Cargando…
Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells
BACKGROUND: Soft tissue sarcomas are a group of neoplasms with differentiation towards mesenchymal tissue, many of which are aggressive and chemotherapy resistant. Histology and immunoprofiles often overlap with neoplasms of other lineages, and establishing an accurate histopathological diagnosis is...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985356/ https://www.ncbi.nlm.nih.gov/pubmed/27434038 http://dx.doi.org/10.1038/bjc.2016.214 |
_version_ | 1782448051467583488 |
---|---|
author | Thway, Khin Robertson, David Jones, Robin L Selfe, Joanna Shipley, Janet Fisher, Cyril Isacke, Clare M |
author_facet | Thway, Khin Robertson, David Jones, Robin L Selfe, Joanna Shipley, Janet Fisher, Cyril Isacke, Clare M |
author_sort | Thway, Khin |
collection | PubMed |
description | BACKGROUND: Soft tissue sarcomas are a group of neoplasms with differentiation towards mesenchymal tissue, many of which are aggressive and chemotherapy resistant. Histology and immunoprofiles often overlap with neoplasms of other lineages, and establishing an accurate histopathological diagnosis is crucial for correct management, and therapeutic stratification. The endosialin cell surface glycoprotein is predominantly expressed by stromal fibroblasts and pericytes in epithelial neoplasms; however, tumour cell expression has been reported in small series of sarcomas. METHODS: We assessed endosialin expression by immunohistochemistry in a large set of 514 human soft tissue sarcomas. RESULTS: Tumour cell endosialin expression was seen in 89% of undifferentiated pleomorphic sarcomas (104/117), 77% adult fibrosarcomas/spindle cell sarcomas (20/26), 62% synovial sarcomas (37/60), 51% leiomyosarcomas (94/185) and 31% rhabdomyosarcomas (39/126). CONCLUSIONS: Endosialin immunohistochemistry has potential to distinguish undifferentiated and poorly differentiated sarcomas from other poorly differentiated, non-mesenchymal neoplasms. A Phase II trial randomising patients with advanced sarcomas to receive chemotherapy with/without an endosialin therapeutic antibody has recently completed enrolment. Endosialin expression could be used to select patients for such clinical trials. Based on our results, patients with undifferentiated pleomorphic sarcoma may be particularly suitable for such a therapeutic approach. |
format | Online Article Text |
id | pubmed-4985356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49853562016-08-29 Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells Thway, Khin Robertson, David Jones, Robin L Selfe, Joanna Shipley, Janet Fisher, Cyril Isacke, Clare M Br J Cancer Molecular Diagnostics BACKGROUND: Soft tissue sarcomas are a group of neoplasms with differentiation towards mesenchymal tissue, many of which are aggressive and chemotherapy resistant. Histology and immunoprofiles often overlap with neoplasms of other lineages, and establishing an accurate histopathological diagnosis is crucial for correct management, and therapeutic stratification. The endosialin cell surface glycoprotein is predominantly expressed by stromal fibroblasts and pericytes in epithelial neoplasms; however, tumour cell expression has been reported in small series of sarcomas. METHODS: We assessed endosialin expression by immunohistochemistry in a large set of 514 human soft tissue sarcomas. RESULTS: Tumour cell endosialin expression was seen in 89% of undifferentiated pleomorphic sarcomas (104/117), 77% adult fibrosarcomas/spindle cell sarcomas (20/26), 62% synovial sarcomas (37/60), 51% leiomyosarcomas (94/185) and 31% rhabdomyosarcomas (39/126). CONCLUSIONS: Endosialin immunohistochemistry has potential to distinguish undifferentiated and poorly differentiated sarcomas from other poorly differentiated, non-mesenchymal neoplasms. A Phase II trial randomising patients with advanced sarcomas to receive chemotherapy with/without an endosialin therapeutic antibody has recently completed enrolment. Endosialin expression could be used to select patients for such clinical trials. Based on our results, patients with undifferentiated pleomorphic sarcoma may be particularly suitable for such a therapeutic approach. Nature Publishing Group 2016-08-09 2016-07-19 /pmc/articles/PMC4985356/ /pubmed/27434038 http://dx.doi.org/10.1038/bjc.2016.214 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Molecular Diagnostics Thway, Khin Robertson, David Jones, Robin L Selfe, Joanna Shipley, Janet Fisher, Cyril Isacke, Clare M Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
title | Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
title_full | Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
title_fullStr | Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
title_full_unstemmed | Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
title_short | Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
title_sort | endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985356/ https://www.ncbi.nlm.nih.gov/pubmed/27434038 http://dx.doi.org/10.1038/bjc.2016.214 |
work_keys_str_mv | AT thwaykhin endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells AT robertsondavid endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells AT jonesrobinl endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells AT selfejoanna endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells AT shipleyjanet endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells AT fishercyril endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells AT isackeclarem endosialinexpressioninsofttissuesarcomaasapotentialmarkerofundifferentiatedmesenchymalcells |