4.6 Review

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

Journal

GENES
Volume 12, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/genes12071085

Keywords

alternative splicing; splice variants; cancer pathobiology; drug resistance

Funding

  1. Bulgarian Ministry of Science [KP-06-M, 23/1, KP-06-N33/4]
  2. Project NUCBAS-BBMRI.BG (Ministry of Education and Science) [D01-395/18.12.2020]

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Alternative RNA splicing is a crucial mechanism in gene regulation, with abnormal regulation playing a role in disease development. Targeting RNA splicing variants in tumor cells may offer new avenues for cancer treatment. Understanding splicing variants in cancer cells could provide insights for designing more effective therapeutic approaches.
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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