Article: Loss/down-regulation of tumor suppressor in lung cancer 1 expression is associated with tumor progression and is a biomarker of poor prognosis in ovarian carcinoma

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TitleLoss/down-regulation of tumor suppressor in lung cancer 1 expression is associated with tumor progression and is a biomarker of poor prognosis in ovarian carcinoma
AuthorsYang, G1
He, W1
Cai, M1
Luo, F1
Kung, H1
Guan, X1
Zeng, Y1
Xie, D1
KeywordsImmunohistochemistry
Ovarian tumor
Prognosis
TSLC1
Issue Date2011
PublisherLippincott Williams & Wilkins. The Journal's web site is located at tp://www.ijgc.net/
CitationInternational Journal Of Gynecological Cancer, 2011, v. 21 n. 3, p. 486-493 [How to Cite?]
DOI: http://dx.doi.org/10.1097/IGC.0b013e31820fa168
AbstractObjectives: The tumor suppressor in lung cancer 1 (TSLC1) has been identified as a putative tumor suppressor gene in non-small cell lung cancer. Although loss of TSLC1 has been observed in a number of human malignancies, the expression levels of TSLC1 gene in ovarian cancer and its clinical or prognostic significance have not been investigated. Methods: Protein expression levels of TSLC1 was explored by semiquantitative immunohistochemical staining on archival formalin-fixed, paraffin-embedded pathological specimen consisting of 30 normal ovaries, 30 ovarian cystadenomas, 40 borderline ovarian tumors, and 160 invasive ovarian carcinomas. The TSLC1 immunohistochemical staining results were then correlated with various clinicopathologic parameters and patient prognosis using various statistical models. Results: Significantly decreased, or complete loss of, protein expression of the TSLC1 gene was observed in 59%ovarian carcinomas, 45% borderline tumors, and 7% cystadenomas, but in none of the normal ovaries (0%). In ovarian carcinomas, decreased TSLC1 expression was significantly correlated with lymph node metastasis (pN, P = 0.001), distant metastasis (pM, P = 0.028), and more advanced International Federation of Gynecology and Obstetrics stages (P = 0.008). By univariate survival analysis on the ovarian carcinoma cohorts, decreased TSLC1 protein expression was significantly associated with shortened patient survival (mean: 26.9 months in tumors with complete loss of TSLC1 vs 63.1 months in tumors with significantly decreased TSLC1 vs 94.3 months in tumors with normal levels of TSLC1; P < 0.001). By multivariate analysis, TSLC1 protein expression remained as a significant and independent prognostic factor for the prediction of patient survival (P = 0.003). Conclusions: Decreased protein expression of the TSLC1 gene might be important in conferring a more aggressive behavior in ovarian carcinoma. Thus, TSLC1 may be used as an independent prognostic molecular marker for patients with ovarian carcinoma. Copyright © 2011 by IGCS and ESGO.
ISSN1048-891X
2011 Impact Factor: 1.646
2011 SCImago Journal Rankings: 0.181
DOIhttp://dx.doi.org/10.1097/IGC.0b013e31820fa168
ISI Accession Number IDWOS:000288743700011
Funding AgencyGrant Number
Nature Science Foundation of China30772334
973 Project of China2010CB912802
2010CB529401
Guangdong Science and Technology Agency2004B35001004
Funding Information:

This study was supported by the grants from the Nature Science Foundation of China (no. 30772334), the 973 Project of China (no. 2010CB912802 and 2010CB529401), and Project of Guangdong Science and Technology Agency (no. 2004B35001004).

ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorYang, G
dc.contributor.authorHe, W
dc.contributor.authorCai, M
dc.contributor.authorLuo, F
dc.contributor.authorKung, H
dc.contributor.authorGuan, X
dc.contributor.authorZeng, Y
dc.contributor.authorXie, D
dc.date.accessioned2011-08-26T14:22:13Z
dc.date.available2011-08-26T14:22:13Z
dc.date.issued2011
dc.description.abstractObjectives: The tumor suppressor in lung cancer 1 (TSLC1) has been identified as a putative tumor suppressor gene in non-small cell lung cancer. Although loss of TSLC1 has been observed in a number of human malignancies, the expression levels of TSLC1 gene in ovarian cancer and its clinical or prognostic significance have not been investigated. Methods: Protein expression levels of TSLC1 was explored by semiquantitative immunohistochemical staining on archival formalin-fixed, paraffin-embedded pathological specimen consisting of 30 normal ovaries, 30 ovarian cystadenomas, 40 borderline ovarian tumors, and 160 invasive ovarian carcinomas. The TSLC1 immunohistochemical staining results were then correlated with various clinicopathologic parameters and patient prognosis using various statistical models. Results: Significantly decreased, or complete loss of, protein expression of the TSLC1 gene was observed in 59%ovarian carcinomas, 45% borderline tumors, and 7% cystadenomas, but in none of the normal ovaries (0%). In ovarian carcinomas, decreased TSLC1 expression was significantly correlated with lymph node metastasis (pN, P = 0.001), distant metastasis (pM, P = 0.028), and more advanced International Federation of Gynecology and Obstetrics stages (P = 0.008). By univariate survival analysis on the ovarian carcinoma cohorts, decreased TSLC1 protein expression was significantly associated with shortened patient survival (mean: 26.9 months in tumors with complete loss of TSLC1 vs 63.1 months in tumors with significantly decreased TSLC1 vs 94.3 months in tumors with normal levels of TSLC1; P < 0.001). By multivariate analysis, TSLC1 protein expression remained as a significant and independent prognostic factor for the prediction of patient survival (P = 0.003). Conclusions: Decreased protein expression of the TSLC1 gene might be important in conferring a more aggressive behavior in ovarian carcinoma. Thus, TSLC1 may be used as an independent prognostic molecular marker for patients with ovarian carcinoma. Copyright © 2011 by IGCS and ESGO.
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationInternational Journal Of Gynecological Cancer, 2011, v. 21 n. 3, p. 486-493 [How to Cite?]
DOI: http://dx.doi.org/10.1097/IGC.0b013e31820fa168
dc.identifier.doihttp://dx.doi.org/10.1097/IGC.0b013e31820fa168
dc.identifier.epage493
dc.identifier.hkuros190875
dc.identifier.isiWOS:000288743700011
Funding AgencyGrant Number
Nature Science Foundation of China30772334
973 Project of China2010CB912802
2010CB529401
Guangdong Science and Technology Agency2004B35001004
Funding Information:

This study was supported by the grants from the Nature Science Foundation of China (no. 30772334), the 973 Project of China (no. 2010CB912802 and 2010CB529401), and Project of Guangdong Science and Technology Agency (no. 2004B35001004).

dc.identifier.issn1048-891X
2011 Impact Factor: 1.646
2011 SCImago Journal Rankings: 0.181
dc.identifier.issue3
dc.identifier.scopuseid_2-s2.0-80051647936
dc.identifier.spage486
dc.identifier.urihttp://hdl.handle.net/10722/137271
dc.identifier.volume21
dc.languageeng
dc.publisherLippincott Williams & Wilkins. The Journal's web site is located at tp://www.ijgc.net/
dc.publisher.placeUnited States
dc.relation.ispartofInternational Journal of Gynecological Cancer
dc.relation.referencesReferences in Scopus
dc.subject.meshAdenocarcinoma, Mucinous - metabolism - pathology
dc.subject.meshCell Adhesion Molecules - metabolism
dc.subject.meshCystadenocarcinoma, Serous - metabolism - pathology
dc.subject.meshImmunoglobulins - metabolism
dc.subject.meshOvarian Neoplasms - metabolism - pathology
dc.subjectImmunohistochemistry
dc.subjectOvarian tumor
dc.subjectPrognosis
dc.subjectTSLC1
dc.titleLoss/down-regulation of tumor suppressor in lung cancer 1 expression is associated with tumor progression and is a biomarker of poor prognosis in ovarian carcinoma
dc.typeArticle
Author Affiliations
  1. Sun Yat-Sen University