Role of Alternative Splicing in Oncogenesis
https://doi.org/10.33647/2074-5982-20-3-130-135
Abstract
Over the past two decades, much evidence has accumulated that confirms the crucial role of alternative splicing in the process of tumorigenesis. A more detailed study of splicing mechanisms revealed that targeting the central process for atypical cells could be a potential new approach in the treatment of malignant neoplasms. Firstly, specific protein isoforms that are formed as a result of alternative splicing and are involved in tumorigenesis can potentially act as a target for the treatment of malignant neoplasms. Second, high rates of cell proliferation presumably make tumor cells highly dependent on a functional spliceosome, creating potential hypersensitivity to global splicing modulation. The study of the role of alternative splicing in tumorigenesis and the search for therapeutic targets contributed not only to the development of a more promising direction in oncology, but also to the search for new drugs that have a targeted effect on the development of malignant neoplasms.
About the Authors
O. M. KudelinaRussian Federation
Oksana M. Kudelina*, Cand. Sci. (Med.)
344022, Rostov-on-Don, Nakhichevansky Lane, 29
A. V. Safronenko
Russian Federation
Andrey V. Safronenko, Dr. Sci. (Med.), Prof.
344022, Rostov-on-Don, Nakhichevansky Lane, 29
M. Kh.-B. Burayeva
Russian Federation
Maret Kh.-B. Burayeva
344022, Rostov-on-Don, Nakhichevansky Lane, 29
M. Kh.-B. Burayeva
Russian Federation
Malika Kh.-B. Burayeva
344037, Rostov-on-Don, 14th Liniya Str., 63
S. A. Velichko
Russian Federation
Sofia A. Velichko
344022, Rostov-on-Don, Nakhichevansky Lane, 29
D. Terekhova
Russian Federation
Diana A. Terekhova
344022, Rostov-on-Don, Nakhichevansky Lane, 29
N. S. Benderskii
Russian Federation
Nikita S. Benderskii
344022, Rostov-on-Don, Nakhichevansky Lane, 29
A. A. Tolstoy
Russian Federation
Artem A. Tolstoy
344022, Rostov-on-Don, Nakhichevansky Lane, 29
References
1. Abramowicz A., Gos M. Splicing mutations in human genetic disorders: examples, detection, and confirmation. J. Appl. Genet. 2018;59(3):253–268. DOI: 10.1007/s13353-018-0444-7
2. Bessa C., Matos P., Jordan P., Gonçalves V. Alternative splicing: Expanding the landscape of cancer biomarkers and therapeutics. Int. J. Mol. Sci. 2020;21(23):9032. DOI: 10.3390/ijms21239032
3. Bradley R.K., Anczuków O. RNA splicing dysregulation and the hallmarks of cancer. Nat. Rev. Cancer. 2023;23(3):135–155. DOI: 10.1038/s41568-022-00541-7
4. Chen S., Benbarche S., Abdel-Wahab O. Splicing factor mutations in hematologic malignancies. Blood. 2021;138(8):599–612. DOI: 10.1182/blood.2019004260
5. Dalton W.B., Helmenstine E., Pieterse L., Li B., Gocke C.D., Donaldson J., Xiao Z., Gondek L.P., Ghiaur G., Gojo I., Smith B.D., Levis M.J., DeZern A.E. The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing. Blood Adv. 2020;4(7):1192–1196. DOI: 10.1182/bloodadvances.2019001127
6. Ghigna C., Paronetto M.P. Alternative splicing: Recent insights into mechanisms and functional roles. Cells. 2020;9(10):2327. DOI: 10.3390/cells9102327
7. Jayasinghe R.G., Cao S., Gao Q., Wendl M.C., Vo N.S., Reynolds S.M., Zhao Y., Climente-González H., Chai S., Wang F., Varghese R., Huang M., Liang W.W., Wyczalkowski M.A., Sengupta S., Li Z., Payne S.H., Fenyö D., Miner J.H., Walter M.J.; Cancer Genome Atlas Research Network; Vincent B., Eyras E., Chen K., Shmulevich I., Chen F., Ding L. Systematic analysis of splice-site-creating mutations in cancer. Cell Rep. 2018;23(1):270–281.e3. DOI: 10.1016/j.celrep.2018.03.052
8. Jiang M., Chen M., Liu Q., Jin Z., Yang X., Zhang W. SF3B1 mutations in myelodysplastic syndromes: A potential therapeutic target for modulating the entire disease process. Front. Oncol. 2023;13:1116438. DOI: 10.3389/fonc.2023.1116438
Review
For citations:
Kudelina O.M., Safronenko A.V., Burayeva M.Kh., Burayeva M.Kh., Velichko S.A., Terekhova D., Benderskii N.S., Tolstoy A.A. Role of Alternative Splicing in Oncogenesis. Journal Biomed. 2024;20(3):130-135. (In Russ.) https://doi.org/10.33647/2074-5982-20-3-130-135