Soluble MICA and a MICA variation as possible prognostic biomarkers for HBV-induced hepatocellular carcinoma

MHC class I polypeptide-related chain A (MICA) molecule is induced in response to viral infection and various types of stress. We recently reported that a single nucleotide polymorphism (SNP) rs2596542 located in the MICA promoter region was significantly associated with the risk for hepatitis C vir...

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Veröffentlicht in:PloS one 2012-09, Vol.7 (9), p.e44743
Hauptverfasser: Kumar, Vinod, Yi Lo, Paulisally Hau, Sawai, Hiromi, Kato, Naoya, Takahashi, Atsushi, Deng, Zhenzhong, Urabe, Yuji, Mbarek, Hamdi, Tokunaga, Katsushi, Tanaka, Yasuhito, Sugiyama, Masaya, Mizokami, Masashi, Muroyama, Ryosuke, Tateishi, Ryosuke, Omata, Masao, Koike, Kazuhiko, Tanikawa, Chizu, Kamatani, Naoyuki, Kubo, Michiaki, Nakamura, Yusuke, Matsuda, Koichi
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container_issue 9
container_start_page e44743
container_title PloS one
container_volume 7
creator Kumar, Vinod
Yi Lo, Paulisally Hau
Sawai, Hiromi
Kato, Naoya
Takahashi, Atsushi
Deng, Zhenzhong
Urabe, Yuji
Mbarek, Hamdi
Tokunaga, Katsushi
Tanaka, Yasuhito
Sugiyama, Masaya
Mizokami, Masashi
Muroyama, Ryosuke
Tateishi, Ryosuke
Omata, Masao
Koike, Kazuhiko
Tanikawa, Chizu
Kamatani, Naoyuki
Kubo, Michiaki
Nakamura, Yusuke
Matsuda, Koichi
description MHC class I polypeptide-related chain A (MICA) molecule is induced in response to viral infection and various types of stress. We recently reported that a single nucleotide polymorphism (SNP) rs2596542 located in the MICA promoter region was significantly associated with the risk for hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) and also with serum levels of soluble MICA (sMICA). In this study, we focused on the possible involvement of MICA in liver carcinogenesis related to hepatitis B virus (HBV) infection and examined correlation between the MICA polymorphism and the serum sMICA levels in HBV-induced HCC patients. The genetic association analysis revealed a nominal association with an SNP rs2596542; a G allele was considered to increase the risk of HBV-induced HCC (P = 0.029 with odds ratio of 1.19). We also found a significant elevation of sMICA in HBV-induced HCC cases. Moreover, a G allele of SNP rs2596542 was significantly associated with increased sMICA levels (P = 0.009). Interestingly, HCC patients with the high serum level of sMICA (>5 pg/ml) exhibited poorer prognosis than those with the low serum level of sMICA (≤5 pg/ml) (P = 0.008). Thus, our results highlight the importance of MICA genetic variations and the significance of sMICA as a predictive biomarker for HBV-induced HCC.
