 Targeting LKB1 in cancer – exposing and exploiting vulnerabilities Momcilovic, M Shackelford, D B Br J Cancer Minireview The LKB1 tumour suppressor is a serine/threonine kinase that functions as master regulator of cell growth, metabolism, survival and polarity. LKB1 is frequently mutated in human cancers and research spanning the last two decades have begun decoding the cellular pathways deregulated following LKB1 inactivation. This work has led to the identification of vulnerabilities present in LKB1-deficient tumour cells. Pre-clinical studies have now identified therapeutic strategies targeting this subset of tumours that promise to benefit this large patient population harbouring LKB1 mutations. Here, we review the current efforts that are underway to translate pre-clinical discovery of therapeutic strategies targeting LKB1 mutant cancers into clinical practice. Nature Publishing Group 2015-08-11 2015-07-21 /pmc/articles/PMC4647688/ /pubmed/26196184 http://dx.doi.org/10.1038/bjc.2015.261 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Minireview
Momcilovic, M
Shackelford, D B
Targeting LKB1 in cancer – exposing and exploiting vulnerabilities
title Targeting LKB1 in cancer – exposing and exploiting vulnerabilities
title_full Targeting LKB1 in cancer – exposing and exploiting vulnerabilities
title_fullStr Targeting LKB1 in cancer – exposing and exploiting vulnerabilities
title_full_unstemmed Targeting LKB1 in cancer – exposing and exploiting vulnerabilities
title_short Targeting LKB1 in cancer – exposing and exploiting vulnerabilities
title_sort targeting lkb1 in cancer – exposing and exploiting vulnerabilities
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647688/
https://www.ncbi.nlm.nih.gov/pubmed/26196184
http://dx.doi.org/10.1038/bjc.2015.261
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