Publication: Correlation between the high expression levels of cancer-germline genes with clinical characteristics in esophageal squamous cell carcinoma
Authors
Chen, Xinfeng ; Wang, Liping ; Yue, Dongli ; Liu, Jinyan ; Huang, Lan ; Yang, Li ; Cao, Ling ; Qin, Guohui ; Li, Anqi ; Wang, Dan ; Wang, Meng ; Qi, Yu ; Zhang, Bin ; van der Bruggen, Pierre ; Zhang, Yi
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Publisher
Universidad de Murcia. Departamento de BiologĂa Celular e HistologĂa
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DOI
DOI: 10.14670/HH-11-847
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info:eu-repo/semantics/article
Description
Abstract
Antigens encoded by cancer-germline genes
are attractive targets for cancer immunotherapy. In this
study, we aimed to evaluate the mRNA expression of
cancer-germline genes, expression of the encoded
proteins in patients with esophageal squamous cell
carcinoma (ESCC) and their correlations with clinical
characteristics. In addition, the effects of downregulation
cancer-germline genes on ESCC cells were assessed in
vitro. Our results showed that cancer-germline genes
were frequently expressed in ESCC samples. The
positive rates of in ESCC samples were: 87% of MAGEA3, 60% of MAGE-A4, 65% of MAGE-C2, and 20% of
NY-ESO-1 at mRNA level. MAGE-A3 expression was
associated with age, lymph node metastasis and tumor
stage (all P<0.05), while MAGE-C2 expression was only
associated with tumor stage (P<0.05). Furthermore, the
MAGE-A3 expressing patients had a poorer overall
survival (P<0.05). Multivariate analysis identified
MAGE-A3 as an independent poor prognostic marker in
ESCC. In vitro assay, ESCC cell lines treated with
specific siRNAs to down-regulate MAGE-A3 and
MAGE-C2 resulted in decreased colony-formation and
migration ability (P<0.05). Epithelial marker E-cadherin
was up-regulated in siRNA-MAGE-A3/C2 cells
compared to controls, whereas mesenchymal markers
Vimentin, N-cadherin and Slug were downregulated (all
P<0.05), suggesting a role for MAGE-A3/C2 in ESCC
metastasis through inducing epithelial-mesenchymal
transition. The present study revealed that cancergermline genes and their encoded proteins were
frequently expressed in ESCC tumor samples and were
related to poor prognosis. Thus, cancer-germline genes
may serve as useful biomarkers and potential targets for
ESCC patients
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Citation
Histology and Histopathology, Vol.32, nÂş8, (2017)
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