Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel
Background: androgen deprivation therapy (ADT) and docetaxel (DX) combination is a standard therapy for metastatic hormone-sensitive prostate cancer (mHSPC) patients. (2) Methods: We investigate if tumor transcriptomic analysis predicts mHSPC evolution in a multicenter retrospective biomarker study....
| Autores: | , , , , , , , , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2022 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10230/55438 |
| Acceso en línea: | http://hdl.handle.net/10230/55438 http://dx.doi.org/10.3390/cancers14194757 |
| Access Level: | acceso abierto |
| Palabra clave: | Androgen receptor Chemotherapy Estrogen receptor Hormonal therapy Metastatic prostate cancer Predictive biomarkers Tumor suppressor genes |
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Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxelJiménez, NataliaReig, ÒscarMarín-Aguilera, MercedesAversa, CaterinaFerrer-Mileo, LauraFont, AlbertRodriguez-Vida, AlejoCliment, Miguel ÁngelCros, SaraChirivella, IsabelDoménech, MontserratFigols, MarionaGonzález-Billalabeitia, EnriqueJiménez Peralta, DanielRodríguez-Carunchio, LeonardoGarcía-Esteve, SamuelGarcía de Herreros, MartaRibal, María JoséPrat, AleixMellado, BegoñaAndrogen receptorChemotherapyEstrogen receptorHormonal therapyMetastatic prostate cancerPredictive biomarkersTumor suppressor genesBackground: androgen deprivation therapy (ADT) and docetaxel (DX) combination is a standard therapy for metastatic hormone-sensitive prostate cancer (mHSPC) patients. (2) Methods: We investigate if tumor transcriptomic analysis predicts mHSPC evolution in a multicenter retrospective biomarker study. A customized panel of 184 genes was tested in mRNA from tumor samples by the nCounter platform in 125 mHSPC patients treated with ADT+DX. Gene expression was correlated with castration-resistant prostate cancer-free survival (CRPC-FS) and overall survival (OS). (3) Results: High expression of androgen receptor (AR) signature was independently associated with longer CRPC-FS (hazard ratio (HR) 0.6, 95% confidence interval (CI) 0.3-0.9; p = 0.015), high expression of estrogen receptor (ESR) signature with longer CRPC-FS (HR 0.6, 95% CI 0.4-0.9; p = 0.019) and OS (HR 0.5, 95% CI 0.2-0.9, p = 0.024), and lower expression of tumor suppressor genes (TSG) (RB1, PTEN and TP53) with shorter OS (HR 2, 95% CI 1-3.8; p = 0.044). ARV7 expression was independently associated with shorter CRPC-FS (HR 1.5, 95% CI 1.1-2.1, p = 0.008) and OS (HR 1.8, 95% CI 1.2-2.6, p = 0.004), high ESR2 was associated with longer OS (HR 0.5, 95% CI 0.2-1, p = 0.048) and low expression of RB1 was independently associated with shorter OS (HR 1.9, 95% CI 1.1-3.2, p = 0.014). (4) Conclusions: AR, ESR, and TSG expression signatures, as well as ARV7, RB1, and ESR2 expression, have a prognostic value in mHSPC patients treated with ADT+DX.MDPI202320232022info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/55438http://dx.doi.org/10.3390/cancers14194757reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésCopyright © 2022 by Jiménez N, Reig Ò, Marín-Aguilera M, Aversa C, Ferrer-Mileo L, Font A, et al. 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/).http://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10230/554382026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| title |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| spellingShingle |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel Jiménez, Natalia Androgen receptor Chemotherapy Estrogen receptor Hormonal therapy Metastatic prostate cancer Predictive biomarkers Tumor suppressor genes |
| title_short |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| title_full |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| title_fullStr |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| title_full_unstemmed |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| title_sort |
Transcriptional profile associated with clinical outcomes in metastatic hormone-sensitive prostate cancer treated with androgen deprivation and docetaxel |
