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Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors

Proteasome inhibitors (PIs) can preferentially restore bone in bone-defective lesions of patients with multiple myeloma (MM) who respond favorably to these drugs. Most prior in vitro studies on PIs used continuous exposure to low PI concentrations, although pharmacokinetic analysis in patients has s...

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Autores principales: Nakaue, Emiko, Teramachi, Jumpei, Tenshin, Hirofumi, Hiasa, Masahiro, Harada, Takeshi, Oda, Asuka, Inoue, Yusuke, Shimizu, So, Higa, Yoshiki, Sogabe, Kimiko, Oura, Masahiro, Hara, Tomoyo, Sumitani, Ryohei, Maruhashi, Tomoko, Yamagami, Hiroki, Endo, Itsuro, Tanaka, Eiji, Abe, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284934/
https://www.ncbi.nlm.nih.gov/pubmed/37039914
http://dx.doi.org/10.1007/s12185-023-03601-2
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author Nakaue, Emiko
Teramachi, Jumpei
Tenshin, Hirofumi
Hiasa, Masahiro
Harada, Takeshi
Oda, Asuka
Inoue, Yusuke
Shimizu, So
Higa, Yoshiki
Sogabe, Kimiko
Oura, Masahiro
Hara, Tomoyo
Sumitani, Ryohei
Maruhashi, Tomoko
Yamagami, Hiroki
Endo, Itsuro
Tanaka, Eiji
Abe, Masahiro
author_facet Nakaue, Emiko
Teramachi, Jumpei
Tenshin, Hirofumi
Hiasa, Masahiro
Harada, Takeshi
Oda, Asuka
Inoue, Yusuke
Shimizu, So
Higa, Yoshiki
Sogabe, Kimiko
Oura, Masahiro
Hara, Tomoyo
Sumitani, Ryohei
Maruhashi, Tomoko
Yamagami, Hiroki
Endo, Itsuro
Tanaka, Eiji
Abe, Masahiro
author_sort Nakaue, Emiko
collection PubMed
description Proteasome inhibitors (PIs) can preferentially restore bone in bone-defective lesions of patients with multiple myeloma (MM) who respond favorably to these drugs. Most prior in vitro studies on PIs used continuous exposure to low PI concentrations, although pharmacokinetic analysis in patients has shown that serum concentrations of PIs change in a pulsatile manner. In the present study, we explored the effects of pulsatile treatment with PIs on bone metabolism to simulate in vivo PI pharmacokinetics. Pulsatile treatment with bortezomib, carfilzomib, or ixazomib induced MM cell death but only marginally affected the viability of osteoclasts (OCs) with F-actin ring formation. Pulsatile PI treatment suppressed osteoclastogenesis in OC precursors and bone resorption by mature OCs. OCs robustly enhanced osteoblastogenesis in cocultures with OCs and MC3T3-E1 pre-osteoblastic cells, indicating OC-mediated coupling to osteoblastogenesis. Importantly, pulsatile PI treatment did not impair robust OC-mediated osteoblastogenesis. These results suggest that PIs might sufficiently reduce MM cell-derived osteoblastogenesis inhibitors to permit OC-driven bone formation coupling while suppressing OC differentiation and activity in good responders to PIs. OC-mediated coupling to osteoblastogenesis appears to be a predominant mechanism for preferential occurrence of bone regeneration at sites of osteoclastic bone destruction in good responders.
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spelling pubmed-102849342023-06-23 Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors Nakaue, Emiko Teramachi, Jumpei Tenshin, Hirofumi Hiasa, Masahiro Harada, Takeshi Oda, Asuka Inoue, Yusuke Shimizu, So Higa, Yoshiki Sogabe, Kimiko Oura, Masahiro Hara, Tomoyo Sumitani, Ryohei Maruhashi, Tomoko Yamagami, Hiroki Endo, Itsuro Tanaka, Eiji Abe, Masahiro Int J Hematol Original Article Proteasome inhibitors (PIs) can preferentially restore bone in bone-defective lesions of patients with multiple myeloma (MM) who respond favorably to these drugs. Most prior in vitro studies on PIs used continuous exposure to low PI concentrations, although pharmacokinetic analysis in patients has shown that serum concentrations of PIs change in a pulsatile manner. In the present study, we explored the effects of pulsatile treatment with PIs on bone metabolism to simulate in vivo PI pharmacokinetics. Pulsatile treatment with bortezomib, carfilzomib, or ixazomib induced MM cell death but only marginally affected the viability of osteoclasts (OCs) with F-actin ring formation. Pulsatile PI treatment suppressed osteoclastogenesis in OC precursors and bone resorption by mature OCs. OCs robustly enhanced osteoblastogenesis in cocultures with OCs and MC3T3-E1 pre-osteoblastic cells, indicating OC-mediated coupling to osteoblastogenesis. Importantly, pulsatile PI treatment did not impair robust OC-mediated osteoblastogenesis. These results suggest that PIs might sufficiently reduce MM cell-derived osteoblastogenesis inhibitors to permit OC-driven bone formation coupling while suppressing OC differentiation and activity in good responders to PIs. OC-mediated coupling to osteoblastogenesis appears to be a predominant mechanism for preferential occurrence of bone regeneration at sites of osteoclastic bone destruction in good responders. Springer Nature Singapore 2023-04-11 2023 /pmc/articles/PMC10284934/ /pubmed/37039914 http://dx.doi.org/10.1007/s12185-023-03601-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Nakaue, Emiko
Teramachi, Jumpei
Tenshin, Hirofumi
Hiasa, Masahiro
Harada, Takeshi
Oda, Asuka
Inoue, Yusuke
Shimizu, So
Higa, Yoshiki
Sogabe, Kimiko
Oura, Masahiro
Hara, Tomoyo
Sumitani, Ryohei
Maruhashi, Tomoko
Yamagami, Hiroki
Endo, Itsuro
Tanaka, Eiji
Abe, Masahiro
Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
title Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
title_full Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
title_fullStr Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
title_full_unstemmed Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
title_short Mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
title_sort mechanisms of preferential bone formation in myeloma bone lesions by proteasome inhibitors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284934/
https://www.ncbi.nlm.nih.gov/pubmed/37039914
http://dx.doi.org/10.1007/s12185-023-03601-2
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