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Association between SNPs in Long Non-coding RNAs and the Risk of Female Breast Cancer in a Chinese Population
Long non-coding RNAs (LncRNAs) have been reported to be involved in tumorigenesis and tumor progression. Single nucleotide polymorphisms (SNPs) in the lncRNAs also play a vital role in carcinogenesis. The aim of this study was to assess the relationships between the four selected tagSNPs (rs944289,...
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Published in: | Journal of Cancer 2017-01, Vol.8 (7), p.1162-1169 |
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creator | Xu, Tao Hu, Xiu-Xiu Liu, Xiang-Xiang Wang, Han-Jin Lin, Kang Pan, Yu-Qin Sun, Hui-Ling Peng, Hong-Xin Chen, Xiao-Xiang Wang, Shu-Kui He, Bang-Shun |
description | Long non-coding RNAs (LncRNAs) have been reported to be involved in tumorigenesis and tumor progression. Single nucleotide polymorphisms (SNPs) in the lncRNAs also play a vital role in carcinogenesis. The aim of this study was to assess the relationships between the four selected tagSNPs (rs944289, rs3787016, rs1456315, rs7463708) in the lncRNAs and the risk of female breast cancer in a Chinese population. A case-control study was carried out involving in a total of 439 breast cancer patients and 439 age-matched healthy controls. The genotyping was performed with Sequenom MassARRAY and the expression of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor-2 (HER-2) in tumor tissues was measured by the immunohistochemistry (IHC) assay. We found that rs3787016 TT genotype (adjusted odds ratio (OR) = 1.62, 95% confidence interval (CI) = 1.09-2.41,
= 0.018) was associated with an increased risk of female breast cancer, especially among the patients with premenopausal status (adjusted OR = 2.55, 95% CI = 1.30-4.97,
= 0.006). Moreover, a statistically significant increased risk of the rs3787016 TT genotype was observed among the patients with advanced tumor stage (Ⅲ and Ⅳ), poor histological grade (G3-G4), positive lymph node involvement, positive expression of ER and PR and negative expression of HER-2; rs7463708 GT and GT/GG genotype were associated with decreased risk of breast cancer in the subgroup of patients with postmenopausal status (GT versus (
) TT: adjusted OR = 0.67, 95% CI = 0.46-0.99,
= 0.043; GT/GG
. TT: adjusted OR = 0.68, 95% CI = 0.47-0.98,
= 0.041) and tumor late-stage (GT
TT: adjusted OR = 0.65, 95% CI = 0.43-0.97,
= 0.037; GT/GG
TT: adjusted OR = 0.65, 95% CI = 0.44-0.96,
= 0.029). In short, rs3787016 TT genotype was associated with increased breast cancer risk and clinicopathologic features of the tumor, especially among premenopausal women. |
doi_str_mv | 10.7150/jca.18055 |
format | article |
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= 0.018) was associated with an increased risk of female breast cancer, especially among the patients with premenopausal status (adjusted OR = 2.55, 95% CI = 1.30-4.97,
= 0.006). Moreover, a statistically significant increased risk of the rs3787016 TT genotype was observed among the patients with advanced tumor stage (Ⅲ and Ⅳ), poor histological grade (G3-G4), positive lymph node involvement, positive expression of ER and PR and negative expression of HER-2; rs7463708 GT and GT/GG genotype were associated with decreased risk of breast cancer in the subgroup of patients with postmenopausal status (GT versus (
) TT: adjusted OR = 0.67, 95% CI = 0.46-0.99,
= 0.043; GT/GG
. TT: adjusted OR = 0.68, 95% CI = 0.47-0.98,
= 0.041) and tumor late-stage (GT
TT: adjusted OR = 0.65, 95% CI = 0.43-0.97,
= 0.037; GT/GG
TT: adjusted OR = 0.65, 95% CI = 0.44-0.96,