| dc.creator.none.fl_str_mv |
Jiménez, Natalia Reig, Òscar Marín-Aguilera, Mercedes Aversa, Caterina Ferrer-Mileo, Laura Font, Albert Rodriguez-Vida, Alejo Climent, Miguel Ángel Cros, Sara Chirivella, Isabel Doménech, Montserrat Figols, Mariona González-Billalabeitia, Enrique Jiménez Peralta, Daniel Rodríguez-Carunchio, Leonardo García-Esteve, Samuel García de Herreros, Marta Ribal, María José Prat, Aleix Mellado, Begoña |
| author |
Jiménez, Natalia |
| author_facet |
Jiménez, Natalia Reig, Òscar Marín-Aguilera, Mercedes Aversa, Caterina Ferrer-Mileo, Laura Font, Albert Rodriguez-Vida, Alejo Climent, Miguel Ángel Cros, Sara Chirivella, Isabel Doménech, Montserrat Figols, Mariona González-Billalabeitia, Enrique Jiménez Peralta, Daniel Rodríguez-Carunchio, Leonardo García-Esteve, Samuel García de Herreros, Marta Ribal, María José Prat, Aleix Mellado, Begoña |
| author_role |
author |
| author2 |
Reig, Òscar Marín-Aguilera, Mercedes Aversa, Caterina Ferrer-Mileo, Laura Font, Albert Rodriguez-Vida, Alejo Climent, Miguel Ángel Cros, Sara Chirivella, Isabel Doménech, Montserrat Figols, Mariona González-Billalabeitia, Enrique Jiménez Peralta, Daniel Rodríguez-Carunchio, Leonardo García-Esteve, Samuel García de Herreros, Marta Ribal, María José Prat, Aleix Mellado, Begoña |
| author2_role |
author author author author author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Androgen receptor Chemotherapy Estrogen receptor Hormonal therapy Metastatic prostate cancer Predictive biomarkers Tumor suppressor genes |
| topic |
Androgen receptor Chemotherapy Estrogen receptor Hormonal therapy Metastatic prostate cancer Predictive biomarkers Tumor suppressor genes |
| description |
Background: androgen deprivation therapy (ADT) and docetaxel (DX) combination is a standard therapy for metastatic hormone-sensitive prostate cancer (mHSPC) patients. (2) Methods: We investigate if tumor transcriptomic analysis predicts mHSPC evolution in a multicenter retrospective biomarker study. A customized panel of 184 genes was tested in mRNA from tumor samples by the nCounter platform in 125 mHSPC patients treated with ADT+DX. Gene expression was correlated with castration-resistant prostate cancer-free survival (CRPC-FS) and overall survival (OS). (3) Results: High expression of androgen receptor (AR) signature was independently associated with longer CRPC-FS (hazard ratio (HR) 0.6, 95% confidence interval (CI) 0.3-0.9; p = 0.015), high expression of estrogen receptor (ESR) signature with longer CRPC-FS (HR 0.6, 95% CI 0.4-0.9; p = 0.019) and OS (HR 0.5, 95% CI 0.2-0.9, p = 0.024), and lower expression of tumor suppressor genes (TSG) (RB1, PTEN and TP53) with shorter OS (HR 2, 95% CI 1-3.8; p = 0.044). ARV7 expression was independently associated with shorter CRPC-FS (HR 1.5, 95% CI 1.1-2.1, p = 0.008) and OS (HR 1.8, 95% CI 1.2-2.6, p = 0.004), high ESR2 was associated with longer OS (HR 0.5, 95% CI 0.2-1, p = 0.048) and low expression of RB1 was independently associated with shorter OS (HR 1.9, 95% CI 1.1-3.2, p = 0.014). (4) Conclusions: AR, ESR, and TSG expression signatures, as well as ARV7, RB1, and ESR2 expression, have a prognostic value in mHSPC patients treated with ADT+DX. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2022 2023 2023 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10230/55438 http://dx.doi.org/10.3390/cancers14194757 |
| url |
http://hdl.handle.net/10230/55438 http://dx.doi.org/10.3390/cancers14194757 |
| dc.language.none.fl_str_mv |
Inglés |
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Inglés |
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http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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application/pdf application/pdf |
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MDPI |
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MDPI |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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