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Association of TNFAIP8 gene polymorphisms with endometrial cancer in northern Chinese women
Tumor necrosis factor-a-induced protein 8 (TNFAIP8) presented a elevated expression in endometrial cancer (EC). However, the relationship of TNFAIP8 gene polymorphisms with EC risk remains unclear. This case-control study aimed to investigate the effect of single nucleotide polymorphisms (SNPs) in T...
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Published in: | Cancer cell international 2019-04, Vol.19 (1), p.105-105, Article 105 |
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description | Tumor necrosis factor-a-induced protein 8 (TNFAIP8) presented a elevated expression in endometrial cancer (EC). However, the relationship of TNFAIP8 gene polymorphisms with EC risk remains unclear. This case-control study aimed to investigate the effect of single nucleotide polymorphisms (SNPs) in TNFAIP8 on northern Chinese women with EC.
SNP rs11064, rs1045241, and rs1045242 in TNFAIP8 were successfully genotyped in 248 cancer-free controls and 226 ECs by SNaPshot method, respectively. Logistic regression was performed to assess relationship of SNPs with EC risk. The relationships of SNPs with clinicopathological variables were evaluated by Chi-square test or Student's t-test or Fisher's text.
The minor alleles of rs11064 in TNFAIP8 were strongly associated with EC risk, with adjust odds ratio (OR) of 1.719 (95% CI 1.180-2.506, P = 0.005). The minor allele of rs1045242 in the TNFAIP8 gene was strongly associated with with EC risk (adjust OR: 1.636, 95% CI 1.107-2.417, P = 0.014). rs11064 SNPs correlated with TNFAIP8 protein expression in EC (P = 0.015). For rs1045242, patients with AG + GG presented higher TNFAIP8 protein expression than that with AA (P = 0.020). It also showed that SNP rs11064 was associated with advanced FIGO stage (P = 0.001), deep myometrial invasion (P = 0.047), and lymph node metastasis (P = 0.048) under the codominant model in ECs.
SNP rs11064 in TNFAIP8 increased EC risk and significantly related with its protein expression in northern Chinese women. |
doi_str_mv | 10.1186/s12935-019-0827-9 |
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SNP rs11064, rs1045241, and rs1045242 in TNFAIP8 were successfully genotyped in 248 cancer-free controls and 226 ECs by SNaPshot method, respectively. Logistic regression was performed to assess relationship of SNPs with EC risk. The relationships of SNPs with clinicopathological variables were evaluated by Chi-square test or Student's t-test or Fisher's text.
The minor alleles of rs11064 in TNFAIP8 were strongly associated with EC risk, with adjust odds ratio (OR) of 1.719 (95% CI 1.180-2.506, P = 0.005). The minor allele of rs1045242 in the TNFAIP8 gene was strongly associated with with EC risk (adjust OR: 1.636, 95% CI 1.107-2.417, P = 0.014). rs11064 SNPs correlated with TNFAIP8 protein expression in EC (P = 0.015). For rs1045242, patients with AG + GG presented higher TNFAIP8 protein expression than that with AA (P = 0.020). It also showed that SNP rs11064 was associated with advanced FIGO stage (P = 0.001), deep myometrial invasion (P = 0.047), and lymph node metastasis (P = 0.048) under the codominant model in ECs.