= 0.029). In short, rs3787016 TT genotype was associated with increased breast cancer risk and clinicopathologic features of the tumor, especially among premenopausal women.</description><identifier>ISSN: 1837-9664</identifier><identifier>EISSN: 1837-9664</identifier><identifier>DOI: 10.7150/jca.18055</identifier><identifier>PMID: 28607590</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher</publisher><subject>Research Paper</subject><ispartof>Journal of Cancer, 2017-01, Vol.8 (7), p.1162-1169</ispartof><rights>Ivyspring International Publisher 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-267b3bf09295ad40221ccb1c5fb73805a804d9cf749ccda4383d9c0a444cee243</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463430/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463430/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28607590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Tao</creatorcontrib><creatorcontrib>Hu, Xiu-Xiu</creatorcontrib><creatorcontrib>Liu, Xiang-Xiang</creatorcontrib><creatorcontrib>Wang, Han-Jin</creatorcontrib><creatorcontrib>Lin, Kang</creatorcontrib><creatorcontrib>Pan, Yu-Qin</creatorcontrib><creatorcontrib>Sun, Hui-Ling</creatorcontrib><creatorcontrib>Peng, Hong-Xin</creatorcontrib><creatorcontrib>Chen, Xiao-Xiang</creatorcontrib><creatorcontrib>Wang, Shu-Kui</creatorcontrib><creatorcontrib>He, Bang-Shun</creatorcontrib><title>Association between SNPs in Long Non-coding RNAs and the Risk of Female Breast Cancer in a Chinese Population</title><title>Journal of Cancer</title><addtitle>J Cancer</addtitle><description>Long non-coding RNAs (LncRNAs) have been reported to be involved in tumorigenesis and tumor progression. Single nucleotide polymorphisms (SNPs) in the lncRNAs also play a vital role in carcinogenesis. The aim of this study was to assess the relationships between the four selected tagSNPs (rs944289, rs3787016, rs1456315, rs7463708) in the lncRNAs and the risk of female breast cancer in a Chinese population. A case-control study was carried out involving in a total of 439 breast cancer patients and 439 age-matched healthy controls. The genotyping was performed with Sequenom MassARRAY and the expression of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor-2 (HER-2) in tumor tissues was measured by the immunohistochemistry (IHC) assay. We found that rs3787016 TT genotype (adjusted odds ratio (OR) = 1.62, 95% confidence interval (CI) = 1.09-2.41,
= 0.018) was associated with an increased risk of female breast cancer, especially among the patients with premenopausal status (adjusted OR = 2.55, 95% CI = 1.30-4.97,
= 0.006). Moreover, a statistically significant increased risk of the rs3787016 TT genotype was observed among the patients with advanced tumor stage (Ⅲ and Ⅳ), poor histological grade (G3-G4), positive lymph node involvement, positive expression of ER and PR and negative expression of HER-2; rs7463708 GT and GT/GG genotype were associated with decreased risk of breast cancer in the subgroup of patients with postmenopausal status (GT versus (
) TT: adjusted OR = 0.67, 95% CI = 0.46-0.99,
= 0.043; GT/GG
. TT: adjusted OR = 0.68, 95% CI = 0.47-0.98,
= 0.041) and tumor late-stage (GT
TT: adjusted OR = 0.65, 95% CI = 0.43-0.97,
= 0.037; GT/GG
TT: adjusted OR = 0.65, 95% CI = 0.44-0.96,
= 0.029). In short, rs3787016 TT genotype was associated with increased breast cancer risk and clinicopathologic features of the tumor, especially among premenopausal women.</description><subject>Research Paper</subject><issn>1837-9664</issn><issn>1837-9664</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVUU1PwzAMjRCITWMH_gDKEQ4dSZN-XZBGxQBpGmjAOUpTd8tok9F0IP492YAJfLEtP79n6yF0SskooRG5XCk5oimJogPUpylLgiyO-eGfuoeGzq2ID5aFCWfHqBemMUmijPRRM3bOKi07bQ0uoPsAMPhp9uiwNnhqzQLPrAmULbUv57Oxw9KUuFsCnmv3im2FJ9DIGvB1C9J1OJdGQbtdljhfagMO8KNdb-qdwgk6qmTtYPiTB-hlcvOc3wXTh9v7fDwNFEuiLgjjpGBFRbIwi2TJSRhSpQqqoqpImH9VpoSXmaoSnilVSs5S5lsiOecKIORsgK6-edebooFSgelaWYt1qxvZfgortfg_MXopFvZdRDxmnBFPcP5D0Nq3DbhONNopqGtpwG6coJk_jqYhZR568Q1VrXWuhWovQ4nYOiS8Q2LnkMee_b1rj_z1g30By8eMDQ</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Xu, Tao</creator><creator>Hu, Xiu-Xiu</creator><creator>Liu, Xiang-Xiang</creator><creator>Wang, Han-Jin</creator><creator>Lin, Kang</creator><creator>Pan, Yu-Qin</creator><creator>Sun, Hui-Ling</creator><creator>Peng, Hong-Xin</creator><creator>Chen, Xiao-Xiang</creator><creator>Wang, Shu-Kui</creator><creator>He, Bang-Shun</creator><general>Ivyspring