Genetic Polymorphisms in Pre-microRNA Genes as Prognostic Markers of Colorectal Cancer
Cumulative data have shown that microRNAs (miRNA) are involved in the etiology and prognosis of colorectal cancer (CRC). Genetic polymorphisms in pre-miRNA genes may influence the biogenesis and functions of their host miRNAs. However, whether these polymorphisms are associated with CRC prognosis re...
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Veröffentlicht in: | Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2012-01, Vol.21 (1), p.217-227 |
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creator | JINLIANG XING SHAOGUI WAN HUSHAN YANG FENG ZHOU FALIN QU BINGSHAN LI MYERS, Ronald E XIAOYING FU PALAZZO, Juan P XIANLI HE ZHINAN CHEN |
description | Cumulative data have shown that microRNAs (miRNA) are involved in the etiology and prognosis of colorectal cancer (CRC). Genetic polymorphisms in pre-miRNA genes may influence the biogenesis and functions of their host miRNAs. However, whether these polymorphisms are associated with CRC prognosis remains unknown.
We analyzed the effects of seven single-nucleotide polymorphisms (SNP) in pre-miRNA genes on the prognosis of a Chinese population with 408 CRC patients with surgically-resected adenocarcinoma.
Two SNPs were identified to be significantly associated with recurrence-free survival and overall survival of the patients. The most significant SNP was rs6505162 in pre-miR-423. Compared with the homozygous wild-type genotype, the variant-containing genotypes of this SNP were significantly associated with both the overall survival (HR = 2.12, 95% CI = 1.34-3.34, P = 0.001) and the recurrence-free survival (HR = 1.59, 95% CI = 1.08-2.36, P = 0.019). Another SNP, rs4919510 in pre-miR-608, was also associated with altered recurrence-free survival (HR = 0.61, 95% CI = 0.41-0.92, P = 0.017). These effects were evident only in patients receiving chemotherapy but not in those without chemotherapy. In addition, the combined analysis of the two SNPs conferred a 2.84-fold (95% CI = 1.50-5.37, P = 0.001) increased risk of recurrence and/or death. Similarly, this effect was only prominent in those receiving chemotherapy (P < 0.001) but not in those without chemotherapy (P = 0.999).
Our data suggest that genetic polymorphisms in pre-miRNA genes may impact CRC prognosis especially in patients receiving chemotherapy, a finding that warrants further independent validation.
This is one of the first studies showing a prognostic role of pre-miRNA gene SNPs in CRC. |
doi_str_mv | 10.1158/1055-9965.EPI-11-0624 |
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We analyzed the effects of seven single-nucleotide polymorphisms (SNP) in pre-miRNA genes on the prognosis of a Chinese population with 408 CRC patients with surgically-resected adenocarcinoma.
Two SNPs were identified to be significantly associated with recurrence-free survival and overall survival of the patients. The most significant SNP was rs6505162 in pre-miR-423. Compared with the homozygous wild-type genotype, the variant-containing genotypes of this SNP were significantly associated with both the overall survival (HR = 2.12, 95% CI = 1.34-3.34, P = 0.001) and the recurrence-free survival (HR = 1.59, 95% CI = 1.08-2.36, P = 0.019). Another SNP, rs4919510 in pre-miR-608, was also associated with altered recurrence-free survival (HR = 0.61, 95% CI = 0.41-0.92, P = 0.017). These effects were evident only in patients receiving chemotherapy but not in those without chemotherapy. In addition, the combined analysis of the two SNPs conferred a 2.84-fold (95% CI = 1.50-5.37, P = 0.001) increased risk of recurrence and/or death. Similarly, this effect was only prominent in those receiving chemotherapy (P < 0.001) but not in those without chemotherapy (P = 0.999).
Our data suggest that genetic polymorphisms in pre-miRNA genes may impact CRC prognosis especially in patients receiving chemotherapy, a finding that warrants further independent validation.
