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Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review

Zoledronic acid (ZA) is one of the most important and effective class of anti-resorptive drug available among bisphosphonate (BP), which could effectively reduce the risk of skeletal-related events, and lead to a treatment paradigm for patients with skeletal involvement from advanced cancers. Howeve...

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Autores principales: Wang, Lianwei, Fang, Dengyang, Xu, Jinming, Luo, Runlan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607850/
https://www.ncbi.nlm.nih.gov/pubmed/33143662
http://dx.doi.org/10.1186/s12885-020-07568-9
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author Wang, Lianwei
Fang, Dengyang
Xu, Jinming
Luo, Runlan
author_facet Wang, Lianwei
Fang, Dengyang
Xu, Jinming
Luo, Runlan
author_sort Wang, Lianwei
collection PubMed
description Zoledronic acid (ZA) is one of the most important and effective class of anti-resorptive drug available among bisphosphonate (BP), which could effectively reduce the risk of skeletal-related events, and lead to a treatment paradigm for patients with skeletal involvement from advanced cancers. However, the exact molecular mechanisms of its anticancer effects have only recently been identified. In this review, we elaborate the detail mechanisms of ZA through inhibiting osteoclasts and cancer cells, which include the inhibition of differentiation of osteoclasts via suppressing receptor activator of nuclear factor κB ligand (RANKL)/receptor activator of nuclear factor κB (RANK) pathway, non-canonical Wnt/Ca2+/calmodulin dependent protein kinase II (CaMKII) pathway, and preventing of macrophage differentiation into osteoclasts, in addition, induction of apoptosis of osteoclasts through inhibiting farnesyl pyrophosphate synthase (FPPS)-mediated mevalonate pathway, and activation of reactive oxygen species (ROS)-induced pathway. Furthermore, ZA also inhibits cancer cells proliferation, viability, motility, invasion and angiogenesis; induces cancer cell apoptosis; reverts chemoresistance and stimulates immune response; and acts in synergy with other anti-cancer drugs. In addition, some new ways for delivering ZA against cancer is introduced. We hope this review will provide more information in support of future studies of ZA in the treatment of cancers and bone cancer metastasis.
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spelling pubmed-76078502020-11-03 Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review Wang, Lianwei Fang, Dengyang Xu, Jinming Luo, Runlan BMC Cancer Review Zoledronic acid (ZA) is one of the most important and effective class of anti-resorptive drug available among bisphosphonate (BP), which could effectively reduce the risk of skeletal-related events, and lead to a treatment paradigm for patients with skeletal involvement from advanced cancers. However, the exact molecular mechanisms of its anticancer effects have only recently been identified. In this review, we elaborate the detail mechanisms of ZA through inhibiting osteoclasts and cancer cells, which include the inhibition of differentiation of osteoclasts via suppressing receptor activator of nuclear factor κB ligand (RANKL)/receptor activator of nuclear factor κB (RANK) pathway, non-canonical Wnt/Ca2+/calmodulin dependent protein kinase II (CaMKII) pathway, and preventing of macrophage differentiation into osteoclasts, in addition, induction of apoptosis of osteoclasts through inhibiting farnesyl pyrophosphate synthase (FPPS)-mediated mevalonate pathway, and activation of reactive oxygen species (ROS)-induced pathway. Furthermore, ZA also inhibits cancer cells proliferation, viability, motility, invasion and angiogenesis; induces cancer cell apoptosis; reverts chemoresistance and stimulates immune response; and acts in synergy with other anti-cancer drugs. In addition, some new ways for delivering ZA against cancer is introduced. We hope this review will provide more information in support of future studies of ZA in the treatment of cancers and bone cancer metastasis. BioMed Central 2020-11-03 /pmc/articles/PMC7607850/ /pubmed/33143662 http://dx.doi.org/10.1186/s12885-020-07568-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Wang, Lianwei
Fang, Dengyang
Xu, Jinming
Luo, Runlan
Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
title Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
title_full Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
title_fullStr Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
title_full_unstemmed Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
title_short Various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
title_sort various pathways of zoledronic acid against osteoclasts and bone cancer metastasis: a brief review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607850/
https://www.ncbi.nlm.nih.gov/pubmed/33143662
http://dx.doi.org/10.1186/s12885-020-07568-9
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