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Inherited alterations of TGF beta signaling components in Appalachian cervical cancers

机译:Appalachian宫颈癌中TGFβ信号传导组分的遗传改变

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Purpose This study examined targeted genomic variants of transforming growth factor beta (TGFB) signaling in Appalachian women. Appalachian women with cervical cancer were compared to healthy Appalachian counterparts to determine whether these polymorphic alleles were over-represented within this high-risk cancer population, and whether lifestyle or environmental factors modified the aggregate genetic risk in these Appalachian women. Methods Appalachian women's survey data and blood samples from the Community Awareness, Resources, and Education (CARE) CARE I and CARE II studies (n = 163 invasive cervical cancer cases, 842 controls) were used to assess gene-environment interactions and cancer risk. Polymorphic allele frequencies and socio-behavioral demographic measurements were compared using t tests and chi(2) tests. Multivariable logistic regression was used to evaluate interaction effects between genomic variance and demographic, behavioral, and environmental characteristics. Results Several alleles demonstrated significant interaction with smoking (TP53 rs1042522, TGFB1 rs1800469), alcohol consumption (NQO1 rs1800566), and sexual intercourse before the age of 18 (TGFBR1 rs11466445, TGFBR1 rs7034462, TGFBR1 rs11568785). Interestingly, we noted a significant interaction between "Appalachian self-identity" variables and NQO1 rs1800566. Multivariable logistic regression of cancer status in an over-dominant TGFB1 rs1800469/TGFBR1 rs11568785 model demonstrated a 3.03-fold reduction in cervical cancer odds. Similar decreased odds (2.78-fold) were observed in an over-dominant TGFB1 rs1800469/TGFBR1 rs7034462 model in subjects who had no sexual intercourse before age 18. Conclusions This study reports novel associations between common low-penetrance alleles in the TGFB signaling cascade and modified risk of cervical cancer in Appalachian women. Furthermore, our unexpected findings associating Appalachian identity and NQO1 rs1800566 suggests that the complex environmental exposures that contribute to Appalachian self-identity in Appalachian cervical cancer patients represent an emerging avenue of scientific exploration.
机译:目的本研究检测了在阿巴拉契亚女性中转化生长因子β(TGFB)信号传导的靶向基因组变体。将宫颈癌的阿巴拉契亚女性与健康的阿巴拉契亚对应物进行比较,以确定这些多晶型等位基因是否在这种高危癌症人群中过度代表,以及生活方式或环境因素是否在这些阿巴拉契亚女性中修改了总遗传风险。方法采购Appalachian妇女的调查数据和血液样本来自社区意识,资源和教育(护理)护理I和护理II研究(n = 163次侵袭性宫颈癌病例,842种对照)用于评估基因 - 环境相互作用和癌症风险。使用T测试和CHI(2)测试进行比较多态等位基因频率和社会行为人口统计学测量。多变量逻辑回归用于评估基因组方差和人口统计,行为和环境特征之间的相互作用。结果几个等位基因显示出与吸烟的显着相互作用(TP53 RS1042522,TGFB1 RS1800469),酒精消耗(NQO1 RS1800566)和18岁以前的性交(TGFBR1 RS1146445,TGFBR1 RS7034462,TGFBR1 RS11568785)。有趣的是,我们注意到“Appalachian自我认同”变量和NQO1 RS180066之间的重大互动。过度优势TGFB1 RS1800469 / TGFBR1 rs11568785模型中的多变量逻辑回归癌症状况展示了宫颈癌差异的3.03倍。在18岁之前在没有性交的受试者中观察到类似的赔率(2.78倍)的赔率(2.78倍)。结论本研究报告了TGFB信号传导级联的普通低渗等位基因之间的新联合阿巴拉契亚女性宫颈癌的改良风险。此外,我们的意外发现与阿巴拉契亚身份和NQO1 RS180066相关的意外发现表明,在阿巴拉契亚宫颈癌患者中有助于阿巴拉契亚自我认同的复杂环境暴露代表了科学勘探的新兴大道。

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