This is one of the first studies showing a prognostic role of pre-miRNA gene SNPs in CRC.</description><identifier>ISSN: 1055-9965</identifier><identifier>EISSN: 1538-7755</identifier><identifier>DOI: 10.1158/1055-9965.EPI-11-0624</identifier><identifier>PMID: 22028396</identifier><identifier>CODEN: CEBPE4</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Colorectal Neoplasms - genetics ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Genotype ; Humans ; Male ; Medical sciences ; MicroRNAs - genetics ; Middle Aged ; Polymorphism, Single Nucleotide ; Prognosis ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors ; Young Adult</subject><ispartof>Cancer epidemiology, biomarkers & prevention, 2012-01, Vol.21 (1), p.217-227</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-a897e3c8f51a7cf3b5d0560e18ccdbd8aeed3e5ed99636d1d1104cdbed402dab3</citedby><cites>FETCH-LOGICAL-c473t-a897e3c8f51a7cf3b5d0560e18ccdbd8aeed3e5ed99636d1d1104cdbed402dab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3356,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25523768$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22028396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>JINLIANG XING</creatorcontrib><creatorcontrib>SHAOGUI WAN</creatorcontrib><creatorcontrib>HUSHAN YANG</creatorcontrib><creatorcontrib>FENG ZHOU</creatorcontrib><creatorcontrib>FALIN QU</creatorcontrib><creatorcontrib>BINGSHAN LI</creatorcontrib><creatorcontrib>MYERS, Ronald E</creatorcontrib><creatorcontrib>XIAOYING FU</creatorcontrib><creatorcontrib>PALAZZO, Juan P</creatorcontrib><creatorcontrib>XIANLI HE</creatorcontrib><creatorcontrib>ZHINAN CHEN</creatorcontrib><title>Genetic Polymorphisms in Pre-microRNA Genes as Prognostic Markers of Colorectal Cancer</title><title>Cancer epidemiology, biomarkers & prevention</title><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><description>Cumulative data have shown that microRNAs (miRNA) are involved in the etiology and prognosis of colorectal cancer (CRC). Genetic polymorphisms in pre-miRNA genes may influence the biogenesis and functions of their host miRNAs. However, whether these polymorphisms are associated with CRC prognosis remains unknown.
We analyzed the effects of seven single-nucleotide polymorphisms (SNP) in pre-miRNA genes on the prognosis of a Chinese population with 408 CRC patients with surgically-resected adenocarcinoma.
Two SNPs were identified to be significantly associated with recurrence-free survival and overall survival of the patients. The most significant SNP was rs6505162 in pre-miR-423. Compared with the homozygous wild-type genotype, the variant-containing genotypes of this SNP were significantly associated with both the overall survival (HR = 2.12, 95% CI = 1.34-3.34, P = 0.001) and the recurrence-free survival (HR = 1.59, 95% CI = 1.08-2.36, P = 0.019). Another SNP, rs4919510 in pre-miR-608, was also associated with altered recurrence-free survival (HR = 0.61, 95% CI = 0.41-0.92, P = 0.017). These effects were evident only in patients receiving chemotherapy but not in those without chemotherapy. In addition, the combined analysis of the two SNPs conferred a 2.84-fold (95% CI = 1.50-5.37, P = 0.001) increased risk of recurrence and/or death. Similarly, this effect was only prominent in those receiving chemotherapy (P < 0.001) but not in those without chemotherapy (P = 0.999).
Our data suggest that genetic polymorphisms in pre-miRNA genes may impact CRC prognosis especially in patients receiving chemotherapy, a finding that warrants further independent validation.
This is one of the first studies showing a prognostic role of pre-miRNA gene SNPs in CRC.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>MicroRNAs - genetics</subject><subject>Middle Aged</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prognosis</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><subject>Young Adult</subject><issn>1055-9965</issn><issn>1538-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9P3DAQxa0KVGDLR2iVSwWXLHacSewL0mpFAWlbVlXL1fLak8VtEi92thLfHkcsf3rhZGvm90Yz7xHymdEpYyDOGAXIpaxgerG8zhnLaVWUH8ghAy7yugbYS_9n5oAcxfiHUlpLgI_koChoIbisDsntJfY4OJMtffvQ-bC5c7GLmeuzZcC8cyb4nz9m2UjFTMdU9evex1HxXYe_GGLmm2zuWx_QDLrN5ro3GD6R_Ua3EY9374T8_nbxa36VL24ur-ezRW7Kmg-5FrJGbkQDTNem4SuwFCqKTBhjV1ZoRMsR0KYjeGWZZYyWqYO2pIXVKz4h509zN9tVh9ZgPwTdqk1wnQ4Pymun_u_07k6t_T_FC-ASyjTgZDcg-PstxkF1LhpsW92j30YlGdCSJecSefouyUouCw5SyITCE5rcizFg87IQo2pMT43JqDEZldJLJTWml3Rf3l7zonqOKwFfd4CORrdNSGa7-MoBFLyuBH8EEJWk3A</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>JINLIANG