PTEN gene polymorphisms and susceptibility to oral squamous cell carcinoma in a Chinese Han population
The tumor suppressor gene phosphatase and tensin homologue (PTEN) plays a significant role in regulating cell growth, proliferation, and apoptosis. However, there are no data regarding the role of PTEN polymorphisms in the development of oral squamous cell carcinoma (OSCC). A hospital-based case–con...
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description | The tumor suppressor gene phosphatase and tensin homologue (PTEN) plays a significant role in regulating cell growth, proliferation, and apoptosis. However, there are no data regarding the role of PTEN polymorphisms in the development of oral squamous cell carcinoma (OSCC). A hospital-based case–control study was conducted to investigate the potential association between PTEN polymorphisms and the risk of OSCC in a Chinese Han population. The study population comprised 201 patients with OSCC and 199 healthy controls. Seventeen single-nucleotide polymorphisms (SNPs) of PTEN were investigated and genotyped using Sequenom Mass ARRAY and iPLEX-MALDI-TOF technology. The observed genotype frequencies of these polymorphisms were in agreement with Hardy-Weinberg equilibrium in the control group (
P
> 0.05 for all). The heterozygous CT genotype was not associated with significantly increased risk for OSCC (OR = 0.89, 95 % CI = (0.55–1.42),
P
= 0.83), the TT genotype was not associated with increased risk for OSCC (OR = 1.01, 95 % CI = (0.58–1.74),
P
= 0.74) compared to the PTEN SNP rs1234224 homozygous CC genotype. Meanwhile, CT/TT variants were not associated with increased risk for OSCC compared with the CC genotype (OR = 0.93, 95 % CI = 0.60–1.44,
P
= 0.73). The T allele was not associated with significantly increased risk compared to the C allele (OR = 0.99, 95 % CI = 0.72–1.58,
P
= 0.69). Similar associations with the risk of OSCC were observed for the other genotypes of PTEN gene polymorphisms. There were no significant differences in the distribution of the genotype and allele frequencies of polymorphisms of the PTEN gene between the OSCC patients and controls in a Chinese Han population. Further studies are needed to clarify the specific roles of PTEN polymorphisms in the etiology of OSCC. |
doi_str_mv | 10.1007/s13277-015-3804-5 |
format | Article |
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P
> 0.05 for all). The heterozygous CT genotype was not associated with significantly increased risk for OSCC (OR = 0.89, 95 % CI = (0.55–1.42),
P
= 0.83), the TT genotype was not associated with increased risk for OSCC (OR = 1.01, 95 % CI = (0.58–1.74),
P
= 0.74) compared to the PTEN SNP rs1234224 homozygous CC genotype. Meanwhile, CT/TT variants were not associated with increased risk for OSCC compared with the CC genotype (OR = 0.93, 95 % CI = 0.60–1.44,
P
= 0.73). The T allele was not associated with significantly increased risk compared to the C allele (OR = 0.99, 95 % CI = 0.72–1.58,
P
= 0.69). Similar associations with the risk of OSCC were observed for the other genotypes of PTEN gene polymorphisms. There were no significant differences in the distribution of the genotype and allele frequencies of polymorphisms of the PTEN gene between the OSCC patients and controls in a Chinese Han population. Further studies are needed to clarify the specific roles of PTEN polymorphisms in the etiology of OSCC.</description><identifier>ISSN: 1010-4283</identifier><identifier>EISSN: 1423-0380</identifier><identifier>DOI: 10.1007/s13277-015-3804-5</identifier><identifier>PMID: 26232326</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adult ; Aged ; Alleles ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - pathology ; Case-Control Studies ; China ; Female ; Gene Frequency ; Genes ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Middle Aged ; Mouth Neoplasms - genetics ; Mouth Neoplasms - pathology ; Odds Ratio ; Oral cancer ; Original Article ; Polymorphism ; Polymorphism, Single Nucleotide ; PTEN Phosphohydrolase - genetics ; Risk Factors ; Tumors</subject><ispartof>Tumor biology, 2016, Vol.37 (1), p.577-582</ispartof><rights>International Society of Oncology and BioMarkers (ISOBM) 2015</rights><rights>International Society of Oncology and BioMarkers (ISOBM) 