Loading…

Targeting gut microbial nitrogen recycling and cellular uptake of ammonium to improve bortezomib resistance in multiple myeloma

The gut microbiome has been found to play a crucial role in the treatment of multiple myeloma (MM), which is still considered incurable due to drug resistance. In previous studies, we demonstrated that intestinal nitrogen-recycling bacteria are enriched in patients with MM. However, their role in MM...

Full description

Saved in:
Bibliographic Details
Published in:Cell metabolism 2024-01, Vol.36 (1), p.159-175.e8
Main Authors: Zhu, Yinghong, Jian, Xingxing, Chen, Shuping, An, Gang, Jiang, Duanfeng, Yang, Qin, Zhang, Jingyu, Hu, Jian, Qiu, Yi, Feng, Xiangling, Guo, Jiaojiao, Chen, Xun, Li, Zhengjiang, Zhou, Ruiqi, Hu, Cong, He, Nihan, Shi, Fangming, Huang, Siqing, Liu, Hong, Li, Xin, Xie, Lu, Zhu, Yan, Zhao, Lia, Jiang, Yichuan, Li, Jian, Wang, Jinuo, Qiu, Lugui, Chen, Xiang, Jia, Wei, He, Yanjuan, Zhou, Wen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03
cites cdi_FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03
container_end_page 175.e8
container_issue 1
container_start_page 159
container_title Cell metabolism
container_volume 36
creator Zhu, Yinghong
Jian, Xingxing
Chen, Shuping
An, Gang
Jiang, Duanfeng
Yang, Qin
Zhang, Jingyu
Hu, Jian
Qiu, Yi
Feng, Xiangling
Guo, Jiaojiao
Chen, Xun
Li, Zhengjiang
Zhou, Ruiqi
Hu, Cong
He, Nihan
Shi, Fangming
Huang, Siqing
Liu, Hong
Li, Xin
Xie, Lu
Zhu, Yan
Zhao, Lia
Jiang, Yichuan
Li, Jian
Wang, Jinuo
Qiu, Lugui
Chen, Xiang
Jia, Wei
He, Yanjuan
Zhou, Wen
description The gut microbiome has been found to play a crucial role in the treatment of multiple myeloma (MM), which is still considered incurable due to drug resistance. In previous studies, we demonstrated that intestinal nitrogen-recycling bacteria are enriched in patients with MM. However, their role in MM relapse remains unclear. This study highlights the specific enrichment of Citrobacter freundii (C. freundii) in patients with relapsed MM. Through fecal microbial transplantation experiments, we demonstrate that C. freundii plays a critical role in inducing drug resistance in MM by increasing levels of circulating ammonium. The ammonium enters MM cells through the transmembrane channel protein SLC12A2, promoting chromosomal instability and drug resistance by stabilizing the NEK2 protein. We show that furosemide sodium, a loop diuretic, downregulates SLC12A2, thereby inhibiting ammonium uptake by MM cells and improving progression-free survival and curative effect scores. These findings provide new therapeutic targets and strategies for the intervention of MM progression and drug resistance. [Display omitted] •Citrobacter freundii can induce bortezomib resistance in patients with multiple myeloma•Ammonium can enhance NEK2 stability, inducing bortezomib resistance of myeloma cells•Furosemide administration can attenuate bortezomib resistance of myeloma cells•Probiotics like Clostridium butyricum alleviate myeloma cell resistance to bortezomib Zhu et al. demonstrated that Citrobacter freundii induces bortezomib resistance in patients with multiple myeloma by elevating circulating ammonium level. The increased ammonium enters myeloma cells, enhancing the stability of NEK2 protein. Notably, the administration of furosemide and probiotics such as Clostridium butyricum was observed to partially alleviate bortezomib resistance.
