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BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis
The etiology of endometriosis is highly complex, and although it is a benign disease, it has several biological behaviors similar to malignant lesions, including cell invasion, neo-angiogenesis, and decreased apoptosis. Survivin is a protein encoded by the BIRC5 gene that plays a role in cell divisi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459871/ https://www.ncbi.nlm.nih.gov/pubmed/32751449 http://dx.doi.org/10.3390/diagnostics10080533 |
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author | Filipchiuk, Carolina Laganà, Antonio Simone Beteli, Rubia Ponce, Tatiana Guida Christofolini, Denise Maria Martins Trevisan, Camila Fonseca, Fernando Luiz Affonso Barbosa, Caio Parente Bianco, Bianca |
author_facet | Filipchiuk, Carolina Laganà, Antonio Simone Beteli, Rubia Ponce, Tatiana Guida Christofolini, Denise Maria Martins Trevisan, Camila Fonseca, Fernando Luiz Affonso Barbosa, Caio Parente Bianco, Bianca |
author_sort | Filipchiuk, Carolina |
collection | PubMed |
description | The etiology of endometriosis is highly complex, and although it is a benign disease, it has several biological behaviors similar to malignant lesions, including cell invasion, neo-angiogenesis, and decreased apoptosis. Survivin is a protein encoded by the BIRC5 gene that plays a role in cell division by inhibiting apoptosis and regulating the process of mitosis in embryonic and cancer cells. Therefore, we aimed to evaluate the expression of BIRC5 in samples of peripheral blood of women with and without endometriosis. This study comprised of 40 women with endometriosis and 10 healthy women as controls. Peripheral blood samples were collected in the three phases of the menstrual cycle (follicular, ovulatory, and luteal). The expression of the BIRC5 gene was evaluated by RT-qPCR using the TaqMan methodology. The BIRC5 expression was significantly higher in all phases of the menstrual cycle in women with endometriosis, regardless of the disease stage. The accuracy of BIRC5 expression in the peripheral blood for the diagnosis endometriosis presented AUC of 0.887 (p < 0.001), with 97.2% of sensitivity and specificity of 65.5% considering the overall endometriosis group. Regarding the minimal/mild endometriosis group, the AUC presented a value of 0.925 (p < 0.001), with 100% of sensitivity and 79.3% of specificity, whereas in the moderate/severe endometriosis group the AUC was 0.868 (p < 0.001), with a sensitivity of 95.8% and specificity of 65.5%. These findings suggest that the expression of BIRC5 may be a potential noninvasive biomarker for the diagnosis of endometriosis. |
format | Online Article Text |
id | pubmed-7459871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74598712020-09-02 BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis Filipchiuk, Carolina Laganà, Antonio Simone Beteli, Rubia Ponce, Tatiana Guida Christofolini, Denise Maria Martins Trevisan, Camila Fonseca, Fernando Luiz Affonso Barbosa, Caio Parente Bianco, Bianca Diagnostics (Basel) Article The etiology of endometriosis is highly complex, and although it is a benign disease, it has several biological behaviors similar to malignant lesions, including cell invasion, neo-angiogenesis, and decreased apoptosis. Survivin is a protein encoded by the BIRC5 gene that plays a role in cell division by inhibiting apoptosis and regulating the process of mitosis in embryonic and cancer cells. Therefore, we aimed to evaluate the expression of BIRC5 in samples of peripheral blood of women with and without endometriosis. This study comprised of 40 women with endometriosis and 10 healthy women as controls. Peripheral blood samples were collected in the three phases of the menstrual cycle (follicular, ovulatory, and luteal). The expression of the BIRC5 gene was evaluated by RT-qPCR using the TaqMan methodology. The BIRC5 expression was significantly higher in all phases of the menstrual cycle in women with endometriosis, regardless of the disease stage. The accuracy of BIRC5 expression in the peripheral blood for the diagnosis endometriosis presented AUC of 0.887 (p < 0.001), with 97.2% of sensitivity and specificity of 65.5% considering the overall endometriosis group. Regarding the minimal/mild endometriosis group, the AUC presented a value of 0.925 (p < 0.001), with 100% of sensitivity and 79.3% of specificity, whereas in the moderate/severe endometriosis group the AUC was 0.868 (p < 0.001), with a sensitivity of 95.8% and specificity of 65.5%. These findings suggest that the expression of BIRC5 may be a potential noninvasive biomarker for the diagnosis of endometriosis. MDPI 2020-07-30 /pmc/articles/PMC7459871/ /pubmed/32751449 http://dx.doi.org/10.3390/diagnostics10080533 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Filipchiuk, Carolina Laganà, Antonio Simone Beteli, Rubia Ponce, Tatiana Guida Christofolini, Denise Maria Martins Trevisan, Camila Fonseca, Fernando Luiz Affonso Barbosa, Caio Parente Bianco, Bianca BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis |
title | BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis |
title_full | BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis |
title_fullStr | BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis |
title_full_unstemmed | BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis |
title_short | BIRC5/Survivin Expression as a Non-Invasive Biomarker of Endometriosis |
title_sort | birc5/survivin expression as a non-invasive biomarker of endometriosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459871/ https://www.ncbi.nlm.nih.gov/pubmed/32751449 http://dx.doi.org/10.3390/diagnostics10080533 |
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