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The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer

Gene fusions occur in up to 17% of solid tumours. Oncogenic kinases are often involved in such fusions. In lung cancer, almost 30% of patients carrying an activated oncogene show the fusion of a tyrosine kinase to an heterologous gene. Several genes are partner in the fusion with the three kinases A...

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Autores principales: Cerrato, Aniello, Visconti, Roberta, Celetti, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817729/
https://www.ncbi.nlm.nih.gov/pubmed/29455670
http://dx.doi.org/10.1186/s12943-018-0799-8
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author Cerrato, Aniello
Visconti, Roberta
Celetti, Angela
author_facet Cerrato, Aniello
Visconti, Roberta
Celetti, Angela
author_sort Cerrato, Aniello
collection PubMed
description Gene fusions occur in up to 17% of solid tumours. Oncogenic kinases are often involved in such fusions. In lung cancer, almost 30% of patients carrying an activated oncogene show the fusion of a tyrosine kinase to an heterologous gene. Several genes are partner in the fusion with the three kinases ALK, ROS1 and RET in lung. The impaired function of the partner gene, in combination with the activation of the kinase, may alter the cell signaling and promote the cancer cell addiction to the oncogene. Moreover, the gene that is partner in the fusion to the kinase may affect the response to therapeutics and/or promote resistance in the cancer cells. Few genes are recurrent partners in tyrosine kinase fusions in lung cancer, including CCDC6, a recurrent partner in ROS1 and RET fusions, that can be selected as possible target for new strategies of combined therapy including TKi.
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spelling pubmed-58177292018-02-23 The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer Cerrato, Aniello Visconti, Roberta Celetti, Angela Mol Cancer Review Gene fusions occur in up to 17% of solid tumours. Oncogenic kinases are often involved in such fusions. In lung cancer, almost 30% of patients carrying an activated oncogene show the fusion of a tyrosine kinase to an heterologous gene. Several genes are partner in the fusion with the three kinases ALK, ROS1 and RET in lung. The impaired function of the partner gene, in combination with the activation of the kinase, may alter the cell signaling and promote the cancer cell addiction to the oncogene. Moreover, the gene that is partner in the fusion to the kinase may affect the response to therapeutics and/or promote resistance in the cancer cells. Few genes are recurrent partners in tyrosine kinase fusions in lung cancer, including CCDC6, a recurrent partner in ROS1 and RET fusions, that can be selected as possible target for new strategies of combined therapy including TKi. BioMed Central 2018-02-19 /pmc/articles/PMC5817729/ /pubmed/29455670 http://dx.doi.org/10.1186/s12943-018-0799-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Cerrato, Aniello
Visconti, Roberta
Celetti, Angela
The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer
title The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer
title_full The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer
title_fullStr The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer
title_full_unstemmed The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer
title_short The rationale for druggability of CCDC6-tyrosine kinase fusions in lung cancer
title_sort rationale for druggability of ccdc6-tyrosine kinase fusions in lung cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817729/
https://www.ncbi.nlm.nih.gov/pubmed/29455670
http://dx.doi.org/10.1186/s12943-018-0799-8
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