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Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors

Autocrine motility factor (AMF: GPI) and its receptor AMFR (AMF Receptor: gp78) regulate the metastatic process. Here, we have tested the expression levels of AMF, AMFR, and AMF × AMFR in 1348 patients with musculoskeletal tumor. The results depicted here identified that multiple myeloma highly expr...

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Autores principales: Nakajima, Kosei, Raz, Avraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378681/
https://www.ncbi.nlm.nih.gov/pubmed/32714781
http://dx.doi.org/10.1016/j.jbo.2020.100308
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author Nakajima, Kosei
Raz, Avraham
author_facet Nakajima, Kosei
Raz, Avraham
author_sort Nakajima, Kosei
collection PubMed
description Autocrine motility factor (AMF: GPI) and its receptor AMFR (AMF Receptor: gp78) regulate the metastatic process. Here, we have tested the expression levels of AMF, AMFR, and AMF × AMFR in 1348 patients with musculoskeletal tumor. The results depicted here identified that multiple myeloma highly express AMF × AMFR value as compared with normal bone samples (p < 0.00001). To visualize the AMF × AMFR autocrine amplification in multiple myeloma microenvironment, we have developed a novel software aimed at analyzing numerous cell-to-cell and ligand-to-receptor interactions, i.e., Environmentome. It has led to the identification that myeloma-associated interactions with normal bone cells including osteoblast, osteoclast, immunological components, and others in a paracrine manner. In conclusion, the data showed that AMF × AMFR amplification is a clinical manifestation in bone microenvironment of multiple myeloma.
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spelling pubmed-73786812020-07-24 Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors Nakajima, Kosei Raz, Avraham J Bone Oncol Research Article Autocrine motility factor (AMF: GPI) and its receptor AMFR (AMF Receptor: gp78) regulate the metastatic process. Here, we have tested the expression levels of AMF, AMFR, and AMF × AMFR in 1348 patients with musculoskeletal tumor. The results depicted here identified that multiple myeloma highly express AMF × AMFR value as compared with normal bone samples (p < 0.00001). To visualize the AMF × AMFR autocrine amplification in multiple myeloma microenvironment, we have developed a novel software aimed at analyzing numerous cell-to-cell and ligand-to-receptor interactions, i.e., Environmentome. It has led to the identification that myeloma-associated interactions with normal bone cells including osteoblast, osteoclast, immunological components, and others in a paracrine manner. In conclusion, the data showed that AMF × AMFR amplification is a clinical manifestation in bone microenvironment of multiple myeloma. Elsevier 2020-07-15 /pmc/articles/PMC7378681/ /pubmed/32714781 http://dx.doi.org/10.1016/j.jbo.2020.100308 Text en © 2020 The Author(s) http://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 Research Article
Nakajima, Kosei
Raz, Avraham
Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
title Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
title_full Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
title_fullStr Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
title_full_unstemmed Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
title_short Amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
title_sort amplification of autocrine motility factor and its receptor in multiple myeloma and other musculoskeletal tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378681/
https://www.ncbi.nlm.nih.gov/pubmed/32714781
http://dx.doi.org/10.1016/j.jbo.2020.100308
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