SNP rs11064 in TNFAIP8 increased EC risk and significantly related with its protein expression in northern Chinese women.</description><identifier>ISSN: 1475-2867</identifier><identifier>EISSN: 1475-2867</identifier><identifier>DOI: 10.1186/s12935-019-0827-9</identifier><identifier>PMID: 31043860</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Age ; Alleles ; Body mass index ; Breast cancer ; Cancer ; Chemotherapy ; Diabetes ; Endometrial cancer ; Endometrium ; Gene expression ; Genotype & phenotype ; Hypertension ; Immunoglobulins ; Lymph nodes ; Medical prognosis ; Metastases ; Myometrium ; Polymorphism ; Primary Research ; Protein expression ; Proteins ; Single-nucleotide polymorphism ; Susceptibility ; TNFAIP8 ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α</subject><ispartof>Cancer cell international, 2019-04, Vol.19 (1), p.105-105, Article 105</ispartof><rights>2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-42420e8be9bf110910bd0e554e6b2f380b4a85bc547aa805253a34b9aecf7b0c3</citedby><cites>FETCH-LOGICAL-c594t-42420e8be9bf110910bd0e554e6b2f380b4a85bc547aa805253a34b9aecf7b0c3</cites><orcidid>0000-0001-6575-0310</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480735/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2227334057?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31043860$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Tianbo</creatorcontrib><creatorcontrib>Jiang, Liangliang</creatorcontrib><creatorcontrib>Yu, Libo</creatorcontrib><creatorcontrib>Ge, Tingting</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Gao, Hongyu</creatorcontrib><title>Association of TNFAIP8 gene polymorphisms with endometrial cancer in northern Chinese women</title><title>Cancer cell international</title><addtitle>Cancer Cell Int</addtitle><description>Tumor necrosis factor-a-induced protein 8 (TNFAIP8) presented a elevated expression in endometrial cancer (EC). However, the relationship of TNFAIP8 gene polymorphisms with EC risk remains unclear. This case-control study aimed to investigate the effect of single nucleotide polymorphisms (SNPs) in TNFAIP8 on northern Chinese women with EC.
SNP rs11064, rs1045241, and rs1045242 in TNFAIP8 were successfully genotyped in 248 cancer-free controls and 226 ECs by SNaPshot method, respectively. Logistic regression was performed to assess relationship of SNPs with EC risk. The relationships of SNPs with clinicopathological variables were evaluated by Chi-square test or Student's t-test or Fisher's text.
The minor alleles of rs11064 in TNFAIP8 were strongly associated with EC risk, with adjust odds ratio (OR) of 1.719 (95% CI 1.180-2.506, P = 0.005). The minor allele of rs1045242 in the TNFAIP8 gene was strongly associated with with EC risk (adjust OR: 1.636, 95% CI 1.107-2.417, P = 0.014). rs11064 SNPs correlated with TNFAIP8 protein expression in EC (P = 0.015). For rs1045242, patients with AG + GG presented higher TNFAIP8 protein expression than that with AA (P = 0.020). It also showed that SNP rs11064 was associated with advanced FIGO stage (P = 0.001), deep myometrial invasion (P = 0.047), and lymph node metastasis (P = 0.048) under the codominant model in ECs.
SNP rs11064 in TNFAIP8 increased EC risk and significantly related with its protein expression in northern Chinese women.</description><subject>Age</subject><subject>Alleles</subject><subject>Body mass index</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Diabetes</subject><subject>Endometrial cancer</subject><subject>Endometrium</subject><subject>Gene expression</subject><subject>Genotype & phenotype</subject><subject>Hypertension</subject><subject>Immunoglobulins</subject><subject>Lymph nodes</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Myometrium</subject><subject>Polymorphism</subject><subject>Primary Research</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Single-nucleotide polymorphism</subject><subject>Susceptibility</subject><subject>TNFAIP8</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><issn>1475-2867</issn><issn>1475-2867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1v1DAQhiMEoqXwA7ggS1y4BMZfsX1BWq0orFQBh3LiYDnOZONVYi92lqr_nixbqpaTR_Y7z4xn3qp6TeE9pbr5UCgzXNZATQ2aqdo8qc6pULJmulFPH8Rn1YtSdgBU6QaeV2ecguBLeF79XJWSfHBzSJGknlx_vVxtvmuyxYhkn8bbKeX9EMpUyE2YB4KxSxPOObiReBc9ZhIiiSnPA-ZI1kOIWJDcLKL4snrWu7Hgq7vzovpx-el6_aW--vZ5s15d1V4aMdeCCQaoWzRtTykYCm0HKKXApmU919AKp2XrpVDOaZBMcsdFaxz6XrXg-UW1OXG75HZ2n8Pk8q1NLti_Fylvrctz8CPalusOwXSKUycAmAHvGt8hdYzqjquF9fHE2h_aCTuPcc5ufAR9_BLDYLfpt22EBsXlAnh3B8jp1wHLbKdQPI6ji5gOxbKlkDGqgWOtt_9Jd-mQ4zKqRcUU5wLkUUVPKp9TKRn7-2Yo2KMN7MkGdrGBPdrAmiXnzcNf3Gf82zv_A7HFrg4</recordid><startdate>20190423</startdate><enddate>20190423</enddate><creator>Liu, Tianbo</creator><creator>Jiang, Liangliang</creator><creator>Yu, Libo</creator><creator>Ge, Tingting</creator><creator>Wang, Jing</creator><creator>Gao, Hongyu</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6575-0310</orcidid></search><sort><creationdate>20190423</creationdate><title>Association