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Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation
Oral squamous cell carcinoma (OSCC) is the most common malignant tumor of the oral cavity and is usually preceded by a range of premalignant tissue abnormalities termed oral potentially malignant disorders. Identifying malignant transformation is critical for early treatment and consequently improve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737762/ https://www.ncbi.nlm.nih.gov/pubmed/33001588 http://dx.doi.org/10.1002/cjp2.182 |
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author | Ali, Aiman Soares, Andresa Borges Eymael, Denise Magalhaes, Marco |
author_facet | Ali, Aiman Soares, Andresa Borges Eymael, Denise Magalhaes, Marco |
author_sort | Ali, Aiman |
collection | PubMed |
description | Oral squamous cell carcinoma (OSCC) is the most common malignant tumor of the oral cavity and is usually preceded by a range of premalignant tissue abnormalities termed oral potentially malignant disorders. Identifying malignant transformation is critical for early treatment and consequently improved survival and decreased morbidity. Invadopodia (INV) are specialized subcellular structures required for cancer cell invasion. We developed a new method to visualize INV in keratinocytes using fluorescent immunohistochemistry (FIHC) and semi‐automated images analysis. The presence of INV was used to determine the risk of malignant transformation. We analyzed 145 formalin‐fixed, paraffin‐embedded (FFPE) oral biopsy samples from 95 patients diagnosed as nondysplastic, dysplastic, and OSCC including 49 patients whose lesions transformed to OSCC (progressing) and 46 cases that did not transform to OSCC (control). All samples were stained for Cortactin, tyrosine kinase substrate with five SH3 domains (Tks5) and matrix metallopeptidase 14 (MMP14) using FIHC, imaged using confocal microscopy and analyzed using a multichannel colocalization analysis. The areas of colocalization were used to generate an INV score. Using the INV score, we were able to identify progressing lesions with a sensitivity of 75–100% and specificity of 72–76%. A positive INV score was associated with increased risk of progression to OSCC. Our results suggest that INV markers can be used in conjunction with the current diagnostic standard for early detection of OSCC. |
format | Online Article Text |
id | pubmed-7737762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77377622020-12-18 Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation Ali, Aiman Soares, Andresa Borges Eymael, Denise Magalhaes, Marco J Pathol Clin Res Original Articles Oral squamous cell carcinoma (OSCC) is the most common malignant tumor of the oral cavity and is usually preceded by a range of premalignant tissue abnormalities termed oral potentially malignant disorders. Identifying malignant transformation is critical for early treatment and consequently improved survival and decreased morbidity. Invadopodia (INV) are specialized subcellular structures required for cancer cell invasion. We developed a new method to visualize INV in keratinocytes using fluorescent immunohistochemistry (FIHC) and semi‐automated images analysis. The presence of INV was used to determine the risk of malignant transformation. We analyzed 145 formalin‐fixed, paraffin‐embedded (FFPE) oral biopsy samples from 95 patients diagnosed as nondysplastic, dysplastic, and OSCC including 49 patients whose lesions transformed to OSCC (progressing) and 46 cases that did not transform to OSCC (control). All samples were stained for Cortactin, tyrosine kinase substrate with five SH3 domains (Tks5) and matrix metallopeptidase 14 (MMP14) using FIHC, imaged using confocal microscopy and analyzed using a multichannel colocalization analysis. The areas of colocalization were used to generate an INV score. Using the INV score, we were able to identify progressing lesions with a sensitivity of 75–100% and specificity of 72–76%. A positive INV score was associated with increased risk of progression to OSCC. Our results suggest that INV markers can be used in conjunction with the current diagnostic standard for early detection of OSCC. John Wiley & Sons, Inc. 2020-10-01 /pmc/articles/PMC7737762/ /pubmed/33001588 http://dx.doi.org/10.1002/cjp2.182 Text en © 2020 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland & John Wiley & Sons, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Ali, Aiman Soares, Andresa Borges Eymael, Denise Magalhaes, Marco Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
title | Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
title_full | Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
title_fullStr | Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
title_full_unstemmed | Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
title_short | Expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
title_sort | expression of invadopodia markers can identify oral lesions with a high risk of malignant transformation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737762/ https://www.ncbi.nlm.nih.gov/pubmed/33001588 http://dx.doi.org/10.1002/cjp2.182 |
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