Found: 11
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020
Fedorova P.A., Nazarov V.D., Musaelyan A.A., Lapin S.V., Boriskova M.E., Farafonova U.V., Emanuel V.L.
Introduction. Thyroid cancer (TC) is the most prevalent cancer among malignant neoplasms of the organs of the endocrine system. Cytological categories Bethesda III–V of TC are considered to be the most difficult for making a diagnosis. Molecular genetic tests …
ОБЗОР2020
Ruksha T.G., Zemtsov D.S., Lavrentiev S.N., Palkina N.V., Yessimbekova A.R.
Cutaneous melanoma is a highly heterogeneous malignancy, which characterized by low effectiveness of chemotherapeutic antitumor agents. 50% of melanomas have a somatic mutation in BRAF oncogene, leading to uncontrolled activation of mitogen-activated protein k…
ОБЗОР2019
Shirshova A.N., Boyarskikh U.A., Filipenko M.L., Pokrovsky V.S., Kushlinskii N.E.
The review highlights current data on molecular pathogenesis and potential markers of clear cell renal cell carcinoma, obtained in MultiOmyx studies. Key molecular mechanisms of the pathogenesis of RCC are the loss of functions of the VHL, PBRM1, SETD2, BAP1, …
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019
Musaelyan A.A., Chistyakov I.V., Nazarov V.D., Lapin S.V., Sogoyan M.V., Khalchitsky S.E., Emanuel W.L., Lobachevskaya T.W., Akopov A.L.
Background. Genotyping of the tumor samples is necessary for a personalized approach in the treatment of patients with malignancies. The identification of somatic mutations in EGFR and KRAS genes can help to predict the course of the disease and to individuali…
ОБЗОР2019
Spirina L.V., Slonimskaya E.M., Yurmazov Z.A., Usynin E.A., Lushnikova N.A., Tarasenko N.V., Kondakova I.V.
The review presents data on the role of the nuclear factor NF-κB and the von Hippel-Lindau protein (VHL) in the development of kidney cancer. Chemo- and radioresistance, specific for renal cell carcinoma, represented a significant problem in the treatment of p…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016
Kit O.I., Vodolazhsky D.I., Maksimov A.Yu., Lazutin Yu.N., Pyltsin S.P., Leyman I.A., Makueva A.M.
Introduction. EGFR mutation and EML4-ALK fusion are the most clinically significant genetic alterations in non-small cell lung cancer. Numerous studies have been devoted to EGFR mutations and their association with phenotypic clinical and pathological characte…
ОБЗОР2016
Mikhaylenko D.S., Kolpakov A.V., Kushlinskii N.E.
Renal cancer is among the most common oncourological diseases, and represents a heterogeneous group of tumors, which up to 80% is a clear cell renal cancer (CCRC). The study of rare hereditary forms of CCRC led to identification of the VHL gene; germinal VHL m…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015
Nemtsova M.V., Tanas A.S., Alekseeva E.A., Bykov I.I., Zaletayev D.V., Khorobrykh T.V., Strelnikov V.V.
Introduction. Most cases of gastric cancer (GC) occur sporadically. Until recently, diffuse hereditary gastric cancer associated with the CDH1 gene mutations was considered the only hereditary form (about 1–3% of all tumors of the stomach). However, a signific…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015
Gershtein E.S.
The key role in the achievement of the main goals of personalized medicine in oncology i.e. treatment choice according to patient’s individual characteristics and biological properties of the tumor belongs to tumor molecular markers characterizing the specific…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015
Pospekhova N.I., Shubin V.P., Tsukanov A.S., Kashnikov V.N., Frolov S.A., Achkasov S.I., Sushkov O.I., Shelygin Yu.A.
Introduction. Colorectal cancer (CRC) often metastasizes even if the tumor is small in size that is the main cause of death. Complex process of epithelial-mesenchymal transition (EMT) is required for dissemination of tumor cells. EMT leads to the transformatio…
Research article2013
Mazurenko N.N., Tsyganova I.V., Gagarin I.M., Chuev I.V., Mochalnikova V.V., Kolomeytseva A.A., Gorbunova V.A.
Last successful results in target therapy of cancer were achieved with different tyrosine kinases inhibitors (TKI). Target therapy of non-small cell lung cancer (NSCLC) with EGFR inhibitors gefitinib and erlotinib is effective only in patients with somatic mut…