doi_str_mv 10.1016/j.cmet.2023.11.019
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2904154207</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1550413123004503</els_id><sourcerecordid>2904154207</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03</originalsourceid><addsrcrecordid>eNp9kD1PHDEQhq0oKBDgD1BELtPsMrb39kOiQShfEhIN1JbtnT35sNcX24t0NPz1eHUkZeRiXDzvq5mHkCsGNQPWXu9q4zHXHLioGauBDR_IGRsEr7qGw8fy32ygaphgp-RzSjsA0YpBfCKnomdM9H13Rt4eVdxitvOWbpdMvTUxaKscnW2OYYszjWgOxq2Amkdq0LnFqUiXfVbPSMNElfdhtounOVDr9zG8INUhZnwN3uqSTzZlNRukdqZ-cdnuHVJ_QBe8uiAnk3IJL9_nOXn6_u3x7md1__Dj193tfWUagFwx3fUDNKaMRvcjtsYMbT80vBtMC1w1nAMq3WmNyrBuGsvbTC0IgIYPI4hz8vXYW_b7vWDK0tu0HqNmDEuSvLSzTdHWFZQf0aIipYiT3EfrVTxIBnIVL3dyFS9X8ZIxWcSX0Jf3_kV7HP9F_pouwM0RwHLli8Uok7FYrIy2GM5yDPZ__X8AgZKXng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2904154207</pqid></control><display><type>article</type><title>Targeting gut microbial nitrogen recycling and cellular uptake of ammonium to improve bortezomib resistance in multiple myeloma</title><source>BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS</source><creator>Zhu, Yinghong ; Jian, Xingxing ; Chen, Shuping ; An, Gang ; Jiang, Duanfeng ; Yang, Qin ; Zhang, Jingyu ; Hu, Jian ; Qiu, Yi ; Feng, Xiangling ; Guo, Jiaojiao ; Chen, Xun ; Li, Zhengjiang ; Zhou, Ruiqi ; Hu, Cong ; He, Nihan ; Shi, Fangming ; Huang, Siqing ; Liu, Hong ; Li, Xin ; Xie, Lu ; Zhu, Yan ; Zhao, Lia ; Jiang, Yichuan ; Li, Jian ; Wang, Jinuo ; Qiu, Lugui ; Chen, Xiang ; Jia, Wei ; He, Yanjuan ; Zhou, Wen</creator><creatorcontrib>Zhu, Yinghong ; Jian, Xingxing ; Chen, Shuping ; An, Gang ; Jiang, Duanfeng ; Yang, Qin ; Zhang, Jingyu ; Hu, Jian ; Qiu, Yi ; Feng, Xiangling ; Guo, Jiaojiao ; Chen, Xun ; Li, Zhengjiang ; Zhou, Ruiqi ; Hu, Cong ; He, Nihan ; Shi, Fangming ; Huang, Siqing ; Liu, Hong ; Li, Xin ; Xie, Lu ; Zhu, Yan ; Zhao, Lia ; Jiang, Yichuan ; Li, Jian ; Wang, Jinuo ; Qiu, Lugui ; Chen, Xiang ; Jia, Wei ; He, Yanjuan ; Zhou, Wen</creatorcontrib><description>The gut microbiome has been found to play a crucial role in the treatment of multiple myeloma (MM), which is still considered incurable due to drug resistance. In previous studies, we demonstrated that intestinal nitrogen-recycling bacteria are enriched in patients with MM. However, their role in MM relapse remains unclear. This study highlights the specific enrichment of Citrobacter freundii (C. freundii) in patients with relapsed MM. Through fecal microbial transplantation experiments, we demonstrate that C. freundii plays a critical role in inducing drug resistance in MM by increasing levels of circulating ammonium. The ammonium enters MM cells through the transmembrane channel protein SLC12A2, promoting chromosomal instability and drug resistance by stabilizing the NEK2 protein. We show that furosemide sodium, a loop diuretic, downregulates SLC12A2, thereby inhibiting ammonium uptake by MM cells and improving progression-free survival and curative effect scores. These findings provide new therapeutic targets and strategies for the intervention of MM progression and drug resistance. [Display omitted] •Citrobacter freundii can induce bortezomib resistance in patients with multiple myeloma•Ammonium can enhance NEK2 stability, inducing bortezomib resistance of myeloma cells•Furosemide administration can attenuate bortezomib resistance of myeloma cells•Probiotics like Clostridium butyricum alleviate myeloma cell resistance to bortezomib Zhu et al. demonstrated that Citrobacter freundii induces bortezomib resistance in patients with multiple myeloma by elevating circulating ammonium level. The increased ammonium enters myeloma cells, enhancing the stability of NEK2 protein. Notably, the administration of furosemide and probiotics such as Clostridium butyricum was observed to partially alleviate bortezomib resistance.