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ADAM10 Is a Potential Novel Prognostic Biomarker for Sacral Chordoma.

Authors :
Ding Y
Bui MM
Wang Q
Sun X
Zhang M
Niu X
Tian W
Source :
Annals of clinical and laboratory science [Ann Clin Lab Sci] 2019 May; Vol. 49 (3), pp. 309-316.
Publication Year :
2019

Abstract

The ADAM (A Disintegrin and Metalloprotease) is a zinc-dependent family of transmembrane proteins upregulated in cancers. As the most frequent member, ADAM10's potential prognostic role in chordoma is unknown.<br />Objective: We investigated the expression of ADAM10 protein and its prognostic value in sacral chordoma.<br />Design: Clinical information of patients with sacral chordoma diagnosis during a 7-year period and their archived pathology were retrieved. Immunohistochemistry study of the expression of ADAM10 protein in sacral chordoma and control samples was conducted. The ADAM10 expression was correlated with the patients' clinicopathological information and analyzed by statistical methods.<br />Results: The average age of 64 patients was 57.6 years (range, 35-83 years). Follow-up ranged from 12 to 141 months (mean, 72 months). The histological type included 47 classic, 6 chondroid, and 11 dedifferentiated chordomas. The expression level of ADAM10 was significantly correlated with the histological type ( χ <superscript>2</superscript> =11.345, P =0.003), metastasis ( χ <superscript>2</superscript> =10.149, P =0.001), overall survival (log-rank test: χ <superscript>2</superscript> =8.177, P =0.004) and disease free survival (log-rank test: χ <superscript>2</superscript> =6.805, P =0.009). The average survival time of patients with weak expression of ADAM10 was longer than that of strong expression.<br />Conclusion: The expression of ADAM10 protein is related to the histologic type and the prognosis of sacral chordoma.<br /> (© 2019 by the Association of Clinical Scientists, Inc.)

Details

Language :
English
ISSN :
1550-8080
Volume :
49
Issue :
3
Database :
MEDLINE
Journal :
Annals of clinical and laboratory science
Publication Type :
Academic Journal
Accession number :
31308029