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Signaling cascades are targets for breast cancer therapy in the light of genome – wide sequencing data

https://doi.org/10.17650/2313-805X-2025-12-1-8-13

Abstract

Development of next generation sequencing technologies allows to identify a large number of genetic landscape types in various cancers including breast cancer. Frequent genetic abnormalities identified using whole genome sequencing are point mutations (missense, nonsense mutations), deletions, insertions, which usually lead to activation of protooncogenes and inactivation of tumor suppressor genes. Genome sequencing of malignant tumors allowed, on one hand, to identify driver mutations in carcinogenic genes in different organs, and on the other – to use mutated genes for targeted therapy. Study of biological functions of these genes from the point of view of their contribution to carcinogenesis allows to better understand its mechanism. In this review, signaling cascades of breast cancer with identified mutated genes – targets for therapy – are analyzed.

About the Authors

L. F. Gulyaeva
Federal Research Center for Fundamental and Translational Medicine
Russian Federation

 Lyudmila Fyodorovna Gulyaeva 

2/12 Timakova St., Novosibirsk 630060, Russia 



M. L. Filipenko
Institute of Chemical Biology and Fundamental Medicine of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

8 Akademika Lavrentieva St., Novosibirsk 630090, Russia 



N. E. Kushlinskii
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Russian Federation

24 Kashirskoe Shosse, Moscow 115522, Russia 



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Review

For citations:


Gulyaeva L.F., Filipenko M.L., Kushlinskii N.E. Signaling cascades are targets for breast cancer therapy in the light of genome – wide sequencing data. Advances in Molecular Oncology. 2025;12(1):8-13. (In Russ.) https://doi.org/10.17650/2313-805X-2025-12-1-8-13

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ISSN 2313-805X (Print)
ISSN 2413-3787 (Online)