Cited 70 times in
MICA/B and ULBP1 NKG2D ligands are independent predictors of good prognosis in cervical cancer.
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김성훈 | - |
dc.contributor.author | 김재훈 | - |
dc.contributor.author | 조한별 | - |
dc.date.accessioned | 2015-12-28T11:07:12Z | - |
dc.date.available | 2015-12-28T11:07:12Z | - |
dc.date.issued | 2014 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/138734 | - |
dc.description.abstract | Background : NKG2D (natural killer group 2, member D) is thought to play an important role in mediating the activation of anticancer immune response. Expression of NKG2D ligands (NKG2DLs) is pronounced in malignancies and the heterogeneity of NKG2DL expression remains unclear. Here, we investigate the expression and clinical significance of NKG2DLs in cervical cancer. Methods : Immunohistochemical analyses of MICA/B, ULBP1, ULBP2, ULBP3, RAET1E, and RAET1G were performed using tissue microarray analysis of 200 cervical cancers, 327 high-grade cervical intraepithelial neoplasias (CINs), 99 low-grade CINs, and 541 matched nonadjacent normal cervical epithelial tissues and compared the data with clinicopathologic variables, including the survival of cervical cancer patients. Results : MICA/B, ULBP1, and RAET1E expression was higher in cervical cancer than in low-grade CIN (p < 0.001, p = 0.012, p = 0.013, respectively) and normal cervix (all p < 0.001). Among these markers, expression of ULBP1 was significantly different depending on patient tumor stage (p = 0.010) and tumor size (p = 0.045). ULBP1 expression was correlated with MICA/B (p < 0.001) and ULBP2 (p = 0.002) expression in cervical cancer. While MICA/B+ or ULBP1+ patients had improved disease-free survival time (p = 0.027 and p = 0.009, respectively) relative to that of the low expression group, RAET1E+ or RAET1G+ was correlated with shorter survival time (p = 0.018 and p = 0.029, respectively). However, in terms of overall survival, the ULBP1+ group had significantly longer survival time than the low expression group (p = 0.009). Multivariate analysis indicated that MICA/B+/ULBP1+ (HR = 0.16, p = 0.015) and ULBP1+ (HR = 0.31, p = 0.024) are independent prognostic factors of disease-free survival in cervical cancer. Conclusions : High expression of either ULBP1 or MICA/B and ULBP1 combined is an indicator of good prognosis in cervical cancer, suggesting their potential utility as prognostic tests in clinical assessment. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 1~11 | - |
dc.relation.isPartOf | BMC CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Biomarkers, Tumor/analysis* | - |
dc.subject.MESH | Carrier Proteins/analysis | - |
dc.subject.MESH | Cervical Intraepithelial Neoplasia/chemistry* | - |
dc.subject.MESH | Cervical Intraepithelial Neoplasia/pathology | - |
dc.subject.MESH | Cervix Uteri/chemistry | - |
dc.subject.MESH | Disease-Free Survival | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | GPI-Linked Proteins/analysis | - |
dc.subject.MESH | HeLa Cells | - |
dc.subject.MESH | Histocompatibility Antigens Class I/analysis* | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Intercellular Signaling Peptides and Proteins/analysis | - |
dc.subject.MESH | Intracellular Signaling Peptides and Proteins/analysis* | - |
dc.subject.MESH | Ligands | - |
dc.subject.MESH | Membrane Proteins/analysis | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | NK Cell Lectin-Like Receptor Subfamily K/analysis* | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Survival Rate | - |
dc.subject.MESH | Tissue Array Analysis | - |
dc.subject.MESH | Tumor Burden | - |
dc.subject.MESH | Uterine Cervical Neoplasms/chemistry* | - |
dc.subject.MESH | Uterine Cervical Neoplasms/pathology | - |
dc.title | MICA/B and ULBP1 NKG2D ligands are independent predictors of good prognosis in cervical cancer. | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Obstetrics & Gynecology (산부인과학) | - |
dc.contributor.googleauthor | Hanbyoul Cho | - |
dc.contributor.googleauthor | Joon Yong Chung | - |
dc.contributor.googleauthor | Sunghoon Kim | - |
dc.contributor.googleauthor | Till Braunschweig | - |
dc.contributor.googleauthor | Tae Heung Kang | - |
dc.contributor.googleauthor | Jennie Kim | - |
dc.contributor.googleauthor | Eun Joo Chung | - |
dc.contributor.googleauthor | Stephen M Hewitt | - |
dc.contributor.googleauthor | Jae Hoon Kim | - |
dc.identifier.doi | 10.1186/1471-2407-14-957 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00595 | - |
dc.contributor.localId | A00876 | - |
dc.contributor.localId | A03921 | - |
dc.relation.journalcode | J00351 | - |
dc.identifier.eissn | 1471-2407 | - |
dc.identifier.pmid | 25510288 | - |
dc.subject.keyword | Cervical cancer | - |
dc.subject.keyword | Tissue microarray | - |
dc.subject.keyword | Immunohistochemistry | - |
dc.subject.keyword | NKG2D ligands | - |
dc.contributor.alternativeName | Kim, Sung Hoon | - |
dc.contributor.alternativeName | Kim, Jae Hoon | - |
dc.contributor.alternativeName | Cho, Han Byoul | - |
dc.contributor.affiliatedAuthor | Kim, Sung Hoon | - |
dc.contributor.affiliatedAuthor | Kim, Jae Hoon | - |
dc.contributor.affiliatedAuthor | Cho, Han Byoul | - |
dc.citation.volume | 14 | - |
dc.citation.number | 957 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 11 | - |
dc.identifier.bibliographicCitation | BMC CANCER, Vol.14(957) : 1-11, 2014 | - |
dc.identifier.rimsid | 38848 | - |
dc.type.rims | ART | - |
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