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Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel
BACKGROUND: Promoter methylation has emerged as a promising class of epigenetic biomarkers for diagnosis and prognosis of renal cell tumors (RCTs). Although differential gene promoter methylation patterns have been reported for the major subtypes (clear cell, papillary and chromophobe renal cell car...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492907/ https://www.ncbi.nlm.nih.gov/pubmed/28662726 http://dx.doi.org/10.1186/s12967-017-1248-y |
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author | Pires-Luís, Ana Sílvia Costa-Pinheiro, Pedro Ferreira, Maria João Antunes, Luís Lobo, Francisco Oliveira, Jorge Henrique, Rui Jerónimo, Carmen |
author_facet | Pires-Luís, Ana Sílvia Costa-Pinheiro, Pedro Ferreira, Maria João Antunes, Luís Lobo, Francisco Oliveira, Jorge Henrique, Rui Jerónimo, Carmen |
author_sort | Pires-Luís, Ana Sílvia |
collection | PubMed |
description | BACKGROUND: Promoter methylation has emerged as a promising class of epigenetic biomarkers for diagnosis and prognosis of renal cell tumors (RCTs). Although differential gene promoter methylation patterns have been reported for the major subtypes (clear cell, papillary and chromophobe renal cell carcinoma, and oncocytoma), validation of diagnostic performance in independent series have been seldom performed. Herein, we aimed at assessing the diagnostic performance of genes previously shown to be hypermethylated in RCTs in different clinical settings. METHODS: Promoter methylation levels of HOXA9 and OXR1 were assessed by quantitative methylation specific PCR. ROC curves were generated for OXR1, OXR1 combined with MST1R and HOXA9. Sensitivity, specificity, positive predictive value, negative predictive value and accuracy were computed, maximizing specificity. Methylation levels were also correlated with clinical and pathological relevant parameters. RESULTS: HOXA9 and OXR1 promoter methylation was disclosed in 73 and 87% of RCTs, respectively. A two-gene methylation panel comprising OXR1 and MST1R identified malignancy with 98% sensitivity and 100% specificity, and clear cell renal cell carcinoma with 90% sensitivity and 98% specificity. HOXA9 promoter methylation allowed for discrimination between oncocytoma and both papillary and chromophobe renal cell carcinoma but only with 77% sensitivity and 73% specificity. Significantly higher OXR1 promoter methylation levels (p = 0.005) were associated with high nuclear grade in ccRCC. CONCLUSIONS: A panel including OXR1 and MST1R promoter methylation allows specific and sensitive identification of renal cell tumors, and, especially, of clear cell renal cell carcinoma. Moreover, higher OXR1 promoter methylation levels associate with clear cell renal cell carcinoma nuclear grade, a surrogate for tumor aggressiveness. Thus, gene promoter methylation analysis might a useful ancillary tool in diagnostic management of renal masses. |
format | Online Article Text |
id | pubmed-5492907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54929072017-06-30 Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel Pires-Luís, Ana Sílvia Costa-Pinheiro, Pedro Ferreira, Maria João Antunes, Luís Lobo, Francisco Oliveira, Jorge Henrique, Rui Jerónimo, Carmen J Transl Med Research BACKGROUND: Promoter methylation has emerged as a promising class of epigenetic biomarkers for diagnosis and prognosis of renal cell tumors (RCTs). Although differential gene promoter methylation patterns have been reported for the major subtypes (clear cell, papillary and chromophobe renal cell carcinoma, and oncocytoma), validation of diagnostic performance in independent series have been seldom performed. Herein, we aimed at assessing the diagnostic performance of genes previously shown to be hypermethylated in RCTs in different clinical settings. METHODS: Promoter methylation levels of HOXA9 and OXR1 were assessed by quantitative methylation specific PCR. ROC curves were generated for OXR1, OXR1 combined with MST1R and HOXA9. Sensitivity, specificity, positive predictive value, negative predictive value and accuracy were computed, maximizing specificity. Methylation levels were also correlated with clinical and pathological relevant parameters. RESULTS: HOXA9 and OXR1 promoter methylation was disclosed in 73 and 87% of RCTs, respectively. A two-gene methylation panel comprising OXR1 and MST1R identified malignancy with 98% sensitivity and 100% specificity, and clear cell renal cell carcinoma with 90% sensitivity and 98% specificity. HOXA9 promoter methylation allowed for discrimination between oncocytoma and both papillary and chromophobe renal cell carcinoma but only with 77% sensitivity and 73% specificity. Significantly higher OXR1 promoter methylation levels (p = 0.005) were associated with high nuclear grade in ccRCC. CONCLUSIONS: A panel including OXR1 and MST1R promoter methylation allows specific and sensitive identification of renal cell tumors, and, especially, of clear cell renal cell carcinoma. Moreover, higher OXR1 promoter methylation levels associate with clear cell renal cell carcinoma nuclear grade, a surrogate for tumor aggressiveness. Thus, gene promoter methylation analysis might a useful ancillary tool in diagnostic management of renal masses. BioMed Central 2017-06-29 /pmc/articles/PMC5492907/ /pubmed/28662726 http://dx.doi.org/10.1186/s12967-017-1248-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Pires-Luís, Ana Sílvia Costa-Pinheiro, Pedro Ferreira, Maria João Antunes, Luís Lobo, Francisco Oliveira, Jorge Henrique, Rui Jerónimo, Carmen Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
title | Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
title_full | Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
title_fullStr | Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
title_full_unstemmed | Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
title_short | Identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
title_sort | identification of clear cell renal cell carcinoma and oncocytoma using a three-gene promoter methylation panel |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492907/ https://www.ncbi.nlm.nih.gov/pubmed/28662726 http://dx.doi.org/10.1186/s12967-017-1248-y |
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