doi_str_mv 10.1371/journal.pone.0044743
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We recently reported that a single nucleotide polymorphism (SNP) rs2596542 located in the MICA promoter region was significantly associated with the risk for hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) and also with serum levels of soluble MICA (sMICA). In this study, we focused on the possible involvement of MICA in liver carcinogenesis related to hepatitis B virus (HBV) infection and examined correlation between the MICA polymorphism and the serum sMICA levels in HBV-induced HCC patients. The genetic association analysis revealed a nominal association with an SNP rs2596542; a G allele was considered to increase the risk of HBV-induced HCC (P = 0.029 with odds ratio of 1.19). We also found a significant elevation of sMICA in HBV-induced HCC cases. Moreover, a G allele of SNP rs2596542 was significantly associated with increased sMICA levels (P = 0.009). Interestingly, HCC patients with the high serum level of sMICA (&gt;5 pg/ml) exhibited poorer prognosis than those with the low serum level of sMICA (≤5 pg/ml) (P = 0.008). Thus, our results highlight the importance of MICA genetic variations and the significance of sMICA as a predictive biomarker for HBV-induced HCC.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0044743</identifier><identifier>PMID: 23024757</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Aged ; Alleles ; Analysis ; Association analysis ; Bioindicators ; Biology ; Biomarkers ; Biomarkers, Tumor - blood ; Biomarkers, Tumor - genetics ; Carcinogenesis ; Carcinogens ; Carcinoma, Hepatocellular - blood ; Carcinoma, Hepatocellular - genetics ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - virology ; Deoxyribonucleic acid ; Disease control ; DNA ; Female ; Gastroenterology ; Gene polymorphism ; Genetic analysis ; Genetic aspects ; Genetic diversity ; Genetic testing ; Genomes ; Health aspects ; Hepatitis ; Hepatitis B ; Hepatitis B virus ; Hepatitis C ; Hepatitis C virus ; Hepatocellular carcinoma ; Histocompatibility Antigens Class I - blood ; Histocompatibility Antigens Class I - genetics ; Humans ; Immunology ; Infection ; Infections ; Laboratories ; Ligands ; Liver ; Liver cancer ; Liver Neoplasms - blood ; Liver Neoplasms - genetics ; Liver Neoplasms - mortality ; Liver Neoplasms - virology ; Lymphocytes ; Major histocompatibility complex ; Male ; Medical prognosis ; Medicine ; MICA protein ; Middle Aged ; Minisatellite Repeats ; Neovascularization, Pathologic - blood ; Neovascularization, Pathologic - genetics ; Pathogenesis ; Patients ; Polymorphism ; Polymorphism, Single Nucleotide ; Prognosis ; Science ; Serum levels ; Single nucleotide polymorphisms ; Single-nucleotide polymorphism ; Viral infections ; Viruses</subject><ispartof>PloS one, 2012-09, Vol.7 (9), p.e44743</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Kumar et al. 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We recently reported that a single nucleotide polymorphism (SNP) rs2596542 located in the MICA promoter region was significantly associated with the risk for hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) and also with serum levels of soluble MICA (sMICA). In this study, we focused on the possible involvement of MICA in liver carcinogenesis related to hepatitis B virus (HBV) infection and examined correlation between the MICA polymorphism and the serum sMICA levels in HBV-induced HCC patients. The genetic association analysis revealed a nominal association with an SNP rs2596542; a G allele was considered to increase the risk of HBV-induced HCC (P = 0.029 with odds ratio of 1.19). We also found a significant elevation of sMICA in HBV-induced HCC cases. Moreover, a G allele of SNP rs2596542 was significantly associated with increased sMICA levels (P = 0.009). Interestingly, HCC patients with the high serum level of sMICA (&gt;5 pg/ml) exhibited poorer prognosis than those with the low serum level of sMICA (≤5 pg/ml) (P = 0.008). Thus, our results highlight the importance of MICA genetic variations and the significance of sMICA as a predictive biomarker for HBV-induced HCC.</description><subject>Adult</subject><subject>Aged</subject><subject>Alleles</subject><subject>Analysis</subject><subject>Association analysis</subject><subject>Bioindicators</subject><subject>Biology</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - blood</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Carcinogenesis</subject><subject>Carcinogens</subject><subject>Carcinoma, Hepatocellular - blood</subject><subject>Carcinoma, Hepatocellular - genetics</subject><subject>Carcinoma, Hepatocellular - mortality</subject><subject>Carcinoma, Hepatocellular - virology</subject><subject>Deoxyribonucleic acid</subject><subject>Disease control</subject><subject>DNA</subject><subject>Female</subject><subject>Gastroenterology</subject><subject>Gene