XING</creator><creator>SHAOGUI WAN</creator><creator>HUSHAN YANG</creator><creator>FENG ZHOU</creator><creator>FALIN QU</creator><creator>BINGSHAN LI</creator><creator>MYERS, Ronald E</creator><creator>XIAOYING FU</creator><creator>PALAZZO, Juan P</creator><creator>XIANLI HE</creator><creator>ZHINAN CHEN</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><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>7TM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120101</creationdate><title>Genetic Polymorphisms in Pre-microRNA Genes as Prognostic Markers of Colorectal Cancer</title><author>JINLIANG XING ; SHAOGUI WAN ; HUSHAN YANG ; FENG ZHOU ; FALIN QU ; BINGSHAN LI ; MYERS, Ronald E ; XIAOYING FU ; PALAZZO, Juan P ; XIANLI HE ; ZHINAN CHEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-a897e3c8f51a7cf3b5d0560e18ccdbd8aeed3e5ed99636d1d1104cdbed402dab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>MicroRNAs - genetics</topic><topic>Middle Aged</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Prognosis</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>JINLIANG XING</creatorcontrib><creatorcontrib>SHAOGUI WAN</creatorcontrib><creatorcontrib>HUSHAN YANG</creatorcontrib><creatorcontrib>FENG ZHOU</creatorcontrib><creatorcontrib>FALIN QU</creatorcontrib><creatorcontrib>BINGSHAN LI</creatorcontrib><creatorcontrib>MYERS, Ronald E</creatorcontrib><creatorcontrib>XIAOYING FU</creatorcontrib><creatorcontrib>PALAZZO, Juan P</creatorcontrib><creatorcontrib>XIANLI HE</creatorcontrib><creatorcontrib>ZHINAN CHEN</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JINLIANG XING</au><au>SHAOGUI WAN</au><au>HUSHAN YANG</au><au>FENG ZHOU</au><au>FALIN QU</au><au>BINGSHAN LI</au><au>MYERS, Ronald E</au><au>XIAOYING FU</au><au>PALAZZO, Juan P</au><au>XIANLI HE</au><au>ZHINAN CHEN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic Polymorphisms in Pre-microRNA Genes as Prognostic Markers of Colorectal Cancer</atitle><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>21</volume><issue>1</issue><spage>217</spage><epage>227</epage><pages>217-227</pages><issn>1055-9965</issn><eissn>1538-7755</eissn><coden>CEBPE4</coden><abstract>Cumulative data have shown that microRNAs (miRNA) are involved in the etiology and prognosis of colorectal cancer (CRC). Genetic polymorphisms in pre-miRNA genes may influence the biogenesis and functions of their host miRNAs. However, whether these polymorphisms are associated with CRC prognosis remains unknown.
We analyzed the effects of seven single-nucleotide polymorphisms (SNP) in pre-miRNA genes on the prognosis of a Chinese population with 408 CRC patients with surgically-resected adenocarcinoma.
Two SNPs were identified to be significantly associated with recurrence-free survival and overall survival of the patients. The most significant SNP was rs6505162 in pre-miR-423. Compared with the homozygous wild-type genotype, the variant-containing genotypes of this SNP were significantly associated with both the overall survival (HR = 2.12, 95% CI = 1.34-3.34, P = 0.001) and the recurrence-free survival (HR = 1.59, 95% CI = 1.08-2.36, P = 0.019). Another SNP, rs4919510 in pre-miR-608, was also associated with altered recurrence-free survival (HR = 0.61, 95% CI = 0.41-0.92, P = 0.017). These effects were evident only in patients receiving chemotherapy but not in those without chemotherapy. In addition, the combined analysis of the two SNPs conferred a 2.84-fold (95% CI = 1.50-5.37, P = 0.001) increased risk of recurrence and/or death. Similarly, this effect was only prominent in those receiving chemotherapy (P < 0.001) but not in those without chemotherapy (P = 0.999).
Our data suggest that genetic polymorphisms in pre-miRNA genes may impact CRC prognosis especially in patients receiving chemotherapy, a finding that warrants further independent validation.
This is one of the first studies showing a prognostic role of pre-miRNA gene SNPs in CRC.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>22028396</pmid><doi>10.1158/1055-9965.EPI-11-0624</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Biological and medical sciences Colorectal Neoplasms - genetics Female Gastroenterology. Liver. Pancreas. Abdomen Genotype Humans Male Medical sciences MicroRNAs - genetics Middle Aged Polymorphism, Single Nucleotide Prognosis Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors Young Adult |
title | Genetic Polymorphisms in Pre-microRNA Genes as Prognostic Markers of Colorectal Cancer |
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