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Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy

Almost all transcribed human genes undergo alternative RNA splicing, which increases the diversity of the coding and non-coding cellular landscape. The resultant gene products might have distinctly different and, in some cases, even opposite functions. Therefore, the abnormal regulation of alternati...

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Autores principales: Mehterov, Nikolay, Kazakova, Maria, Sbirkov, Yordan, Vladimirov, Boyan, Belev, Nikolay, Yaneva, Galina, Todorova, Krassimira, Hayrabedyan, Soren, Sarafian, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306420/
https://www.ncbi.nlm.nih.gov/pubmed/34356101
http://dx.doi.org/10.3390/genes12071085
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author Mehterov, Nikolay
Kazakova, Maria
Sbirkov, Yordan
Vladimirov, Boyan
Belev, Nikolay
Yaneva, Galina
Todorova, Krassimira
Hayrabedyan, Soren
Sarafian, Victoria
author_facet Mehterov, Nikolay
Kazakova, Maria
Sbirkov, Yordan
Vladimirov, Boyan
Belev, Nikolay
Yaneva, Galina
Todorova, Krassimira
Hayrabedyan, Soren
Sarafian, Victoria
author_sort Mehterov, Nikolay
collection PubMed
description Almost all transcribed human genes undergo alternative RNA splicing, which increases the diversity of the coding and non-coding cellular landscape. The resultant gene products might have distinctly different and, in some cases, even opposite functions. Therefore, the abnormal regulation of alternative splicing plays a crucial role in malignant transformation, development, and progression, a fact supported by the distinct splicing profiles identified in both healthy and tumor cells. Drug resistance, resulting in treatment failure, still remains a major challenge for current cancer therapy. Furthermore, tumor cells often take advantage of aberrant RNA splicing to overcome the toxicity of the administered chemotherapeutic agents. Thus, deciphering the alternative RNA splicing variants in tumor cells would provide opportunities for designing novel therapeutics combating cancer more efficiently. In the present review, we provide a comprehensive outline of the recent findings in alternative splicing in the most common neoplasms, including lung, breast, prostate, head and neck, glioma, colon, and blood malignancies. Molecular mechanisms developed by cancer cells to promote oncogenesis as well as to evade anticancer drug treatment and the subsequent chemotherapy failure are also discussed. Taken together, these findings offer novel opportunities for future studies and the development of targeted therapy for cancer-specific splicing variants.
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spelling pubmed-83064202021-07-25 Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy Mehterov, Nikolay Kazakova, Maria Sbirkov, Yordan Vladimirov, Boyan Belev, Nikolay Yaneva, Galina Todorova, Krassimira Hayrabedyan, Soren Sarafian, Victoria Genes (Basel) Review Almost all transcribed human genes undergo alternative RNA splicing, which increases the diversity of the coding and non-coding cellular landscape. The resultant gene products might have distinctly different and, in some cases, even opposite functions. Therefore, the abnormal regulation of alternative splicing plays a crucial role in malignant transformation, development, and progression, a fact supported by the distinct splicing profiles identified in both healthy and tumor cells. Drug resistance, resulting in treatment failure, still remains a major challenge for current cancer therapy. Furthermore, tumor cells often take advantage of aberrant RNA splicing to overcome the toxicity of the administered chemotherapeutic agents. Thus, deciphering the alternative RNA splicing variants in tumor cells would provide opportunities for designing novel therapeutics combating cancer more efficiently. In the present review, we provide a comprehensive outline of the recent findings in alternative splicing in the most common neoplasms, including lung, breast, prostate, head and neck, glioma, colon, and blood malignancies. Molecular mechanisms developed by cancer cells to promote oncogenesis as well as to evade anticancer drug treatment and the subsequent chemotherapy failure are also discussed. Taken together, these findings offer novel opportunities for future studies and the development of targeted therapy for cancer-specific splicing variants. MDPI 2021-07-18 /pmc/articles/PMC8306420/ /pubmed/34356101 http://dx.doi.org/10.3390/genes12071085 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mehterov, Nikolay
Kazakova, Maria
Sbirkov, Yordan
Vladimirov, Boyan
Belev, Nikolay
Yaneva, Galina
Todorova, Krassimira
Hayrabedyan, Soren
Sarafian, Victoria
Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy
title Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy
title_full Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy
title_fullStr Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy
title_full_unstemmed Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy
title_short Alternative RNA Splicing—The Trojan Horse of Cancer Cells in Chemotherapy
title_sort alternative rna splicing—the trojan horse of cancer cells in chemotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306420/
https://www.ncbi.nlm.nih.gov/pubmed/34356101
http://dx.doi.org/10.3390/genes12071085
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