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Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis

Prostate cancer (PCa) is one of the most prevalent and malignant cancer types in men, which causes more than three-hundred thousand cancer death each year. At late stage of PCa progression, bone marrow is the most often metastatic site that constitutes almost 70% of metastatic cases of the PCa popul...

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Autores principales: Lin, Shian-Ren, Mokgautsi, Ntlotlang, Liu, Yen-Nien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287876/
https://www.ncbi.nlm.nih.gov/pubmed/32443915
http://dx.doi.org/10.3390/molecules25102380
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author Lin, Shian-Ren
Mokgautsi, Ntlotlang
Liu, Yen-Nien
author_facet Lin, Shian-Ren
Mokgautsi, Ntlotlang
Liu, Yen-Nien
author_sort Lin, Shian-Ren
collection PubMed
description Prostate cancer (PCa) is one of the most prevalent and malignant cancer types in men, which causes more than three-hundred thousand cancer death each year. At late stage of PCa progression, bone marrow is the most often metastatic site that constitutes almost 70% of metastatic cases of the PCa population. However, the characteristic for the osteo-philic property of PCa is still puzzling. Recent studies reported that the Wnt and Ras signaling pathways are pivotal in bone metastasis and that take parts in different cytological changes, but their crosstalk is not well studied. In this review, we focused on interactions between the Wnt and Ras signaling pathways during each stage of bone metastasis and present the fate of those interactions. This review contributes insights that can guide other researchers by unveiling more details with regard to bone metastasis and might also help in finding potential therapeutic regimens for preventing PCa bone metastasis.
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spelling pubmed-72878762020-06-15 Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis Lin, Shian-Ren Mokgautsi, Ntlotlang Liu, Yen-Nien Molecules Review Prostate cancer (PCa) is one of the most prevalent and malignant cancer types in men, which causes more than three-hundred thousand cancer death each year. At late stage of PCa progression, bone marrow is the most often metastatic site that constitutes almost 70% of metastatic cases of the PCa population. However, the characteristic for the osteo-philic property of PCa is still puzzling. Recent studies reported that the Wnt and Ras signaling pathways are pivotal in bone metastasis and that take parts in different cytological changes, but their crosstalk is not well studied. In this review, we focused on interactions between the Wnt and Ras signaling pathways during each stage of bone metastasis and present the fate of those interactions. This review contributes insights that can guide other researchers by unveiling more details with regard to bone metastasis and might also help in finding potential therapeutic regimens for preventing PCa bone metastasis. MDPI 2020-05-20 /pmc/articles/PMC7287876/ /pubmed/32443915 http://dx.doi.org/10.3390/molecules25102380 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 Review
Lin, Shian-Ren
Mokgautsi, Ntlotlang
Liu, Yen-Nien
Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis
title Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis
title_full Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis
title_fullStr Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis
title_full_unstemmed Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis
title_short Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis
title_sort ras and wnt interaction contribute in prostate cancer bone metastasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287876/
https://www.ncbi.nlm.nih.gov/pubmed/32443915
http://dx.doi.org/10.3390/molecules25102380
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