Document Type
Article
Publication Date
3-2014
Abstract
AIM: Elevated levels of sterol regulatory element-binding protein-1 (SREBP-1) have been found in endometrial cancer (EC), suggesting that it is essential to the development of EC. Obesity and diabetes have been established as known risk factors of EC, while SREBF-1 gene polymorphisms have also been found to be associated with obesity and type II diabetes. Therefore, we hypothesize that single nucleotide polymorphism (SNP) in SREBF-1 gene may be associated with increased risk of EC.
METHOD: We analyzed the sequence of SREBF-1 in tissue samples from 30 EC cases and 6 benign controls using high throughput method. Based on the primary results, we selected one SNP (rs2297508) as a genetic marker to conduct a hospital-based case-control study with 139 EC cases and 129 benign controls. The samples were examined under the microscope to determine their histopathology prior to the SNP analysis using RT-PCR.
RESULTS: Through sequence analysis, we found 10 SNPs of SREBF-1 associated with EC, including 3 new SNPs. Fourteen percent of EC showed the rs2297508 SNP with C allele, while only 7% had the C allele was present in benign controls (p = 0.027, OR = 1.983). Additionally, the C allele was associated with cancer differentiation (p
CONCLUSION: Our study indicates that SNP (rs2297508) of SREBF-1 may serve as a genetic predisposition factor for the development of EC and screening of such genetic marker may be helpful in its early detection.
Recommended Citation
Qiu, Chun-Ping; Lv, Qing-Tao; Dongol, Samina; Wang, Chenguang; and Jiang, Jie, "Single nucleotide polymorphism of SREBF-1 gene associated with an increased risk of endometrial cancer in Chinese women." (2014). Department of Cancer Biology Faculty Papers. Paper 63.
https://jdc.jefferson.edu/cbfp/63
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
24614076
Comments
This article is the final published version in PLoS ONE
Volume 9, Issue 3, March 2014, Article number e90491.
The published version is available at DOI: 10.1371/journal.pone.0090491
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