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MODELING OF A SUBCUTANEOUS XENOGRATF OF HUMAN MELANOMA SKIN MEL RAC WITH NRAS MUTATION ON IMMUNODEFICIENT MICE FOR PRECLINICAL STUDYING THE TARGETING ANTICANCER DRUGS

https://doi.org/10.17650/1726-9784-2016-15-3-40-46

Abstract

Background. Development of new models of a human disseminative melanoma of skin with existence of a molecular and genetic target for specific therapy increases productivity of the preclinical researches in vitro and in vivo new the anti-melanoma drugs or their combinations. Such opportunity is realized by adaptation to in vivo of the original human pigment-free skin melanoma cell line mel Rac and receiving s. c. xenograft under monitoring, transplant, morphological, molecular and genetic (NRAS mutation) and chemotherapeutic (sensitivity to an inhibitor of NRAS a trametinib) characteristics. Objective. Receiving from the cell line mel Rac s. c. xenograft of a human pigmented melanoma of skin with a mutation of NRAS and sensitive to specific target therapy. Materials and methods. Human pigment-free skin melanoma cell line mel Rac from the Collection of Russian Cancer Research Center and immunodeficient female of Balb/c nude mice cultivation of Russian Cancer Research Center was used. Required characteristics are defined at a multiple s. c. transplanting in vivo by methods of transplant biology, a light microscopy, molecular genetics and the experimental chemotherapy. Sensitivity to a NRAS inhibitor to a trametinib was estimated under monitoring of rate of the tumor growth (Vt/V0) on indexes, adequate for patients: existence of the complete remission and possibility of recurrence. Results. At s. c. transplantation of 107 cell of mel Rac line are received cytological identical intertwined s. c. xenografts with a stable kinetics of growth on 4-9 passages (a latent phase 8 days, exponential - to 14 days, stationary - to 24 days) and existence of a mutation of NRAS. Trametinib in a single dose of 0,3 mg/kg caused the complete remission during a 14-day course and within 7 days after its cancellation without recurrence. Conclusion. Receiving with cell line mel Rac s. c. xenograft of a human pigment-free melanoma of skin with a mutation of NRAS and sensitive to specific target therapy is suitable for preclinical studying of the specific for this target new anti-melanoma drugs.

About the Authors

N. V. Andronova
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


S. M. Sitdikova
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


L. F. Morozova
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


A. A. Lushnikova
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


D. A. Ponkratova
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


I. N. Mikhailova
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


N. T. Raychlin
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


I. A. Bukaeva
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


H. M. Treshalina
ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России
Russian Federation


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Review

For citations:


Andronova N.V., Sitdikova S.M., Morozova L.F., Lushnikova A.A., Ponkratova D.A., Mikhailova I.N., Raychlin N.T., Bukaeva I.A., Treshalina H.M. MODELING OF A SUBCUTANEOUS XENOGRATF OF HUMAN MELANOMA SKIN MEL RAC WITH NRAS MUTATION ON IMMUNODEFICIENT MICE FOR PRECLINICAL STUDYING THE TARGETING ANTICANCER DRUGS. Russian Journal of Biotherapy. 2016;15(3):40-46. (In Russ.) https://doi.org/10.17650/1726-9784-2016-15-3-40-46

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ISSN 1726-9784 (Print)
ISSN 1726-9792 (Online)