Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside

Prostate cancer (PCa) is the second most frequent type of cancer in men worldwide, with 288,300 new cases and 34,700 deaths estimated in the United States in 2023. Treatment options for early-stage disease include external beam radiation therapy, brachytherapy, radical prostatectomy, active surveill...

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Main Authors: Samantha Gogola, Michael Rejzer, Hisham F. Bahmad, Wassim Abou-Kheir, Yumna Omarzai, Robert Poppiti
Format: Article
Language:English
Published: MDPI AG 2023-04-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/15/8/2309
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author Samantha Gogola
Michael Rejzer
Hisham F. Bahmad
Wassim Abou-Kheir
Yumna Omarzai
Robert Poppiti
author_facet Samantha Gogola
Michael Rejzer
Hisham F. Bahmad
Wassim Abou-Kheir
Yumna Omarzai
Robert Poppiti
author_sort Samantha Gogola
collection DOAJ
description Prostate cancer (PCa) is the second most frequent type of cancer in men worldwide, with 288,300 new cases and 34,700 deaths estimated in the United States in 2023. Treatment options for early-stage disease include external beam radiation therapy, brachytherapy, radical prostatectomy, active surveillance, or a combination of these. In advanced cases, androgen-deprivation therapy (ADT) is considered the first-line therapy; however, PCa in most patients eventually progresses to castration-resistant prostate cancer (CRPC) despite ADT. Nonetheless, the transition from androgen-dependent to androgen-independent tumors is not yet fully understood. The physiological processes of epithelial-to-non-epithelial (“mesenchymal”) transition (EMT) and mesenchymal-to-epithelial transition (MET) are essential for normal embryonic development; however, they have also been linked to higher tumor grade, metastatic progression, and treatment resistance. Due to this association, EMT and MET have been identified as important targets for novel cancer therapies, including CRPC. Here, we discuss the transcriptional factors and signaling pathways involved in EMT, in addition to the diagnostic and prognostic biomarkers that have been identified in these processes. We also tackle the various studies that have been conducted from bench to bedside and the current landscape of EMT-targeted therapies.
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spelling doaj.art-69a7cb1ef1fa4d7facab0973541996ad2023-11-17T18:39:11ZengMDPI AGCancers2072-66942023-04-01158230910.3390/cancers15082309Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to BedsideSamantha Gogola0Michael Rejzer1Hisham F. Bahmad2Wassim Abou-Kheir3Yumna Omarzai4Robert Poppiti5Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USAHerbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USAThe Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, FL 33140, USADepartment of Anatomy, Cell Biology and Physiological Sciences, Faculty of Medicine, American University of Beirut, Beirut 1107, LebanonThe Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, FL 33140, USAThe Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, FL 33140, USAProstate cancer (PCa) is the second most frequent type of cancer in men worldwide, with 288,300 new cases and 34,700 deaths estimated in the United States in 2023. Treatment options for early-stage disease include external beam radiation therapy, brachytherapy, radical prostatectomy, active surveillance, or a combination of these. In advanced cases, androgen-deprivation therapy (ADT) is considered the first-line therapy; however, PCa in most patients eventually progresses to castration-resistant prostate cancer (CRPC) despite ADT. Nonetheless, the transition from androgen-dependent to androgen-independent tumors is not yet fully understood. The physiological processes of epithelial-to-non-epithelial (“mesenchymal”) transition (EMT) and mesenchymal-to-epithelial transition (MET) are essential for normal embryonic development; however, they have also been linked to higher tumor grade, metastatic progression, and treatment resistance. Due to this association, EMT and MET have been identified as important targets for novel cancer therapies, including CRPC. Here, we discuss the transcriptional factors and signaling pathways involved in EMT, in addition to the diagnostic and prognostic biomarkers that have been identified in these processes. We also tackle the various studies that have been conducted from bench to bedside and the current landscape of EMT-targeted therapies.https://www.mdpi.com/2072-6694/15/8/2309prostate cancerepithelial-to-mesenchymal transitionmesenchymal-to-epithelial transitionEMTMETbiomarkers
spellingShingle Samantha Gogola
Michael Rejzer
Hisham F. Bahmad
Wassim Abou-Kheir
Yumna Omarzai
Robert Poppiti
Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside
Cancers
prostate cancer
epithelial-to-mesenchymal transition
mesenchymal-to-epithelial transition
EMT
MET
biomarkers
title Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside
title_full Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside
title_fullStr Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside
title_full_unstemmed Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside
title_short Epithelial-to-Mesenchymal Transition-Related Markers in Prostate Cancer: From Bench to Bedside
title_sort epithelial to mesenchymal transition related markers in prostate cancer from bench to bedside
topic prostate cancer
epithelial-to-mesenchymal transition
mesenchymal-to-epithelial transition
EMT
MET
biomarkers
url https://www.mdpi.com/2072-6694/15/8/2309
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