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Erschienen in: Tumor Biology 12/2015

01.12.2015 | Research Article

High expression of CD39/ENTPD1 in malignant epithelial cells of human rectal adenocarcinoma

verfasst von: Bin Zhang, Bo Cheng, Feng-Sheng Li, Jian-Hua Ding, Ying-Ying Feng, Guang-Zuan Zhuo, Hua-Feng Wei, Ke Zhao

Erschienen in: Tumor Biology | Ausgabe 12/2015

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Abstract

The ectonucleotidase CD39 is pivotal in the conversion of immunostimulatory adenosine triphosphate (ATP) into immunosuppressive adenosine which potently inhibits host immune responses against cancer. This study investigated the expression level and prognostic significance of CD39 in human rectal adenocarcinoma. Our data demonstrated that CD39 staining strongly marked malignant epithelial cells where the protein and messenger RNA (mRNA) expression levels of CD39 were significantly increased compared with paracancerous controls. In addition to primary tumors, CD39 was also abundantly expressed in liver metastases and tumor-draining lymph nodes from metastatic rectal adenocarcinoma. Although patients with higher CD39 density in tumor cells were more likely to have favorable characteristics (early TNM and N stages) and overall survival, the singular parameter cannot be used as an independent factor for predicting patients’ prognosis. Intriguingly, combined analysis of CD39 and CD73 expression was more efficient to foretell patient’s outcome where patients with increased CD73 but decreased CD39 levels displayed a worst prognosis. Taken together, the current study revealed that malignant epithelial cells of human rectal adenocarcinoma strongly express CD39 that may play a potential role in the tumor invasion and metastasis. Although high expression of CD39 in tumor cells is correlated with favorable clinical outcome, the combination of CD39 and CD73 expression may have a better prognostic value.
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Metadaten
Titel
High expression of CD39/ENTPD1 in malignant epithelial cells of human rectal adenocarcinoma
verfasst von
Bin Zhang
Bo Cheng
Feng-Sheng Li
Jian-Hua Ding
Ying-Ying Feng
Guang-Zuan Zhuo
Hua-Feng Wei
Ke Zhao
Publikationsdatum
01.12.2015
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 12/2015
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-015-3683-9

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