of TNFAIP8 gene polymorphisms with endometrial cancer in northern Chinese women</title><author>Liu, Tianbo ; Jiang, Liangliang ; Yu, Libo ; Ge, Tingting ; Wang, Jing ; Gao, Hongyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-42420e8be9bf110910bd0e554e6b2f380b4a85bc547aa805253a34b9aecf7b0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Age</topic><topic>Alleles</topic><topic>Body mass index</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Diabetes</topic><topic>Endometrial cancer</topic><topic>Endometrium</topic><topic>Gene expression</topic><topic>Genotype & phenotype</topic><topic>Hypertension</topic><topic>Immunoglobulins</topic><topic>Lymph nodes</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Myometrium</topic><topic>Polymorphism</topic><topic>Primary Research</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Single-nucleotide polymorphism</topic><topic>Susceptibility</topic><topic>TNFAIP8</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Tianbo</creatorcontrib><creatorcontrib>Jiang, Liangliang</creatorcontrib><creatorcontrib>Yu, Libo</creatorcontrib><creatorcontrib>Ge, Tingting</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Gao, Hongyu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cancer cell international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Tianbo</au><au>Jiang, Liangliang</au><au>Yu, Libo</au><au>Ge, Tingting</au><au>Wang, Jing</au><au>Gao, Hongyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of TNFAIP8 gene polymorphisms with endometrial cancer in northern Chinese women</atitle><jtitle>Cancer cell international</jtitle><addtitle>Cancer Cell Int</addtitle><date>2019-04-23</date><risdate>2019</risdate><volume>19</volume><issue>1</issue><spage>105</spage><epage>105</epage><pages>105-105</pages><artnum>105</artnum><issn>1475-2867</issn><eissn>1475-2867</eissn><abstract>Tumor necrosis factor-a-induced protein 8 (TNFAIP8) presented a elevated expression in endometrial cancer (EC). However, the relationship of TNFAIP8 gene polymorphisms with EC risk remains unclear. This case-control study aimed to investigate the effect of single nucleotide polymorphisms (SNPs) in TNFAIP8 on northern Chinese women with EC.
SNP rs11064, rs1045241, and rs1045242 in TNFAIP8 were successfully genotyped in 248 cancer-free controls and 226 ECs by SNaPshot method, respectively. Logistic regression was performed to assess relationship of SNPs with EC risk. The relationships of SNPs with clinicopathological variables were evaluated by Chi-square test or Student's t-test or Fisher's text.
The minor alleles of rs11064 in TNFAIP8 were strongly associated with EC risk, with adjust odds ratio (OR) of 1.719 (95% CI 1.180-2.506, P = 0.005). The minor allele of rs1045242 in the TNFAIP8 gene was strongly associated with with EC risk (adjust OR: 1.636, 95% CI 1.107-2.417, P = 0.014). rs11064 SNPs correlated with TNFAIP8 protein expression in EC (P = 0.015). For rs1045242, patients with AG + GG presented higher TNFAIP8 protein expression than that with AA (P = 0.020). It also showed that SNP rs11064 was associated with advanced FIGO stage (P = 0.001), deep myometrial invasion (P = 0.047), and lymph node metastasis (P = 0.048) under the codominant model in ECs.
SNP rs11064 in TNFAIP8 increased EC risk and significantly related with its protein expression in northern Chinese women.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>31043860</pmid><doi>10.1186/s12935-019-0827-9</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6575-0310</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Alleles Body mass index Breast cancer Cancer Chemotherapy Diabetes Endometrial cancer Endometrium Gene expression Genotype & phenotype Hypertension Immunoglobulins Lymph nodes Medical prognosis Metastases Myometrium Polymorphism Primary Research Protein expression Proteins Single-nucleotide polymorphism Susceptibility TNFAIP8 Tumor necrosis factor-TNF Tumor necrosis factor-α |
title | Association of TNFAIP8 gene polymorphisms with endometrial cancer in northern Chinese women |
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