polymorphism</subject><subject>Genetic analysis</subject><subject>Genetic aspects</subject><subject>Genetic diversity</subject><subject>Genetic testing</subject><subject>Genomes</subject><subject>Health aspects</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Hepatitis B virus</subject><subject>Hepatitis C</subject><subject>Hepatitis C virus</subject><subject>Hepatocellular carcinoma</subject><subject>Histocompatibility Antigens Class I - blood</subject><subject>Histocompatibility Antigens Class I - genetics</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infection</subject><subject>Infections</subject><subject>Laboratories</subject><subject>Ligands</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - mortality</subject><subject>Liver Neoplasms - virology</subject><subject>Lymphocytes</subject><subject>Major histocompatibility 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Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Vinod</au><au>Yi Lo, Paulisally Hau</au><au>Sawai, Hiromi</au><au>Kato, Naoya</au><au>Takahashi, Atsushi</au><au>Deng, Zhenzhong</au><au>Urabe, Yuji</au><au>Mbarek, Hamdi</au><au>Tokunaga, Katsushi</au><au>Tanaka, Yasuhito</au><au>Sugiyama, Masaya</au><au>Mizokami, Masashi</au><au>Muroyama, Ryosuke</au><au>Tateishi, Ryosuke</au><au>Omata, Masao</au><au>Koike, Kazuhiko</au><au>Tanikawa, Chizu</au><au>Kamatani, Naoyuki</au><au>Kubo, Michiaki</au><au>Nakamura, Yusuke</au><au>Matsuda, Koichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soluble MICA and a MICA variation as possible prognostic biomarkers for HBV-induced hepatocellular carcinoma</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-09-14</date><risdate>2012</risdate><volume>7</volume><issue>9</issue><spage>e44743</spage><pages>e44743-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>MHC class I polypeptide-related chain A (MICA) molecule is induced in response to viral infection and various types of stress. We recently reported that a single nucleotide polymorphism (SNP) rs2596542 located in the MICA promoter region was significantly associated with the risk for hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) and also with serum levels of soluble MICA (sMICA). In this study, we focused on the possible involvement of MICA in liver carcinogenesis related to hepatitis B virus (HBV) infection and examined correlation between the MICA polymorphism and the serum sMICA levels in HBV-induced HCC patients. The genetic association analysis revealed a nominal association with an SNP rs2596542; a G allele was considered to increase the risk of HBV-induced HCC (P = 0.029 with odds ratio of 1.19). We also found a significant elevation of sMICA in HBV-induced HCC cases. Moreover, a G allele of SNP rs2596542 was significantly associated with increased sMICA levels (P = 0.009). Interestingly, HCC patients with the high serum level of sMICA (&gt;5 pg/ml) exhibited poorer prognosis than those with the low serum level of sMICA (≤5 pg/ml) (P = 0.008). Thus, our results highlight the importance of MICA genetic variations and the significance of sMICA as a predictive biomarker for HBV-induced HCC.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23024757</pmid><doi>10.1371/journal.pone.0044743</doi><tpages>e44743</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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issn 1932-6203
1932-6203
language eng
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source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS)
subjects Adult
Aged
Alleles
Analysis
Association analysis
Bioindicators
Biology
Biomarkers
Biomarkers, Tumor - blood
Biomarkers, Tumor - genetics
Carcinogenesis
Carcinogens
Carcinoma, Hepatocellular - blood
Carcinoma, Hepatocellular - genetics
Carcinoma, Hepatocellular - mortality
Carcinoma, Hepatocellular - virology
Deoxyribonucleic acid
Disease control
DNA
Female
Gastroenterology
Gene polymorphism
Genetic analysis
Genetic aspects
Genetic diversity
Genetic testing
Genomes
Health aspects
Hepatitis
Hepatitis B
Hepatitis B virus
Hepatitis C
Hepatitis C virus
Hepatocellular carcinoma
Histocompatibility Antigens Class I - blood
Histocompatibility Antigens Class I - genetics
Humans
Immunology
Infection
Infections
Laboratories
Ligands
Liver
Liver cancer
Liver Neoplasms - blood
Liver Neoplasms - genetics
Liver Neoplasms - mortality
Liver Neoplasms - virology
Lymphocytes
Major histocompatibility complex
Male
Medical prognosis
Medicine
MICA protein
Middle Aged
Minisatellite Repeats
Neovascularization, Pathologic - blood
Neovascularization, Pathologic - genetics
Pathogenesis
Patients
Polymorphism
Polymorphism, Single Nucleotide
Prognosis
Science
Serum levels
Single nucleotide polymorphisms
Single-nucleotide polymorphism
Viral infections
Viruses
title Soluble MICA and a MICA variation as possible prognostic biomarkers for HBV-induced hepatocellular carcinoma
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