Evidence map›Paper›PMID 21211023›Full record

ArticleJournal of experimental & clinical cancer research : CR2011

Expression and prognostic significance of cancer-testis antigens (CTA) in intrahepatic cholagiocarcinoma.

Jin-Xue Zhou, Yin Li, Sun-Xiao Chen, An-Mei Deng

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Article in Journal of experimental & clinical cancer research : CR, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

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15citing papers in PubMed, 2 pooled it
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  11. Molecular diagnosis of intrahepatic cholangiocarcinoma.Journal of hepato-biliary-pancreatic sciences · 2015
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jin-Xue ZhouDepartment of Hepatobiliary and Pancreatic Surgery, Henan Tumor Hospital, Zhengzhou, Henan 450008, PR China.
Yin Li
Sun-Xiao Chen
An-Mei Deng

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer-testis antigens (CTAs) are suitable targets for cancer-specific immunotherapy. The aim of the study is to investigate the expression of CTAs in intrahepatic cholagiocarcinoma (IHCC) and evaluate their potential therapeutic values.

methodsEighty-nine IHCC patients were retrospectively assessed for their expression of CTAs and HLA Class I by immunohistochemistry using the following antibodies: MA454 recognizing MAGE-A1, 57B recognizing multiple MAGE-A (MAGE-A3/A4), E978 recognizing NY-ESO-1, and EMR8-5 recognizing HLA class I. The clinicopathological and prognostic significance of individual CTA markers and their combination were further evaluated.

resultsThe expression rates of MAGE-A1, MAGE-A3/4 and NY-ESO-1 were 29.2%, 27.0% and 22.5%, respectively. The concomitant expression of CTAs and HLA class I antigen was observed in 33.7% of the IHCC tumors. We found that positive MAGE-3/4 expression correlated with larger tumor size (≥ 5 cm), tumor recurrence and poor prognosis. Moreover, we identified 52 cases (58.4%) of IHCC patients with at least one CTA marker expression, and this subgroup displayed a higher frequency of larger tumor size and a shorter survival than the other cases. Furthermore, expression of at least one CTA marker was also an independent prognostic factor in patients with IHCC.

conclusionOur data suggest that specific immunotherapy targeted CTAs might be a novel treatment option for IHCC patients.

Indexed as

Antigens, NeoplasmBile Duct NeoplasmsBile Ducts, IntrahepaticBiomarkers, TumorCholangiocarcinomaFemaleHLA AntigensHumansKaplan-Meier EstimateLiver NeoplasmsMaleMelanoma-Specific AntigensMembrane ProteinsMiddle AgedMultivariate AnalysisNeoplasm ProteinsAntigens, NeoplasmBiomarkers, TumorCTAG1B protein, humanHLA AntigensMAGEA1 protein, humanMAGEA3 protein, humanMAGEA4 protein, humanMelanoma-Specific AntigensMembrane ProteinsNeoplasm Proteins

Identifiers

PMID21211023
PMCPMC3023685

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.