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Value of genetic testing of herminal tumor mutations in screening and prevention of malignant formations

Abstract

The authors analyzed available data in modern literature on the role of genetic testing for mutations in genes responsible for predisposing to hereditary cancers of reproductive organs in women. They are looking at data on the importance of using genetic testing in clinical practice to predict the disease development, need for follow-up monitoring in the presence of mutation load, and determination of combined chemotherapy policy for malignant neoplasms.

About the Authors

O. A. Buyanovskaya
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


O. V. Burmenskaya
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


А. . Goltsov
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


T. . Kochetkova
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


J. . Shubina
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


N. . Mishina
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


D. Yu. Trofimov
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Russian Federation


Review

For citations:


Buyanovskaya O.A., Burmenskaya O.V., Goltsov А., Kochetkova T., Shubina J., Mishina N., Trofimov D.Yu. Value of genetic testing of herminal tumor mutations in screening and prevention of malignant formations. Medical Genetics. 2020;19(6):40-41. (In Russ.)

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ISSN 2073-7998 (Print)