Cargando…

Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway

More than 50% of prostate cancer (PCa) patients have bone metastasis with osteoblastic lesions. MiR-18a-5p is associated with the development and metastasis of PCa, but it remains unclear whether it is involved in osteoblastic lesions. We first found that miR-18a-5p was highly expressed in the bone...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Fanchun, Zhao, Chunrong, Wang, Rujie, Ren, Lingyan, Qiu, Hao, Zou, Zhi, Ding, Haibin, Sun, Zhongyi, Li, Jianmei, Dong, Shiwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311030/
https://www.ncbi.nlm.nih.gov/pubmed/37397518
http://dx.doi.org/10.1016/j.gendis.2022.06.007
_version_ 1785066658208940032
author Zeng, Fanchun
Zhao, Chunrong
Wang, Rujie
Ren, Lingyan
Qiu, Hao
Zou, Zhi
Ding, Haibin
Sun, Zhongyi
Li, Jianmei
Dong, Shiwu
author_facet Zeng, Fanchun
Zhao, Chunrong
Wang, Rujie
Ren, Lingyan
Qiu, Hao
Zou, Zhi
Ding, Haibin
Sun, Zhongyi
Li, Jianmei
Dong, Shiwu
author_sort Zeng, Fanchun
collection PubMed
description More than 50% of prostate cancer (PCa) patients have bone metastasis with osteoblastic lesions. MiR-18a-5p is associated with the development and metastasis of PCa, but it remains unclear whether it is involved in osteoblastic lesions. We first found that miR-18a-5p was highly expressed in the bone microenvironment of patients with PCa bone metastases. To address how miR-18a-5p affects PCa osteoblastic lesions, antagonizing miR-18a-5p in PCa cells or pre-osteoblasts inhibited osteoblast differentiation in vitro. Moreover, injection of PCa cells with miR-18a-5p inhibition improved bone biomechanical properties and bone mineral mass in vivo. Furthermore, miR-18a-5p was transferred to osteoblasts by exosomes derived from PCa cells and targeted the Hist1h2bc gene, resulting in Ctnnb1 up-regulation in the Wnt/β-catenin signaling pathway. Translationally, antagomir-18a-5p significantly improved bone biomechanical properties and alleviated sclerotic lesions from osteoblastic metastases in BALB/c nude mice. These data suggest that inhibition of exosome-delivered miR-18a-5p ameliorates PCa-induced osteoblastic lesions.
format Online
Article
Text
id pubmed-10311030
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Chongqing Medical University
record_format MEDLINE/PubMed
spelling pubmed-103110302023-07-01 Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway Zeng, Fanchun Zhao, Chunrong Wang, Rujie Ren, Lingyan Qiu, Hao Zou, Zhi Ding, Haibin Sun, Zhongyi Li, Jianmei Dong, Shiwu Genes Dis Full Length Article More than 50% of prostate cancer (PCa) patients have bone metastasis with osteoblastic lesions. MiR-18a-5p is associated with the development and metastasis of PCa, but it remains unclear whether it is involved in osteoblastic lesions. We first found that miR-18a-5p was highly expressed in the bone microenvironment of patients with PCa bone metastases. To address how miR-18a-5p affects PCa osteoblastic lesions, antagonizing miR-18a-5p in PCa cells or pre-osteoblasts inhibited osteoblast differentiation in vitro. Moreover, injection of PCa cells with miR-18a-5p inhibition improved bone biomechanical properties and bone mineral mass in vivo. Furthermore, miR-18a-5p was transferred to osteoblasts by exosomes derived from PCa cells and targeted the Hist1h2bc gene, resulting in Ctnnb1 up-regulation in the Wnt/β-catenin signaling pathway. Translationally, antagomir-18a-5p significantly improved bone biomechanical properties and alleviated sclerotic lesions from osteoblastic metastases in BALB/c nude mice. These data suggest that inhibition of exosome-delivered miR-18a-5p ameliorates PCa-induced osteoblastic lesions. Chongqing Medical University 2022-07-30 /pmc/articles/PMC10311030/ /pubmed/37397518 http://dx.doi.org/10.1016/j.gendis.2022.06.007 Text en © 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Zeng, Fanchun
Zhao, Chunrong
Wang, Rujie
Ren, Lingyan
Qiu, Hao
Zou, Zhi
Ding, Haibin
Sun, Zhongyi
Li, Jianmei
Dong, Shiwu
Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway
title Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway
title_full Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway
title_fullStr Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway
title_full_unstemmed Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway
title_short Antagonizing exosomal miR-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting Hist1h2bc and activating Wnt/β-catenin pathway
title_sort antagonizing exosomal mir-18a-5p derived from prostate cancer cells ameliorates metastasis-induced osteoblastic lesions by targeting hist1h2bc and activating wnt/β-catenin pathway
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311030/
https://www.ncbi.nlm.nih.gov/pubmed/37397518
http://dx.doi.org/10.1016/j.gendis.2022.06.007
work_keys_str_mv AT zengfanchun antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT zhaochunrong antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT wangrujie antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT renlingyan antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT qiuhao antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT zouzhi antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT dinghaibin antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT sunzhongyi antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT lijianmei antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway
AT dongshiwu antagonizingexosomalmir18a5pderivedfromprostatecancercellsamelioratesmetastasisinducedosteoblasticlesionsbytargetinghist1h2bcandactivatingwntbcateninpathway