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The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma
SIMPLE SUMMARY: Multiple myeloma (MM) is the second most common hematological malignancy and remains incurable. Recent evidence substantiates the interaction of gut microbiota and MM, together with abnormal amino acid metabolism and MM. Moreover, the association between gut microbiota and host amino...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093363/ https://www.ncbi.nlm.nih.gov/pubmed/37046603 http://dx.doi.org/10.3390/cancers15071942 |
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author | Yang, Qin Wei, Yumou Zhu, Yinghong Guo, Jiaojiao Zhang, Jingyu He, Yanjuan Li, Xin Liu, Jing Zhou, Wen |
author_facet | Yang, Qin Wei, Yumou Zhu, Yinghong Guo, Jiaojiao Zhang, Jingyu He, Yanjuan Li, Xin Liu, Jing Zhou, Wen |
author_sort | Yang, Qin |
collection | PubMed |
description | SIMPLE SUMMARY: Multiple myeloma (MM) is the second most common hematological malignancy and remains incurable. Recent evidence substantiates the interaction of gut microbiota and MM, together with abnormal amino acid metabolism and MM. Moreover, the association between gut microbiota and host amino acid metabolism on MM has been highlighted. This article presents a review of the literature on the relationship between gut microbiota, metabolism, and MM, together with strategies to modulate the microbiota. ABSTRACT: Although novel therapies have dramatically improved outcomes for multiple myeloma (MM) patients, relapse is inevitable and overall outcomes are heterogeneous. The gut microbiota is becoming increasingly recognized for its influence on host metabolism. To date, evidence has suggested that the gut microbiota contributes to MM, not only via the progressive activities of specific bacteria but also through the influence of the microbiota on host metabolism. Importantly, the abnormal amino acid metabolism, as well as the altered microbiome in MM, is becoming increasingly apparent, as is the influence on MM progression and the therapeutic response. Moreover, the gut-microbiota–host-amino-acid metabolism interaction in the progression of MM has been highlighted. Modulation of the gut microbiota (such as fecal microbiota transplantation, FMT) can be modified, representing a new angle in MM treatment that can improve outcomes. In this review, the relationship between gut microbiota, metabolism, and MM, together with strategies to modulate the microbiota, will be discussed, and some unanswered questions for ongoing and future research will be presented. |
format | Online Article Text |
id | pubmed-10093363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100933632023-04-13 The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma Yang, Qin Wei, Yumou Zhu, Yinghong Guo, Jiaojiao Zhang, Jingyu He, Yanjuan Li, Xin Liu, Jing Zhou, Wen Cancers (Basel) Review SIMPLE SUMMARY: Multiple myeloma (MM) is the second most common hematological malignancy and remains incurable. Recent evidence substantiates the interaction of gut microbiota and MM, together with abnormal amino acid metabolism and MM. Moreover, the association between gut microbiota and host amino acid metabolism on MM has been highlighted. This article presents a review of the literature on the relationship between gut microbiota, metabolism, and MM, together with strategies to modulate the microbiota. ABSTRACT: Although novel therapies have dramatically improved outcomes for multiple myeloma (MM) patients, relapse is inevitable and overall outcomes are heterogeneous. The gut microbiota is becoming increasingly recognized for its influence on host metabolism. To date, evidence has suggested that the gut microbiota contributes to MM, not only via the progressive activities of specific bacteria but also through the influence of the microbiota on host metabolism. Importantly, the abnormal amino acid metabolism, as well as the altered microbiome in MM, is becoming increasingly apparent, as is the influence on MM progression and the therapeutic response. Moreover, the gut-microbiota–host-amino-acid metabolism interaction in the progression of MM has been highlighted. Modulation of the gut microbiota (such as fecal microbiota transplantation, FMT) can be modified, representing a new angle in MM treatment that can improve outcomes. In this review, the relationship between gut microbiota, metabolism, and MM, together with strategies to modulate the microbiota, will be discussed, and some unanswered questions for ongoing and future research will be presented. MDPI 2023-03-23 /pmc/articles/PMC10093363/ /pubmed/37046603 http://dx.doi.org/10.3390/cancers15071942 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Yang, Qin Wei, Yumou Zhu, Yinghong Guo, Jiaojiao Zhang, Jingyu He, Yanjuan Li, Xin Liu, Jing Zhou, Wen The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma |
title | The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma |
title_full | The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma |
title_fullStr | The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma |
title_full_unstemmed | The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma |
title_short | The Interaction between Gut Microbiota and Host Amino Acids Metabolism in Multiple Myeloma |
title_sort | interaction between gut microbiota and host amino acids metabolism in multiple myeloma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093363/ https://www.ncbi.nlm.nih.gov/pubmed/37046603 http://dx.doi.org/10.3390/cancers15071942 |
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