scholarly journals Estrogen-metabolizing gene polymorphisms in the assessment of breast carcinoma risk and fibroadenoma risk in Caucasian women

Cancer ◽  
2004 ◽  
Vol 101 (2) ◽  
pp. 264-269 ◽  
Author(s):  
Lukas A. Hefler ◽  
Clemens B. Tempfer ◽  
Christoph Grimm ◽  
Antje Lebrecht ◽  
Eva Ulbrich ◽  
...  
2012 ◽  
Vol 138 (9) ◽  
pp. 1449-1462 ◽  
Author(s):  
Huizhe Wu ◽  
Hui Kang ◽  
Yong Liu ◽  
Weiwei Tong ◽  
Duo Liu ◽  
...  

2005 ◽  
Vol 20 (5) ◽  
pp. 1422-1427 ◽  
Author(s):  
L.A. Hefler ◽  
C. Grimm ◽  
G. Heinze ◽  
C. Schneeberger ◽  
M.W. Mueller ◽  
...  

2020 ◽  
Vol 48 (8) ◽  
pp. 030006052094342
Author(s):  
Cunqing Kong ◽  
Miao Chen ◽  
Xiaohui Fan ◽  
Xingcai Chen

Background Interleukin-12 (IL-12) is considered to be a risk factor for cancer; however, its role in hepatocellular carcinoma (HCC) remains unknown. This study aimed to explore the impacts of the IL-12 rs3212227 and rs568408 gene polymorphisms on HCC. Methods We searched PubMed, Embase, Web of Science, and Chinese Knowledge Infrastructure databases for studies on the associations between HCC and IL-12 rs568408 and rs3212227 polymorphisms published prior to 1 May 2020. The effects of the polymorphisms on HCC susceptibility were presented as odds ratios (ORs) and associated 95% confidence intervals. Results Seven studies were ultimately included, including 2375 cases and 3445 controls. The rs3212227 polymorphism was significantly associated with the risk of HCC in both the dominant model (CC+AC vs. AA, OR=1.22) and the allele model (C vs. A, OR=1.12). Combined analysis of rs568408 yielded a significant relative risk for HCC in the dominant (AA+AG vs. GG, OR=1.13), recessive (AA vs. AG+GG, OR=1.72), allele (A vs. G, OR=1.29), heterozygote (AG vs. GG, OR=1.27), and homozygote models (AA vs. GG, OR 1.17). Conclusion The IL-12 rs3212227 and rs568408 gene polymorphisms are associated with an increased risk of HCC.


BMC Cancer ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Christoph Grimm ◽  
Eva Kantelhardt ◽  
Georg Heinze ◽  
Stephan Polterauer ◽  
Robert Zeillinger ◽  
...  

Author(s):  
Michał Ciebiera ◽  
Małgorzata Wrzosek ◽  
Cezary Wojtyła ◽  
Kornelia Zaręba ◽  
Grażyna Nowicka ◽  
...  

Medicina ◽  
2019 ◽  
Vol 55 (8) ◽  
pp. 435
Author(s):  
Biljana Dragicevic ◽  
Sonja Suvakov ◽  
Djurdja Jerotic ◽  
Zorica Reljic ◽  
Ljubica Djukanovic ◽  
...  

Background: Experimental data show that superoxide dismutase 2 (SOD2) is involved in ochratoxin (OTA)-induced nephrotoxicity, whereas clinical data indicate the role of SOD2 rs4880 or glutathione peroxidase 1 (GPX1) rs1050450 polymorphisms in end-stage renal disease and urothelial carcinoma risk, known to be the major complications of Balkan endemic nephropathy (BEN). Therefore, we hypothesized that SOD2 and GPX1 gene polymorphisms would influence the risk of BEN and its associated tumors. Materials and Methods: The study was conducted in 207 BEN patients and 86 controls from endemic areas. Results: Individuals with both copies of variant SOD2 allele, known for lower mitochondrial antioxidant protection, are at a significantly higher BEN risk (OR = 2.6, p = 0.021). No association was observed between GPX1 gene polymorphism and BEN risk. Combining SOD2 and GPX1 genotypes did not alter the risk of BEN development. Regarding the risk of urothelial tumors in BEN patients, none of the polymorphisms studied was significantly associated with the risk of these tumors. Conclusions: Polymorphism in SOD2 rs4880 gene affects the risk of BEN development. Hence, SOD2 genotyping could, together with a panel of other enzymes, be used as a biomarker of susceptibility in BEN areas.


Cancer ◽  
1999 ◽  
Vol 85 (11) ◽  
pp. 2400-2409 ◽  
Author(s):  
Catherine S. Berkey ◽  
A. Lindsay Frazier ◽  
Jane D. Gardner ◽  
Graham A. Colditz

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