ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION

Introduction. As it is known, only 2 % of the human genome encodes proteins, while the greater part of the genome corresponds to non-coding sequences. In the recent years among a large variety of non-coding sequences special attention of researchers was drawn to long non-coding RNA MALAT1. This sequ...

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Main Authors: A. D. Volkogon, A. A. Roshchupkin, Ya. D Chumachenko, V. Yu. Harbuzova, A. V. Ataman
Format: Article
Language:English
Published: Sumy State University 2019-06-01
Series:Східноукраїнський медичний журнал
Subjects:
Online Access:https://eumj.med.sumdu.edu.ua/index.php/journal/article/view/18
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author A. D. Volkogon
A. A. Roshchupkin
Ya. D Chumachenko
V. Yu. Harbuzova
A. V. Ataman
author_facet A. D. Volkogon
A. A. Roshchupkin
Ya. D Chumachenko
V. Yu. Harbuzova
A. V. Ataman
author_sort A. D. Volkogon
collection DOAJ
description Introduction. As it is known, only 2 % of the human genome encodes proteins, while the greater part of the genome corresponds to non-coding sequences. In the recent years among a large variety of non-coding sequences special attention of researchers was drawn to long non-coding RNA MALAT1. This sequence first was detected in 2003 in non-small cell lung cancer cells. Today the results of numerous experiments revealed that MALAT1 is one of the major genes involved in various types of cancer, including kidney cancer. Purpose. To study the association between MALAT1 rs3200401 po­lymorphism and kidney cancer development in Ukrainian population. Materials and methods. 101 patients with kidney cancer (renal cell carcinoma) was enrolled into the study. The final diagnosis was based on anamnesis data, clinical, biochemical and instrumental examinations according to the recommendations of European Association of Urology. All participants were treated in the hospital of Sumy Regional Oncology Center. The control group included 100 healthy individuals without personal cancer history. The study of MALAT1 rs3200401 SNP was perfprmed by Real-time PCR using 7500 Fast Real-time PCR System (Applied Biosystems, Foster City, USA) and Taq-Man Assays (TaqMan®SNP Assay C_3246069_10). Statistical analyses were performed using Statistical Package for Social Science software (SPSS, version 17.0, Chicago, IL, USA) and online resource “SNIPKA”. Results. The distribution of CC-homozygotes, CT-heterozygotes and TT-homozygotes in patients with kidney cancer was 71 (70.3%), 29 (28.7 %) and 1 (0.99 %), respectively. In the control group, distribution of genotypes was 59 (59.0 %), 32 (32.0 %) and 9 (9.0 %), respectively. The significant difference in genotypes distribution between kidney cancer patients and the control group was found (P = 0.022). Genotypic analysis has shown that T-minor allele carriers had less risk of kidney cancer development compared to patients with CC-genotype (P = 0.031, OR = 0.101, 95 % CI = 0.013–0.814). Conclusion. There is statistically significant link between MALAT1 rs3200401 polymorphism and kidney cancer development in Ukrainian population. Individuals with minor T-allele (TT- and CT-genotypes) have less risk of renal cell carcinoma development compared to major homozygotes (CC).
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spelling doaj.art-f659a15601714b9baddc03dbfa9da5402022-12-22T03:42:45ZengSumy State UniversityСхідноукраїнський медичний журнал2663-59092664-42312019-06-0172121–125121–12518ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATIONA. D. Volkogon0A. A. Roshchupkin1Ya. D Chumachenko2V. Yu. Harbuzova3A. V. Ataman4Sumy State University, 2 Rimskogo-Korsakova str, Sumy, Ukraine, 40007Sumy State University, 2 Rimskogo-Korsakova str, Sumy, Ukraine, 40007Sumy State University, 2 Rimskogo-Korsakova str, Sumy, Ukraine, 40007Sumy State University, 2 Rimskogo-Korsakova str, Sumy, Ukraine, 40007Sumy State University, 2 Rimskogo-Korsakova str, Sumy, Ukraine, 40007Introduction. As it is known, only 2 % of the human genome encodes proteins, while the greater part of the genome corresponds to non-coding sequences. In the recent years among a large variety of non-coding sequences special attention of researchers was drawn to long non-coding RNA MALAT1. This sequence first was detected in 2003 in non-small cell lung cancer cells. Today the results of numerous experiments revealed that MALAT1 is one of the major genes involved in various types of cancer, including kidney cancer. Purpose. To study the association between MALAT1 rs3200401 po­lymorphism and kidney cancer development in Ukrainian population. Materials and methods. 101 patients with kidney cancer (renal cell carcinoma) was enrolled into the study. The final diagnosis was based on anamnesis data, clinical, biochemical and instrumental examinations according to the recommendations of European Association of Urology. All participants were treated in the hospital of Sumy Regional Oncology Center. The control group included 100 healthy individuals without personal cancer history. The study of MALAT1 rs3200401 SNP was perfprmed by Real-time PCR using 7500 Fast Real-time PCR System (Applied Biosystems, Foster City, USA) and Taq-Man Assays (TaqMan®SNP Assay C_3246069_10). Statistical analyses were performed using Statistical Package for Social Science software (SPSS, version 17.0, Chicago, IL, USA) and online resource “SNIPKA”. Results. The distribution of CC-homozygotes, CT-heterozygotes and TT-homozygotes in patients with kidney cancer was 71 (70.3%), 29 (28.7 %) and 1 (0.99 %), respectively. In the control group, distribution of genotypes was 59 (59.0 %), 32 (32.0 %) and 9 (9.0 %), respectively. The significant difference in genotypes distribution between kidney cancer patients and the control group was found (P = 0.022). Genotypic analysis has shown that T-minor allele carriers had less risk of kidney cancer development compared to patients with CC-genotype (P = 0.031, OR = 0.101, 95 % CI = 0.013–0.814). Conclusion. There is statistically significant link between MALAT1 rs3200401 polymorphism and kidney cancer development in Ukrainian population. Individuals with minor T-allele (TT- and CT-genotypes) have less risk of renal cell carcinoma development compared to major homozygotes (CC).https://eumj.med.sumdu.edu.ua/index.php/journal/article/view/18malat1, long non coding rna, single nucleotide polymorphism, renal cell carcinoma.
spellingShingle A. D. Volkogon
A. A. Roshchupkin
Ya. D Chumachenko
V. Yu. Harbuzova
A. V. Ataman
ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION
Східноукраїнський медичний журнал
malat1, long non coding rna, single nucleotide polymorphism, renal cell carcinoma.
title ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION
title_full ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION
title_fullStr ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION
title_full_unstemmed ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION
title_short ASSOCIATION OF MALAT1 RS3200401 GENE POLYMORPHISM WITH KIDNEY CANCER IN UKRAINIAN POPULATION
title_sort association of malat1 rs3200401 gene polymorphism with kidney cancer in ukrainian population
topic malat1, long non coding rna, single nucleotide polymorphism, renal cell carcinoma.
url https://eumj.med.sumdu.edu.ua/index.php/journal/article/view/18
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AT yadchumachenko associationofmalat1rs3200401genepolymorphismwithkidneycancerinukrainianpopulation
AT vyuharbuzova associationofmalat1rs3200401genepolymorphismwithkidneycancerinukrainianpopulation
AT avataman associationofmalat1rs3200401genepolymorphismwithkidneycancerinukrainianpopulation