分子遗传学方法在高癌症危险因素个体中有效检测遗传性癌症的能力

A.  B. Semenova, M. Byakhova, V. Galkin, Sergey A. Parts, M. Makarova, M. Nemtsova, D. Chernevskiy, O. Sagaydak, E. Baranova, M. Belenikin, A. Krinitsina, I. Khatkov, N. Bodunova, A. Danishevich, D. Kanner, N. Savelov, A. Shabunin, S. S. Lebedev, D. Protsenko, S. Gadzhieva
{"title":"分子遗传学方法在高癌症危险因素个体中有效检测遗传性癌症的能力","authors":"A.  B. Semenova, M. Byakhova, V. Galkin, Sergey A. Parts, M. Makarova, M. Nemtsova, D. Chernevskiy, O. Sagaydak, E. Baranova, M. Belenikin, A. Krinitsina, I. Khatkov, N. Bodunova, A. Danishevich, D. Kanner, N. Savelov, A. Shabunin, S. S. Lebedev, D. Protsenko, S. Gadzhieva","doi":"10.47619/2713-2617.zm.2023.v.4i2;30-40","DOIUrl":null,"url":null,"abstract":"Russia and other countries report an increase in the incidence of malignant neoplasms, and approximately 10 % of all oncological cases have hereditary background. Molecular genetic testing in patients with diagnosed malignant neoplasms and a suspected hereditary factor will help to select effective modern methods of treatment and prevention of the development of neoplasms of other localizations. \nAccording to the study, 12,6 % of patients had hereditary cancer syndrome, which allowed to administer molecular genetic tests to patients’ relatives. Consequently, it becomes possible to detect hereditary cancer risk factors, improve the efficiency of clinical examination, elaborate and implement programs for prevention and early detection of the disease.","PeriodicalId":158882,"journal":{"name":"City Healthcare","volume":"65 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Capabilities of Molecular Genetic Methods for Effective Hereditary Cancers Detection in Individuals with High Cancer Risk Factors\",\"authors\":\"A.  B. Semenova, M. Byakhova, V. Galkin, Sergey A. Parts, M. Makarova, M. Nemtsova, D. Chernevskiy, O. Sagaydak, E. Baranova, M. Belenikin, A. Krinitsina, I. Khatkov, N. Bodunova, A. Danishevich, D. Kanner, N. Savelov, A. Shabunin, S. S. Lebedev, D. Protsenko, S. Gadzhieva\",\"doi\":\"10.47619/2713-2617.zm.2023.v.4i2;30-40\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Russia and other countries report an increase in the incidence of malignant neoplasms, and approximately 10 % of all oncological cases have hereditary background. Molecular genetic testing in patients with diagnosed malignant neoplasms and a suspected hereditary factor will help to select effective modern methods of treatment and prevention of the development of neoplasms of other localizations. \\nAccording to the study, 12,6 % of patients had hereditary cancer syndrome, which allowed to administer molecular genetic tests to patients’ relatives. Consequently, it becomes possible to detect hereditary cancer risk factors, improve the efficiency of clinical examination, elaborate and implement programs for prevention and early detection of the disease.\",\"PeriodicalId\":158882,\"journal\":{\"name\":\"City Healthcare\",\"volume\":\"65 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"City Healthcare\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.47619/2713-2617.zm.2023.v.4i2;30-40\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"City Healthcare","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47619/2713-2617.zm.2023.v.4i2;30-40","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

俄罗斯和其他国家报告恶性肿瘤发病率增加,大约10%的肿瘤病例有遗传背景。对诊断为恶性肿瘤并怀疑有遗传因素的患者进行分子基因检测,将有助于选择有效的现代治疗方法和预防其他部位肿瘤的发展。根据这项研究,12.6%的患者患有遗传性癌症综合征,这使得对患者亲属进行分子基因测试成为可能。因此,有可能发现遗传性癌症危险因素,提高临床检查的效率,制定和实施预防和早期发现疾病的方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Capabilities of Molecular Genetic Methods for Effective Hereditary Cancers Detection in Individuals with High Cancer Risk Factors
Russia and other countries report an increase in the incidence of malignant neoplasms, and approximately 10 % of all oncological cases have hereditary background. Molecular genetic testing in patients with diagnosed malignant neoplasms and a suspected hereditary factor will help to select effective modern methods of treatment and prevention of the development of neoplasms of other localizations. According to the study, 12,6 % of patients had hereditary cancer syndrome, which allowed to administer molecular genetic tests to patients’ relatives. Consequently, it becomes possible to detect hereditary cancer risk factors, improve the efficiency of clinical examination, elaborate and implement programs for prevention and early detection of the disease.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Organizational And Social Technologies For Early Cancer Detection Among General Population Mathematical Modeling Of The Active Life Expectancy Among The Famous Soviet Mathematicians Medical and Social Characteristics of Living Conditions, Lifestyle, and Motivation to Become a Doctor among Students and Residents of Medical University Adherence To Healthy Lifestyle Among Medical Workers In Routine Practice And During The COVID-19 Pandemic Abroad Digitalization Of Document Management System In Medical Organizations: Theoretical Aspect
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1