| Literature DB >> 26279761 |
Gregory M Hayes1, Belinda Cairns1, Zoia Levashova1, Lawrence Chinn1, Myra Perez1, Jan-Willem Theunissen2, Sindy Liao-Chan2, Abel Bermudez2, Mark R Flory2, Karl J Schweighofer2, Edward H van der Horst1.
Abstract
Soft tissue sarcoma (STS) is a heterogenous tumor arising from the embryonic mesoderm represented by approximately 50 histological subtypes. Effective therapeutic intervention is lacking for recurrent, late stage and metastatic disease. CD39, a cell-surface ectonucleotidase, has previously been shown to be upregulated in hematological malignancies and various epithelial tumors, but not in STS. Here, we show by mass spectrometry and immunohistochemistry that CD39 is highly expressed in primary patient sarcoma samples. Moreover, CD39 nucleotidase activity is enhanced in fibrosarcoma compared with normal control cells. We demonstrate that an inhibitory monoclonal anti-CD39 antibody, abrogates CD39 enzymatic activity significantly and prolongs survival in a lethal metastatic patient-derived sarcoma model. Taken together, the data suggest CD39 is a novel therapeutic target for the treatment of STS.Entities:
Keywords: CD39; Soft tissue sarcoma; immunohistochemistry; in vivo efficacy; mass spectrometry; monoclonal antibody
Year: 2015 PMID: 26279761 PMCID: PMC4532750
Source DB: PubMed Journal: Am J Transl Res Impact factor: 4.060