Back to Search Start Over

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

Authors :
Mehterov, Nikolay
Kazakova, Maria
Sbirkov, Yordan
Vladimirov, Boyan
Belev, Nikolay
Yaneva, Galina
Todorova, Krassimira
Hayrabedyan, Soren
Sarafian, Victoria
Source :
Genes. Jul2021, Vol. 12 Issue 7, p1085. 1p.
Publication Year :
2021

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734425
Volume :
12
Issue :
7
Database :
Academic Search Index
Journal :
Genes
Publication Type :
Academic Journal
Accession number :
151565294
Full Text :
https://doi.org/10.3390/genes12071085