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-ef14994f786380407432983e99b11177a1462d9b4854f9d9e030847ed42ab8953</citedby><cites>FETCH-LOGICAL-c372t-ef14994f786380407432983e99b11177a1462d9b4854f9d9e030847ed42ab8953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s13277-015-3804-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s13277-015-3804-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26232326$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Xu-Dong</creatorcontrib><creatorcontrib>Zhao, Su-Feng</creatorcontrib><creatorcontrib>Zhang, Qian</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Wang, Yu-Xin</creatorcontrib><creatorcontrib>Hong, Xiao-Wei</creatorcontrib><creatorcontrib>Hu, Qin-Gang</creatorcontrib><title>PTEN gene polymorphisms and susceptibility to oral squamous cell carcinoma in a Chinese Han population</title><title>Tumor biology</title><addtitle>Tumor Biol</addtitle><addtitle>Tumour Biol</addtitle><description>The tumor suppressor gene phosphatase and tensin homologue (PTEN) plays a significant role in regulating cell growth, proliferation, and apoptosis. However, there are no data regarding the role of PTEN polymorphisms in the development of oral squamous cell carcinoma (OSCC). A hospital-based case–control study was conducted to investigate the potential association between PTEN polymorphisms and the risk of OSCC in a Chinese Han population. The study population comprised 201 patients with OSCC and 199 healthy controls. Seventeen single-nucleotide polymorphisms (SNPs) of PTEN were investigated and genotyped using Sequenom Mass ARRAY and iPLEX-MALDI-TOF technology. The observed genotype frequencies of these polymorphisms were in agreement with Hardy-Weinberg equilibrium in the control group (
P
> 0.05 for all). The heterozygous CT genotype was not associated with significantly increased risk for OSCC (OR = 0.89, 95 % CI = (0.55–1.42),
P
= 0.83), the TT genotype was not associated with increased risk for OSCC (OR = 1.01, 95 % CI = (0.58–1.74),
P
= 0.74) compared to the PTEN SNP rs1234224 homozygous CC genotype. Meanwhile, CT/TT variants were not associated with increased risk for OSCC compared with the CC genotype (OR = 0.93, 95 % CI = 0.60–1.44,
P
= 0.73). The T allele was not associated with significantly increased risk compared to the C allele (OR = 0.99, 95 % CI = 0.72–1.58,
P
= 0.69). Similar associations with the risk of OSCC were observed for the other genotypes of PTEN gene polymorphisms. There were no significant differences in the distribution of the genotype and allele frequencies of polymorphisms of the PTEN gene between the OSCC patients and controls in a Chinese Han population. Further studies are needed to clarify the specific roles of PTEN polymorphisms in the etiology of OSCC.</description><subject>Adult</subject><subject>Aged</subject><subject>Alleles</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Case-Control Studies</subject><subject>China</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genes</subject><subject>Genetic Association Studies</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mouth Neoplasms - genetics</subject><subject>Mouth Neoplasms - pathology</subject><subject>Odds Ratio</subject><subject>Oral cancer</subject><subject>Original Article</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>PTEN Phosphohydrolase - genetics</subject><subject>Risk Factors</subject><subject>Tumors</subject><issn>1010-4283</issn><issn>1423-0380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtPxCAUhYnR6Pj4AW4MiRs3KK-WsjQTX8lEXeia0JbOMGmhQruYfy91RmNMDAsg9-Nw7rkAnBN8TTAWN5EwKgTCJEOswBxle2BGOGUIp-t-OmOCEacFOwLHMa5xAqXMD8ERzSlLK5-B5vXt7hkujTOw9-2m86Ff2dhFqF0N4xgr0w-2tK0dNnDw0Afdwvgx6s6PEVambWGlQ2Wd7zS0Dmo4X1lnooGP2iXFfmz1YL07BQeNbqM52-0n4P3-7m3-iBYvD0_z2wWqmKADMg3hUvJGFPnUEBacUVkwI2VJCBFCE57TWpa8yHgja2kwwwUXpuZUl4XM2Am42ur2wX-MJg6qs3GyqZ1JjhURBZMEZ5gm9PIPuvZjcMndF5XnLKWXKLKlquBjDKZRfbCdDhtFsJqGoLZDUClbNXlWk4mLnfJYdqb-efGdegLoFoip5JYm_Pr6X9VPbP2QJw</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Yang, Xu-Dong</creator><creator>Zhao, Su-Feng</creator><creator>Zhang, Qian</creator><creator>Li, Wei</creator><creator>Wang, Yu-Xin</creator><creator>Hong, Xiao-Wei</creator><creator>Hu, Qin-Gang</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>2016</creationdate><title>PTEN gene polymorphisms and susceptibility to oral squamous cell carcinoma in a Chinese Han population</title><author>Yang, Xu-Dong ; Zhao, Su-Feng ; Zhang, Qian ; Li, Wei ; Wang, Yu-Xin ; Hong, Xiao-Wei ; Hu, Qin-Gang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-ef14994f786380407432983e99b11177a1462d9b4854f9d9e030847ed42ab8953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alleles</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Case-Control Studies</topic><topic>China</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genes</topic><topic>Genetic Association Studies</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mouth Neoplasms - genetics</topic><topic>Mouth Neoplasms - pathology</topic><topic>Odds Ratio</topic><topic>Oral cancer</topic><topic>Original Article</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>PTEN Phosphohydrolase - genetics</topic><topic>Risk Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Xu-Dong</creatorcontrib><creatorcontrib>Zhao, Su-Feng</creatorcontrib><creatorcontrib>Zhang, Qian</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Wang, Yu-Xin</creatorcontrib><creatorcontrib>Hong, Xiao-Wei</creatorcontrib><creatorcontrib>Hu, Qin-Gang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Tumor biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Xu-Dong</au><au>Zhao, Su-Feng</au><au>Zhang, Qian</au><au>Li, Wei</au><au>Wang, Yu-Xin</au><au>Hong, Xiao-Wei</au><au>Hu, Qin-Gang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PTEN gene polymorphisms and susceptibility to oral squamous cell carcinoma in a Chinese Han population</atitle><jtitle>Tumor biology</jtitle><stitle>Tumor Biol</stitle><addtitle>Tumour Biol</addtitle><date>2016</date><risdate>2016</risdate><volume>37</volume><issue>1</issue><spage>577</spage><epage>582</epage><pages>577-582</pages><issn>1010-4283</issn><eissn>1423-0380</eissn><abstract>The tumor suppressor gene phosphatase and tensin homologue (PTEN) plays a significant role in regulating cell growth, proliferation, and apoptosis. However, there are no data regarding the role of PTEN polymorphisms in the development of oral squamous cell carcinoma (OSCC). A hospital-based case–control study was conducted to investigate the potential association between PTEN polymorphisms and the risk of OSCC in a Chinese Han population. The study population comprised 201 patients with OSCC and 199 healthy controls. Seventeen single-nucleotide polymorphisms (SNPs) of PTEN were investigated and genotyped using Sequenom Mass ARRAY and iPLEX-MALDI-TOF technology. The observed genotype frequencies of these polymorphisms were in agreement with Hardy-Weinberg equilibrium in the control group (
P
> 0.05 for all). The heterozygous CT genotype was not associated with significantly increased risk for OSCC (OR = 0.89, 95 % CI = (0.55–1.42),
P
= 0.83), the TT genotype was not associated with increased risk for OSCC (OR = 1.01, 95 % CI = (0.58–1.74),
P
= 0.74) compared to the PTEN SNP rs1234224 homozygous CC genotype. Meanwhile, CT/TT variants were not associated with increased risk for OSCC compared with the CC genotype (OR = 0.93, 95 % CI = 0.60–1.44,
P
= 0.73). The T allele was not associated with significantly increased risk compared to the C allele (OR = 0.99, 95 % CI = 0.72–1.58,
P
= 0.69). Similar associations with the risk of OSCC were observed for the other genotypes of PTEN gene polymorphisms. There were no significant differences in the distribution of the genotype and allele frequencies of polymorphisms of the PTEN gene between the OSCC patients and controls in a Chinese Han population. Further studies are needed to clarify the specific roles of PTEN polymorphisms in the etiology of OSCC.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>26232326</pmid><doi>10.1007/s13277-015-3804-5</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Alleles Biomedical and Life Sciences Biomedicine Cancer Research Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - pathology Case-Control Studies China Female Gene Frequency Genes Genetic Association Studies Genetic Predisposition to Disease Genotype Humans Male Middle Aged Mouth Neoplasms - genetics Mouth Neoplasms - pathology Odds Ratio Oral cancer Original Article Polymorphism Polymorphism, Single Nucleotide PTEN Phosphohydrolase - genetics Risk Factors Tumors |
title | PTEN gene polymorphisms and susceptibility to oral squamous cell carcinoma in a Chinese Han population |
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