GENE POLYMORPHISM FOR CATECHOLAMINE METABOLIC ENZYMES AND DNA EXCISION REPAIR AS A PREDICTOR OF REPRODUCTIVE LOSSES
- Authors: Makarov O.V.1, Morozova K.V.1, Salnikova L.E.2, Hadzieva M.B.2, Goncharova V.S.1, Lutsenko N.N.1
-
Affiliations:
- N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
- N.I. Vavilov Institute of General Genetics, Russian Academy of Sciences
- Issue: No 2 (2015)
- Pages: 60-65
- Section: Articles
- URL: https://journals.eco-vector.com/0300-9092/article/view/247393
- ID: 247393
Cite item
Abstract
Full Text
About the authors
Oleg Vasilievich Makarov
N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
Email: profmakarov@mail.ru
MD, Professor, honored doctor of Russia, head of the Department of obstetrics and gynecology № 1 Moscow 117997, Ostrovityanova str. 1, Russia
Ksenia V. Morozova
N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
Email: morozovadk@mail.ru
post-graduate student of the Department of obstetrics and gynecology № 1 Moscow 117997, Ostrovityanova str. 1, Russia
Love Efimovna Salnikova
N.I. Vavilov Institute of General Genetics, Russian Academy of Sciences
Email: salnikova@vigg.ru
Dr. Biol. Sci., leading researcher, laboratory of ecological genetics Moscow, Gubkina str. 3, Russia
Maryam Borisovna Hadzieva
N.I. Vavilov Institute of General Genetics, Russian Academy of Sciencesgraduate student, Junior researcher Moscow, Gubkina str. 3, Russia
Varvara Sergeevna Goncharova
N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
Email: v_seredenina@mail.ru
post-graduate student of the Department of obstetrics and gynecology № 1 Moscow 117997, Ostrovityanova str. 1, Russia
Nikolai Nikolaevich Lutsenko
N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
Email: lnn55@mail.ru
PhD, associate Professor of obstetrics and gynecology № 1 Moscow 117997, Ostrovityanova str. 1, Russia
References
- Сидельникова В.М. Подготовка и ведение беременности у женщин с привычным невынашиванием. Методические пособия и клинические протоколы. М.: МЕДпресс-информ; 2010. 219 с.
- Макаров О.В., Ковальчук Л.В., Ганковская Л.В., Бахарева И.В., Ганковская О.А. Невынашивание беременности, инфекция, врожденный иммунитет. Монография. М.: ГЭОТАР-Медиа; 2007.
- Сидельникова В.М. Неполноценная лютеиновая фаза (НЛФ) - тактика ведения женщин с привычной потерей беременности. В кн.: Привычная потеря беременности - новый взгляд на роль половых гормонов: Тезисы Всероссийского форума «Мать и дитя». М.; 2002: 907-8.
- Сидельникова В.М. Привычная потеря беременности. М.: Триада - X; 2002. 304 с.
- Feng Y., Zhao X., Zhou C., Yang L., Liu Y., Bian C. et al. The associations between the Val158Met in the catechol-O-methyltransferase (COMT) gene and the risk of uterine leiomyoma (ULM). Gene. 2013; 529(2): 296-9.
- Su Y., Xu A., Zhu J. The effect of oxoguanine glycosylase 1 rs1052133 polymorphism on colorectal cancer risk in Caucasian population.Tumour Biol. 2014; 35(1): 513-7.
- Середа Е. Е., Кондакова И. В., Слонимская Е. М. Ферменты метаболизма эстрогенов и рецепторы как факторы риска развития и прогноза при раке молочной железы. Сибирский онкологический журнал. 2004; 1: 35-43.
- Zhang J., Zhou J., Zhang P., Wang W., Tao S., Wang M. A meta-analysis of the association between the hOGG1 Ser326Cys polymorphism and the risk of esophageal squamous cell carcinoma. PLoS One. 2013; 8(6): e65742.
- Сальникова Л.Е., Чумаченко А.Г., Веснина И.Н., Лаптева Н.Ш., Кузнецова Г.И., Абилев С.К., Рубанович А.В. Полиморфизм генов репарации и цитогенетические эффекты облучения. Радиационная биология. Радиоэкология. 2010; 50(6): 656-62.
- Millikan R.C., Pittman G.S., Tse C.K., Duell E., Newman В., Savitz D., Bell D.A. Catechol-O-methyltransferase and breast cancer risk. Carcinogenesis. 1998; 19: 1943-7.
- Woo J.M., Yoon K.S., Yu B.H. Catechol O-methyltransferase genetic polymorphism in panic disorder. Am. J. Psychiatry. 2002; 159(10): 1785-7.
- Hamajima N. PCR-CTPP: a new genotyping technique in the era of geneti- cepidemiology. Expert. Rev. Mol. Diagn. 2001; 1: 119-23.
- Corvol J.-C., Bonnet C., Charbonnier-BeaupelF., BonnetA.-M., Fievet M.-H., Bellanger A. et al.The COMT Val158Met polymorphism affects the response to entacapone in Parkinson’s disease: a randomized crossover clinical trial. Ann. Neurol. 2011; 69: 111-8.
- Domschke K., Tidow N., Schrempf M., Schwarte K., Klauke B., Reif A. et al. Epigenetic signature of panic disorder: a role of glutamate decarboxylase 1 (GAD1) DNA hypomethylation? Prog. Neuropsychopharmacol. Biol. Psychiatry. 2013; 46: 189-96.
- Salnikova L, Chumachenko A., Belopolskaya O., Rubanovich A. Correlations between DNA polymorphism and frequencies of gamma-radiation induced and spontaneous cytogenetic damage. Health Phys. 2012; 103(1): 37-41.
- Sun C., Liu X., Zhang H., Guo W., Cai Z., Chen H. et al. Functional polymorphism of hOGG1 gene is associated with type 2 diabetes mellitus in Chinese population. Mol. Cell. Endocrinol. 2010; 325(1-2): 128-34.
- Chen X., Wang J., Guo W., Liu X., Sun C., Cai Z. et al. Two functional variations in 5’-UTR of hoGG1 gene associated with the risk of breast cancer in Chinese. Breast Cancer Res. Treat. 2011; 127(3): 795-803.