M.L. Filipenko –

Ph.D. (Biol.), Head of Pharmacogenomics Laboratory, Institute of Chemical Biology and Fundamental Medicine,

Siberian Branch of the Russian Academy of Sciences (Novosibirsk)

E-mail: max@niboch.nsc.ru

O.V. Somonova –

Dr.Sc. (Med.), Professor, N.N. Blokhin National Medical Research Center of Oncology of the Ministry

of Health of Russia (Moscow)

A.L. Elizarova –

Ph.D. (Biol.), N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Health

of Russia (Moscow)

N.E. Kushlinskii –

Dr.Sc. (Med.), Professor, Academician RAS, Head of the Laboratory of Clinical Biochemistry N.N. Blokhin

National Medical Research Center of Oncology of the Ministry of Health of Russia (Moscow)

Venous thromboembolism (VTE) is a common cardiovascular disease that results from a complex interaction between acquired

and hereditary factors. A study of the role of the genetic component in recent decades has revealed a number of significant

structural genetic variants that increase the risk of developing VET, among which the most studied ones are F5

rs6025, F2 rs1799963, FGG rs2066865, and AB0 blood groups. Genetic loci of predisposition to VET can also increase its likelihood

for cancer, which requires careful consideration to assess the possibility of their determination for clinical purposes.

Purpose of the study – the current state of studies devoted to the risk formation of venous thromboembolism (VTE) in cancer

diseases, taking into account genetic factors.

Search and critically evaluate relevant publications in the PubMed database.

The PubMed database was analyzed using following keywords: “cancer”, “oncological”, “thromboembolism”, “trombosis”,

“polymorphism”, “SNP”, “mutation”, “association”. 238 relevant publications were identified and critically evaluated.

Genetic factors make a significant additive contribution to the risk of VTE in patients with cancer, which makes them potential

prognostic biomarkers for improving the effectiveness of thromboprophylaxis based on the individual risk of the patient.

However, for most well-studied genetic markers of the population risk of VTE, their role in the formation of this type of risk in

cancer is characterized as either limited or insufficient, which requires further studies, adequately planned in design and representativeness.

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