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Transforming growth factor (TGF)-beta1 gene common polymorphisms and plasma TGF-beta1 levels in patients with lung cancer

机译:转化生长因子(TGF)-beta1基因常见多态性与血浆TGF-β1水平在肺癌患者中的应用

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摘要

Transforming growth factor (TGF)-b1 is known to regulate many cellularprocesses, including cell proliferation, differentiation, and apoptosis. PlasmaTGF-b1 levels has been shown to be elevated in patients with lung cancer.In this study, we test the association of the polymorphisms at 2 loci, i.e.nucleotide position -509 in the promoter region (C-509T), and nucleotideposition 869 relative to the transcription initiation site (T869C) of theTGF-b1 gene using polymerase chain reaction-restriction fragment lengthpolymorphism (PCR-RFLP) and measure the plasma TGF-b1 levels. TGF-b1genotype and allele frequencies were not significantly different for patientswith lung cancer (n = 102) and controls (nonsmokers, n = 140 or smokers,n = 116). The odds ratio of the TGF-b1 C allele at nucleotide position 869was 0.51 (95% confidence interval 0.25 to 1.06; P = 0.0827) for patients andnonsmoking controls and 0.49 (95% confidence interval 0.23 to 1.03; P =0.0702) for patients and smoking controls in a dominant model (TC + CCversus TT), close to reach significant level. The patients group showedsignificant higher plasma TGF-b1 levels across different genotypes (1852 ±123 pg/ml vs. 3422 ± 158 pg/ml for nonsmoking controls and patientsrespectively). There was no difference in plasma TGF-b1 levels betweensmoking controls and patients. Our results suggest that TGF-b1polymorphisms do not play a role in the pathogenesis of lung cancer, eventhough there remains the possibility of a lower incidence of lung cancer forpolymorphism at nucleotide position 869, which need further investigation.(Supported by a University of Hong Kong, URC/CRCG Research Grant.)
机译:已知转化生长因子(TGF)-b1调节许多细胞过程,包括细胞增殖,分化和凋亡。血浆TGF-b1水平已显示在肺癌患者中升高。在这项研究中,我们测试了2个基因座的多态性的关联,即启动子区域中的核苷酸位置-509(C-509T)和相对的核苷酸位置869用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测TGF-b1基因的转录起始位点(T869C)并测量血浆TGF-b1水平。肺癌患者(n = 102)和对照组(非吸烟者,n = 140或吸烟者,n = 116)的TGF-b1基因型和等位基因频率无明显差异。对于患者和非吸烟对照,TGF-b1 C等位基因在核苷酸位置869的比值比为0.51(95%置信区间0.25至1.06; P = 0.0827),对于患者和非吸烟者,分别为0.49(95%置信区间0.23至1.03; P = 0.0702)。占主导地位的模型(TC + CCversus TT)中的吸烟控制已接近达到显着水平。患者组显示不同基因型的血浆TGF-b1显着较高(非吸烟对照组和患者分别为1852±123 pg / ml与3422±158 pg / ml)。吸烟对照与患者之间血浆TGF-b1水平无差异。我们的结果表明,TGF-b1多态性在肺癌的发病机制中不起作用,尽管仍有可能降低核苷酸869位的肺癌多态性的发生率,这有待进一步研究。(香港大学支持,URC / CRCG研究补助金。)

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