Genetic Susceptibility to Infection Related Cancer

对感染相关癌症的遗传易感性

• 批准号: 6879629
• 负责人: IKUKO KATO
• 金额: $ 11.21万
• 依托单位: WAYNE STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-02-01 至 2008-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6879629
• 关键词: Helicobacter; achlorhydria; bacteria infection mechanism; bacterial cytopathogenic effect; clinical research; cytokine; gene environment interaction; genetic polymorphism; genetic susceptibility; genotype; host organism interaction; human tissue; infection related neoplasm /cancer; lipopolysaccharides; metaplasia; monocyte; neoplasm /cancer genetics; nucleic acid purification; polymerase chain reaction; statistics /biometry

DESCRIPTION (provided by applicant): The long-term goal of the proposed study is to provide a scientific basis to develop efficient primary prevention strategies against infection/inflammation-related cancers. Mounting evidence suggests that a variety of infectious agents have a role in the pathogenesis of human cancers. It is estimated that 15.6 percent of the worldwide cancer incidences in 1990 can be attributed to these infectious agents, accounting for a total of 1,450,000 cases. Helicobacter pylori (HP) is ranked top among various infectious agents and represents approximately 5 percent of new cancer cases in the world. These cancers are important from a public health point of view because they are potentially preventable by antibiotics treatment or vaccination. Whereas HP infection is very common (80-90 percent) in populations with high risk for stomach cancer, it is known that only a very small fraction of the population infected with HP actually develops cancer, suggesting a role for genetic components in HP-related carcinogenesis in addition to that of environmental co-factors. This proposal will specifically focus on the 2 groups of polymorphic genes, receptors to HP lipopolysaccharide (LPS), a cell wall component, which elicits immediate proinflammatory responses, (1) CD14 (C-260T), (2) TRL4 (A896G) and (3) NOD2 (3020insC); and resultant cytokines, (4) IL-8 (T-251A), (5) MCP1 (G-2518A), (6) IL-lbeta (T-31C) and (7) TNF-alpha (G-308A). These polymorphic genes are known to be functional and have been postulated to modify host responses to HP infection. The proposed study will be designed as a spin-off study of a chemo prevention trial for gastric cancer in Venezuela, taking advantage of unique characteristics of the study population, i.e., a strikingly high (95 percent) HP infection rate and high prevalence of gastric premalignant lesions. It will utilize biological specimens and epidemiological and histopathological data collected at the baseline examination from the 2200 participants. Genomic DNA will be isolated from these specimens and tested for the polymorphic genes listed above. The specific aim of the proposed study is to evaluate whether those genotypes or alleles of the polymorphic genes which lead to greater responses to HP infection are associated with increased risk of high-grade gastric precancerous lesions. Secondary aims include to examine histopathological correlates of these polymorphisms and to determine whether selected environmental factors modify the above associations.

描述（由申请人提供）：拟议研究的长期目标是为开发针对感染/炎症相关癌症的有效一级预防策略提供科学依据。越来越多的证据表明，各种感染因子在人类癌症的发病机制中发挥作用。据估计，1990年全世界癌症发病率的15.6%可归因于这些传染性病原体，共计145万例。幽门螺杆菌（HP）在各种传染性病原体中排名第一，约占世界新发癌症病例的5%。从公共卫生的角度来看，这些癌症很重要，因为它们可能通过抗生素治疗或疫苗接种来预防。虽然HP感染在胃癌高风险人群中非常常见（80- 90%），但已知感染HP的人群中只有非常小的一部分实际上发展为癌症，这表明除了环境辅助因素外，遗传成分在HP相关致癌作用中也起作用。该建议将特别关注两组多态性基因，即HP脂多糖（LPS）的受体，其是一种细胞壁组分，其引起立即的促炎反应，（1）CD 14（C-260 T），（2）TRL 4（A896 G）和（3）NOD 2（3020 insC）;和所得细胞因子，（4）IL-8（T-251 A），（5）MCP 1（G-2518 A），（6）IL-1 β（T-31 C）和（7）TNF-α（G-308 A）。这些多态性基因是已知的功能，并已被假定为修改宿主对HP感染的反应。拟议的研究将被设计为委内瑞拉胃癌化疗预防试验的衍生研究，利用研究人群的独特特征，即，HP感染率极高（95%），胃癌前病变患病率高。它将利用在基线检查时从2200名参与者中收集的生物标本以及流行病学和组织病理学数据。将从这些标本中分离基因组DNA，并检测上述多态性基因。本研究的具体目的是评估导致对HP感染更大反应的多态性基因的基因型或等位基因是否与高级别胃癌前病变的风险增加相关。次要目的包括检查这些多态性的组织病理学相关性，并确定是否选定的环境因素修改上述协会。

项目成果

TAS2R38 polymorphisms, Helicobacter pylori infection and susceptibility to gastric cancer and premalignant gastric lesions.

• DOI: 10.1097/cej.0000000000000722
• 发表时间: 2022-09-01
• 期刊: European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP)
• 作者: Giaccherini M;Rizzato C;Gentiluomo M;Lupetti A;Flores-Luna L;Vivas J;Bravo MM;Kasamatsu E;Muñoz N;Canzian F;Kato I;Campa D
• 通讯作者: Campa D

Use of whole genome amplification to rescue DNA from plasma samples.

使用全基因组扩增从血浆样本中拯救 DNA。

• DOI: 10.2144/000112005
• 发表时间: 2005
• 期刊: BioTechniques
• 影响因子: 2.7
• 作者: Lu,Yanhui;Gioia-Patricola,Lydie;Gomez,JorgeVivas;Plummer,Martyn;Franceschi,Silvia;Kato,Ikuko;Canzian,Federico
• 通讯作者: Canzian,Federico

Environmental factors in Helicobacter pylori-related gastric precancerous lesions in Venezuela.

委内瑞拉幽门螺杆菌相关胃癌前病变的环境因素。

• 发表时间: 2004
• 期刊: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
• 作者: Kato,Ikuko;Vivas,Jorge;Plummer,Martyn;Lopez,Gladys;Peraza,Simon;Castro,Dennis;Sanchez,Victor;Cano,Elsa;Andrade,Olga;Garcia,Rita;Franceschi,Silvia;Oliver,Walter;Muñoz,Nubia
• 通讯作者: Muñoz,Nubia

Genetic variation in PSCA and risk of gastric advanced preneoplastic lesions and cancer in relation to Helicobacter pylori infection.

• DOI: 10.1371/journal.pone.0073100
• 发表时间: 2013
• 期刊: PloS one
• 影响因子: 3.7
• 作者: Rizzato C;Kato I;Plummer M;Muñoz N;Canzian F
• 通讯作者: Canzian F

Host-bacterial interaction in the development of gastric precancerous lesions in a high risk population for gastric cancer in Venezuela.

委内瑞拉胃癌高危人群胃癌前病变发展中宿主与细菌的相互作用。

• DOI: 10.1002/ijc.21979
• 发表时间: 2006
• 期刊: International journal of cancer
• 影响因子: 6.4
• 作者: Kato,Ikuko;vanDoorn,Leen-Jan;Canzian,Federico;Plummer,Martyn;Franceschi,Silvia;Vivas,Jorge;Lopez,Gladys;Lu,Yanhui;Gioia-Patricola,Lydie;Severson,RichardK;Schwartz,AnnG;Muñoz,Nubia
• 通讯作者: Muñoz,Nubia