CXCR4 Expression as a Prognostic Biomarker in Soft Tissue Sarcomas

Author:

Virgili Anna C.123ORCID,Salazar Juliana3ORCID,Gallardo Alberto4ORCID,López-Pousa Antonio13,Terés Raúl13,Bagué Silvia4ORCID,Orellana Ruth4ORCID,Fumagalli Caterina4,Mangues Ramon567ORCID,Alba-Castellón Lorena567ORCID,Unzueta Ugutz567ORCID,Casanova Isolda567,Sebio Ana13

Affiliation:

1. Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain

2. Department of Medicine, Faculty of Medicine, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain

3. Translational Medical Oncology Laboratory, Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain

4. Department of Pathology, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain

5. Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain

6. CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Bellaterra, Cerdanyola del Vallès, 08193 Barcelona, Spain

7. Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain

Abstract

Poor long-term survival in localized high-risk soft tissue sarcomas (STSs) of the extremities and trunk highlights the need to identify new prognostic factors. CXCR4 is a chemokine receptor involved in tumor progression, angiogenesis, and metastasis. The aim of this study was to evaluate the association between CXCR4 expression in tumor tissue and survival in STSs patients treated with neoadjuvant therapy. CXCR4 expression was retrospectively determined by immunohistochemical analysis in serial specimens including initial biopsies, tumors post-neoadjuvant treatment, and tumors after relapse. We found that a positive cytoplasmatic expression of CXCR4 in tumors after neoadjuvant treatment was a predictor of poor recurrence-free survival (RFS) (p = 0.003) and overall survival (p = 0.019) in synovial sarcomas. We also found that positive nuclear CXCR4 expression in the initial biopsies was associated with poor RFS (p = 0.022) in undifferentiated pleomorphic sarcomas. In conclusion, our study adds to the evidence that CXCR4 expression in tumor tissue is a promising prognostic factor for STSs.

Publisher

MDPI AG

Reference61 articles.

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