Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Abstract 1336: A population-based study of Transforming Growth Factor-Beta1 (TGFB1) polymorphisms and risk of breast cancer.

View through CrossRef
Abstract Transforming growth factor-beta1 (TGFB1) is a multifunctional cytokine that may play an important role in the development and progression of cancer. The results of a number of association studies of TGFB1 polymorphisms and breast cancer risk are inconclusive. This study examined 4 single nucleotide polymorphisms (SNPs) in TGFB1 and risk of breast cancer using data previously collected from a population based case-control study (n=307 cases and 664 controls) of Caucasian women conducted in Northeastern Ontario, Canada. The SNPs (rs8179181, rs8110090, rs1800470 (L10P), rs1800469 (-509C/T)) were selected as either tag SNPs or had been identified as potentially functional in other studies, and were analysed using Taqman genotyping assays. Two of the SNPs were at the 5’ end (rs1800469 (-509C/T), rs1800470) and were in high LD (D’ 0.98); the remaining SNPs (rs8179181, rs8110090) were at the 3’ end and were also in high LD (D’ 0.99). In single-SNP analyses, the variant homozygous genotypes in rs1800470 (CC) and rs8179181 (AA) were significantly protective in the codominant model with Odds Ratios (OR) and 95% Confidence Intervals (95% CIs) of 0.63 (0.40-0.99) and 0.45 (0.21-0.96), while the AG genotype of rs8110090 was significantly associated with increased breast cancer risk with an OR of 1.78 (95% CI 1.14-2.77). Of the seven estimated haplotypes, 3 were significantly protective for breast cancer; when compared to the referent haplotype (see Table). In conclusion, our results suggest that SNPs at both the 3’ and 5’ end of TGFB1 may be associated with risk of breast cancer, and future studies examining additional polymorphisms in these regions would be valuable. Haplotype association with breast cancer risk (n = 969; Global Haplotype Association p-value 0.0021)rs8179181rs8110090rs1800470rs1800469FrequencyOR (95% CI)P-value1GATC0.40281.002GACT0.23870.73 (0.55–0.97)0.033AATC0.17280.67 (0.48–0.93)0.0174GACC0.06710.49 (0.30–0.81)0.00545AACT0.0560.55 (0.30–1.00)0.0526GGTC0.02981.00 (0.48–2.09)0.997GGCT0.02271.82 (0.82–4.06)0.14 Citation Format: Mary A. Bewick, Michael SC Conlon. A population-based study of Transforming Growth Factor-Beta1 (TGFB1) polymorphisms and risk of breast cancer. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 1336. doi:10.1158/1538-7445.AM2013-1336
American Association for Cancer Research (AACR)
Title: Abstract 1336: A population-based study of Transforming Growth Factor-Beta1 (TGFB1) polymorphisms and risk of breast cancer.
Description:
Abstract Transforming growth factor-beta1 (TGFB1) is a multifunctional cytokine that may play an important role in the development and progression of cancer.
The results of a number of association studies of TGFB1 polymorphisms and breast cancer risk are inconclusive.
This study examined 4 single nucleotide polymorphisms (SNPs) in TGFB1 and risk of breast cancer using data previously collected from a population based case-control study (n=307 cases and 664 controls) of Caucasian women conducted in Northeastern Ontario, Canada.
The SNPs (rs8179181, rs8110090, rs1800470 (L10P), rs1800469 (-509C/T)) were selected as either tag SNPs or had been identified as potentially functional in other studies, and were analysed using Taqman genotyping assays.
Two of the SNPs were at the 5’ end (rs1800469 (-509C/T), rs1800470) and were in high LD (D’ 0.
98); the remaining SNPs (rs8179181, rs8110090) were at the 3’ end and were also in high LD (D’ 0.
99).
In single-SNP analyses, the variant homozygous genotypes in rs1800470 (CC) and rs8179181 (AA) were significantly protective in the codominant model with Odds Ratios (OR) and 95% Confidence Intervals (95% CIs) of 0.
63 (0.
40-0.
99) and 0.
45 (0.
21-0.
96), while the AG genotype of rs8110090 was significantly associated with increased breast cancer risk with an OR of 1.
78 (95% CI 1.
14-2.
77).
Of the seven estimated haplotypes, 3 were significantly protective for breast cancer; when compared to the referent haplotype (see Table).
In conclusion, our results suggest that SNPs at both the 3’ and 5’ end of TGFB1 may be associated with risk of breast cancer, and future studies examining additional polymorphisms in these regions would be valuable.
Haplotype association with breast cancer risk (n = 969; Global Haplotype Association p-value 0.
0021)rs8179181rs8110090rs1800470rs1800469FrequencyOR (95% CI)P-value1GATC0.
40281.
002GACT0.
23870.
73 (0.
55–0.
97)0.
033AATC0.
17280.
67 (0.
48–0.
93)0.
0174GACC0.
06710.
49 (0.
30–0.
81)0.
00545AACT0.
0560.
55 (0.
30–1.
00)0.
0526GGTC0.
02981.
00 (0.
48–2.
09)0.
997GGCT0.
02271.
82 (0.
82–4.
06)0.
14 Citation Format: Mary A.
Bewick, Michael SC Conlon.
A population-based study of Transforming Growth Factor-Beta1 (TGFB1) polymorphisms and risk of breast cancer.
[abstract].
In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC.
Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 1336.
doi:10.
1158/1538-7445.
AM2013-1336.

Related Results

Breast Carcinoma within Fibroadenoma: A Systematic Review
Breast Carcinoma within Fibroadenoma: A Systematic Review
Abstract Introduction Fibroadenoma is the most common benign breast lesion; however, it carries a potential risk of malignant transformation. This systematic review provides an ove...
Desmoid-Type Fibromatosis of The Breast: A Case Series
Desmoid-Type Fibromatosis of The Breast: A Case Series
Abstract IntroductionDesmoid-type fibromatosis (DTF), also called aggressive fibromatosis, is a rare, benign, locally aggressive condition. Mammary DTF originates from fibroblasts ...
Effects of TGFB1 and 17 B estradiol on corneal stiffness and thickness
Effects of TGFB1 and 17 B estradiol on corneal stiffness and thickness
Background: Impaired corneal stiffness and transparency are the hallmarks of some of the leading global causes of corneal blindness diseases, such as keratoconus (KCN) which is cha...
Abstract OI-1: OI-1 Decoding breast cancer predisposition genes
Abstract OI-1: OI-1 Decoding breast cancer predisposition genes
Abstract Women with one or more first-degree female relatives with a history of breast cancer have a two-fold increased risk of developing breast cancer. This risk i...
Natural and environmental oestrogens induce TGFB1 synthesis in oviduct cells
Natural and environmental oestrogens induce TGFB1 synthesis in oviduct cells
Abstract Autocrine/paracrine factors generated in response to 17β-oestradiol (E2), within the oviduct, facilitate early embryo development for implantation. Since...
Abstract P3-09-11: A genetically underserved community
Abstract P3-09-11: A genetically underserved community
Abstract It is estimated 5-10% of breast cancer can be attributed to a hereditary predisposition. By knowing a woman's risk for breast cancer, risk reduction strateg...
Spanish Breast Cancer Research Group (GEICAM)
Spanish Breast Cancer Research Group (GEICAM)
This section provides current contact details and a summary of recent or ongoing clinical trials being coordinated by Spanish Breast Cancer Research Group (GEICAM). Clinical trials...

Back to Top