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Molecular Medicine Peer-reviewed scientific journal

Found: 11

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020

STANDARDIZATION OF THE METHOD OF MULTI-TARGET SINGLE-NUCLEOTIDE ELONGATION FOR MOLECULAR GENETIC STUDY OF CYTOLOGICAL MATERIAL IN THYROID NEOPLASM

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 …

10.29296/24999490-2020-06-05Details ↗
ОБЗОР2020

MOLECULAR MECHANISMS OF RESISTANCE DEVELOPMENT UNDER TARGETED THERAPY ON THE EXAMPLE OF CUTANEOUS MELANOMA

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…

10.29296/24999490-2020-06-02Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

OPTIMIZATION OF THE METHOD OF THE MULTI-TARGET SINGLE-BASE ELONGATION FOR THE DETECTION OF SOMATIC MUTATIONS IN MALIGNANCIES

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…

10.29296/24999490-2019-02-06Details ↗
ОБЗОР2019

THE ROLE OF NF-κB AND von HIPPEL-LINDAU PROTEIN IN THE CREATION OF A MOLECULAR PORTRAIT OF KIDNEY CANCERS

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…

10.29296/24999490-2019-03-03Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

MOLECULAR GENETIC AND PHENOTYPIC CHARACTERISTICS OF PATIENTS WITH LUNG ADENOCARCINOMA AMONG INHABITANTS OF THE SOUTH OF RUSSIA

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…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

SOMATIC AND GERMLINE MUTATIONS IN GASTRIC CANCER

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…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

EPITHELIAL-MESENCHYMAL TRANSITION IN COLORECTAL CANCER OF DIFFERENT STAGES

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…

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Research article2013

EGFR AND KRAS MUTATIONS IMPORTANT FOR NON-SMALL CELL LUNG CANCER TARGET THERAPY

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…

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