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Associations of MICB with cervical cancer in north-eastern Thais: Identification of major histocompatibility complex class I chain-related gene B motifs influencing natural killer cell activation

dc.contributor.authorA. Jumnainsongen_US
dc.contributor.authorP. Jearanaikoonen_US
dc.contributor.authorS. Khahmahpahteen_US
dc.contributor.authorW. Wongsenaen_US
dc.contributor.authorA. V. Romphruken_US
dc.contributor.authorB. Chumworathayien_US
dc.contributor.authorK. Vaeteewoottacharnen_US
dc.contributor.authorM. Ponglikitmongkolen_US
dc.contributor.authorA. Romphruken_US
dc.contributor.authorC. Leelayuwaten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.date.accessioned2018-07-12T02:29:42Z
dc.date.available2018-07-12T02:29:42Z
dc.date.issued2008-08-01en_US
dc.description.abstractThe expression of MICB, a member of the major histocompatibility complex class I chain-related gene B family, is induced in response to cellular stress. It is one of the ligands to the NKG2D receptor. MICB is polymorphic, but the distribution of MICB polymorphism in north-eastern Thais and their potential associations with cancer have not yet been elucidated. In this study, polymerase chain reaction-sequence-specific primers were developed to identify 15 MICB alleles and one group of alleles. We performed MICB typing in 100 healthy north-eastern Thai females (NETF) and 99 cervical cancer patients to evaluate the association of MICB polymorphisms and the risk of developing cervical cancer. Eight and nine alleles were detected in the NETF and cervical cancer respectively. MICB*00502 was associated negatively with a corrected P-value of 0·0009, suggesting the existence of a protective allele in cervical cancer. Amino acid substitutions carried by this allele were investigated for their potential involvement in natural killer (NK) cell activation. Although lysine at amino acid position 80 (Lys80) and aspartic acid at position 136 (Asp136) were associated negatively with cervical cancer, only MICB carrying Asp136 could induce NK cell killing more efficiently than MICB-Lys80 when the NK cells were blocked by anti-NKG2D. This result suggested that aspartic acid at position 136 may affect NKG2D binding, leading to different degrees of immune cell activation. © 2008 The Author(s).en_US
dc.identifier.citationClinical and Experimental Immunology. Vol.153, No.2 (2008), 205-213en_US
dc.identifier.doi10.1111/j.1365-2249.2008.03682.xen_US
dc.identifier.issn13652249en_US
dc.identifier.issn00099104en_US
dc.identifier.other2-s2.0-47249155307en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/19308
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=47249155307&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleAssociations of MICB with cervical cancer in north-eastern Thais: Identification of major histocompatibility complex class I chain-related gene B motifs influencing natural killer cell activationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=47249155307&origin=inwarden_US

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