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Aminopeptidase N (CD13): Expression, Prognostic Impact, and Use as Therapeutic Target for Tissue Factor Induced Tumor Vascular Infarction in Soft Tissue Sarcoma.

Authors :
Kessler T
Baumeier A
Brand C
Grau M
Angenendt L
Harrach S
Stalmann U
Schmidt LH
Gosheger G
Hardes J
Andreou D
Dreischalück J
Lenz G
Wardelmann E
Mesters RM
Schwöppe C
Berdel WE
Hartmann W
Schliemann C
Source :
Translational oncology [Transl Oncol] 2018 Dec; Vol. 11 (6), pp. 1271-1282. Date of Electronic Publication: 2018 Aug 17.
Publication Year :
2018

Abstract

Aminopeptidase N (CD13) is expressed on tumor vasculature and tumor cells. It represents a candidate for targeted therapy, e.g., by truncated tissue factor (tTF)-NGR, binding to CD13, and causing tumor vascular thrombosis. We analyzed CD13 expression by immunohistochemistry in 97 patients with STS who were treated by wide resection and uniform chemo-radio-chemotherapy. Using a semiquantitative score with four intensity levels, CD13 was expressed by tumor vasculature, or tumor cells, or both (composite value, intensity scores 1-3) in 93.9% of the STS. In 49.5% tumor cells, in 48.5% vascular/perivascular cells, and in 58.8%, composite value showed strong intensity score 3 staining. Leiomyosarcoma and synovial sarcoma showed low expression; fibrosarcoma and undifferentiated pleomorphic sarcoma showed high expression. We found a significant prognostic impact of CD13, as high expression in tumor cells or vascular/perivascular cells correlated with better relapse-free survival and overall survival. CD13 retained prognostic significance in multivariable analyses. Systemic tTF-NGR resulted in significant growth reduction of CD13-positive human HT1080 sarcoma cell line xenografts. Our results recommend further investigation of tTF-NGR in STS patients. CD13 might be a suitable predictive biomarker for patient selection.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1936-5233
Volume :
11
Issue :
6
Database :
MEDLINE
Journal :
Translational oncology
Publication Type :
Academic Journal
Accession number :
30125801
Full Text :
https://doi.org/10.1016/j.tranon.2018.08.004