International Publisher</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170101</creationdate><title>Association between SNPs in Long Non-coding RNAs and the Risk of Female Breast Cancer in a Chinese Population</title><author>Xu, Tao ; Hu, Xiu-Xiu ; Liu, Xiang-Xiang ; Wang, Han-Jin ; Lin, Kang ; Pan, Yu-Qin ; Sun, Hui-Ling ; Peng, Hong-Xin ; Chen, Xiao-Xiang ; Wang, Shu-Kui ; He, Bang-Shun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-267b3bf09295ad40221ccb1c5fb73805a804d9cf749ccda4383d9c0a444cee243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Research Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Tao</creatorcontrib><creatorcontrib>Hu, Xiu-Xiu</creatorcontrib><creatorcontrib>Liu, Xiang-Xiang</creatorcontrib><creatorcontrib>Wang, Han-Jin</creatorcontrib><creatorcontrib>Lin, Kang</creatorcontrib><creatorcontrib>Pan, Yu-Qin</creatorcontrib><creatorcontrib>Sun, Hui-Ling</creatorcontrib><creatorcontrib>Peng, Hong-Xin</creatorcontrib><creatorcontrib>Chen, Xiao-Xiang</creatorcontrib><creatorcontrib>Wang, Shu-Kui</creatorcontrib><creatorcontrib>He, Bang-Shun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Tao</au><au>Hu, Xiu-Xiu</au><au>Liu, Xiang-Xiang</au><au>Wang, Han-Jin</au><au>Lin, Kang</au><au>Pan, Yu-Qin</au><au>Sun, Hui-Ling</au><au>Peng, Hong-Xin</au><au>Chen, Xiao-Xiang</au><au>Wang, Shu-Kui</au><au>He, Bang-Shun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between SNPs in Long Non-coding RNAs and the Risk of Female Breast Cancer in a Chinese Population</atitle><jtitle>Journal of Cancer</jtitle><addtitle>J Cancer</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>8</volume><issue>7</issue><spage>1162</spage><epage>1169</epage><pages>1162-1169</pages><issn>1837-9664</issn><eissn>1837-9664</eissn><abstract>Long non-coding RNAs (LncRNAs) have been reported to be involved in tumorigenesis and tumor progression. Single nucleotide polymorphisms (SNPs) in the lncRNAs also play a vital role in carcinogenesis. The aim of this study was to assess the relationships between the four selected tagSNPs (rs944289, rs3787016, rs1456315, rs7463708) in the lncRNAs and the risk of female breast cancer in a Chinese population. A case-control study was carried out involving in a total of 439 breast cancer patients and 439 age-matched healthy controls. The genotyping was performed with Sequenom MassARRAY and the expression of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor-2 (HER-2) in tumor tissues was measured by the immunohistochemistry (IHC) assay. We found that rs3787016 TT genotype (adjusted odds ratio (OR) = 1.62, 95% confidence interval (CI) = 1.09-2.41,
= 0.018) was associated with an increased risk of female breast cancer, especially among the patients with premenopausal status (adjusted OR = 2.55, 95% CI = 1.30-4.97,
= 0.006). Moreover, a statistically significant increased risk of the rs3787016 TT genotype was observed among the patients with advanced tumor stage (Ⅲ and Ⅳ), poor histological grade (G3-G4), positive lymph node involvement, positive expression of ER and PR and negative expression of HER-2; rs7463708 GT and GT/GG genotype were associated with decreased risk of breast cancer in the subgroup of patients with postmenopausal status (GT versus (
) TT: adjusted OR = 0.67, 95% CI = 0.46-0.99,
= 0.043; GT/GG
. TT: adjusted OR = 0.68, 95% CI = 0.47-0.98,
= 0.041) and tumor late-stage (GT
TT: adjusted OR = 0.65, 95% CI = 0.43-0.97,
= 0.037; GT/GG
TT: adjusted OR = 0.65, 95% CI = 0.44-0.96,
= 0.029). In short, rs3787016 TT genotype was associated with increased breast cancer risk and clinicopathologic features of the tumor, especially among premenopausal women.</abstract><cop>Australia</cop><pub>Ivyspring International Publisher</pub><pmid>28607590</pmid><doi>10.7150/jca.18055</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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title | Association between SNPs in Long Non-coding RNAs and the Risk of Female Breast Cancer in a Chinese Population |
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