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Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow

Prostate cancer (PCa) continues to be the most common, noncutaneous cancer in men. Bone is the most frequent site of PCa metastases, and up to 90% of patients with advanced PCa develop bone metastases. An altered bone marrow microenvironment, induced by obesity, is a significant mediator for the bon...

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Autores principales: Wang, Cuizhe, Wang, Jingzhou, Chen, Keru, Pang, Huai, Li, Xue, Zhu, Jiaojiao, Ma, Yinghua, Qiu, Tongtong, Li, Wei, Xie, Jianxin, Zhang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540990/
https://www.ncbi.nlm.nih.gov/pubmed/32770813
http://dx.doi.org/10.1111/cas.14606
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author Wang, Cuizhe
Wang, Jingzhou
Chen, Keru
Pang, Huai
Li, Xue
Zhu, Jiaojiao
Ma, Yinghua
Qiu, Tongtong
Li, Wei
Xie, Jianxin
Zhang, Jun
author_facet Wang, Cuizhe
Wang, Jingzhou
Chen, Keru
Pang, Huai
Li, Xue
Zhu, Jiaojiao
Ma, Yinghua
Qiu, Tongtong
Li, Wei
Xie, Jianxin
Zhang, Jun
author_sort Wang, Cuizhe
collection PubMed
description Prostate cancer (PCa) continues to be the most common, noncutaneous cancer in men. Bone is the most frequent site of PCa metastases, and up to 90% of patients with advanced PCa develop bone metastases. An altered bone marrow microenvironment, induced by obesity, is a significant mediator for the bone tropism of PCa. However, the specific molecular mechanisms by which obesity causes changes in the bone marrow microenvironment, leading to PCa bone metastasis, are not fully understood. Our results demonstrate that a high‐fat diet (HFD) leads to dyslipidemia and changes in bone marrow of nude mice: an increase in the area and number of adipocytes and a reduction in the area and number of osteoblasts. Moreover, a HFD promoted cyclooxygenase 2 (COX2) expression and inhibited osteoprotegerin (OPG) expression in the bone microenvironment. Additionally, the total level of free fatty acids (FFAs) and caprylic acid (C8:0) was significantly higher in PCa patients with bone metastases. In vitro, caprylic acid (C8:0) promoted bone mesenchymal stem cell (MSC)‐derived adipocytic differentiation, COX2 expression, and prostaglandin E2 (PGE2) secretion, whereas osteoblastic differentiation and OPG expression were reduced. Furthermore, caprylic acid (C8:0)‐treated adipocytes promoted the invasion and migration of PCa cells. Taken together, our findings suggest caprylic acid (C8:0) promotes bone metastasis of PCa by dysregulated adipo‐osteogenic balance of bone marrow.
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spelling pubmed-75409902020-10-09 Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow Wang, Cuizhe Wang, Jingzhou Chen, Keru Pang, Huai Li, Xue Zhu, Jiaojiao Ma, Yinghua Qiu, Tongtong Li, Wei Xie, Jianxin Zhang, Jun Cancer Sci Carcinogenesis Prostate cancer (PCa) continues to be the most common, noncutaneous cancer in men. Bone is the most frequent site of PCa metastases, and up to 90% of patients with advanced PCa develop bone metastases. An altered bone marrow microenvironment, induced by obesity, is a significant mediator for the bone tropism of PCa. However, the specific molecular mechanisms by which obesity causes changes in the bone marrow microenvironment, leading to PCa bone metastasis, are not fully understood. Our results demonstrate that a high‐fat diet (HFD) leads to dyslipidemia and changes in bone marrow of nude mice: an increase in the area and number of adipocytes and a reduction in the area and number of osteoblasts. Moreover, a HFD promoted cyclooxygenase 2 (COX2) expression and inhibited osteoprotegerin (OPG) expression in the bone microenvironment. Additionally, the total level of free fatty acids (FFAs) and caprylic acid (C8:0) was significantly higher in PCa patients with bone metastases. In vitro, caprylic acid (C8:0) promoted bone mesenchymal stem cell (MSC)‐derived adipocytic differentiation, COX2 expression, and prostaglandin E2 (PGE2) secretion, whereas osteoblastic differentiation and OPG expression were reduced. Furthermore, caprylic acid (C8:0)‐treated adipocytes promoted the invasion and migration of PCa cells. Taken together, our findings suggest caprylic acid (C8:0) promotes bone metastasis of PCa by dysregulated adipo‐osteogenic balance of bone marrow. John Wiley and Sons Inc. 2020-08-28 2020-10 /pmc/articles/PMC7540990/ /pubmed/32770813 http://dx.doi.org/10.1111/cas.14606 Text en © 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Carcinogenesis
Wang, Cuizhe
Wang, Jingzhou
Chen, Keru
Pang, Huai
Li, Xue
Zhu, Jiaojiao
Ma, Yinghua
Qiu, Tongtong
Li, Wei
Xie, Jianxin
Zhang, Jun
Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
title Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
title_full Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
title_fullStr Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
title_full_unstemmed Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
title_short Caprylic acid (C8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
title_sort caprylic acid (c8:0) promotes bone metastasis of prostate cancer by dysregulated adipo‐osteogenic balance in bone marrow
topic Carcinogenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540990/
https://www.ncbi.nlm.nih.gov/pubmed/32770813
http://dx.doi.org/10.1111/cas.14606
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