</description><identifier>ISSN: 1550-4131</identifier><identifier>EISSN: 1932-7420</identifier><identifier>DOI: 10.1016/j.cmet.2023.11.019</identifier><identifier>PMID: 38113887</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>ammonium ; Citrobacter freundii ; Clostridium butyricum ; furosemide ; gut microbiome ; metagenomics ; multiple myeloma ; nitrogen-recycling intestinal bacteria ; probiotics</subject><ispartof>Cell metabolism, 2024-01, Vol.36 (1), p.159-175.e8</ispartof><rights>2023 The Author(s)</rights><rights>Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03</citedby><cites>FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03</cites><orcidid>0000-0003-0834-9306 ; 0000-0002-3739-8994</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38113887$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yinghong</creatorcontrib><creatorcontrib>Jian, Xingxing</creatorcontrib><creatorcontrib>Chen, Shuping</creatorcontrib><creatorcontrib>An, Gang</creatorcontrib><creatorcontrib>Jiang, Duanfeng</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Zhang, Jingyu</creatorcontrib><creatorcontrib>Hu, Jian</creatorcontrib><creatorcontrib>Qiu, Yi</creatorcontrib><creatorcontrib>Feng, Xiangling</creatorcontrib><creatorcontrib>Guo, Jiaojiao</creatorcontrib><creatorcontrib>Chen, Xun</creatorcontrib><creatorcontrib>Li, Zhengjiang</creatorcontrib><creatorcontrib>Zhou, Ruiqi</creatorcontrib><creatorcontrib>Hu, Cong</creatorcontrib><creatorcontrib>He, Nihan</creatorcontrib><creatorcontrib>Shi, Fangming</creatorcontrib><creatorcontrib>Huang, Siqing</creatorcontrib><creatorcontrib>Liu, Hong</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Xie, Lu</creatorcontrib><creatorcontrib>Zhu, Yan</creatorcontrib><creatorcontrib>Zhao, Lia</creatorcontrib><creatorcontrib>Jiang, Yichuan</creatorcontrib><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Wang, Jinuo</creatorcontrib><creatorcontrib>Qiu, Lugui</creatorcontrib><creatorcontrib>Chen, Xiang</creatorcontrib><creatorcontrib>Jia, Wei</creatorcontrib><creatorcontrib>He, Yanjuan</creatorcontrib><creatorcontrib>Zhou, Wen</creatorcontrib><title>Targeting gut microbial nitrogen recycling and cellular uptake of ammonium to improve bortezomib resistance in multiple myeloma</title><title>Cell metabolism</title><addtitle>Cell Metab</addtitle><description>The gut microbiome has been found to play a crucial role in the treatment of multiple myeloma (MM), which is still considered incurable due to drug resistance. In previous studies, we demonstrated that intestinal nitrogen-recycling bacteria are enriched in patients with MM. However, their role in MM relapse remains unclear. This study highlights the specific enrichment of Citrobacter freundii (C. freundii) in patients with relapsed MM. Through fecal microbial transplantation experiments, we demonstrate that C. freundii plays a critical role in inducing drug resistance in MM by increasing levels of circulating ammonium. The ammonium enters MM cells through the transmembrane channel protein SLC12A2, promoting chromosomal instability and drug resistance by stabilizing the NEK2 protein. We show that furosemide sodium, a loop diuretic, downregulates SLC12A2, thereby inhibiting ammonium uptake by MM cells and improving progression-free survival and curative effect scores. These findings provide new therapeutic targets and strategies for the intervention of MM progression and drug resistance. [Display omitted] •Citrobacter freundii can induce bortezomib resistance in patients with multiple myeloma•Ammonium can enhance NEK2 stability, inducing bortezomib resistance of myeloma cells•Furosemide administration can attenuate bortezomib resistance of myeloma cells•Probiotics like Clostridium butyricum alleviate myeloma cell resistance to bortezomib Zhu et al. demonstrated that Citrobacter freundii induces bortezomib resistance in patients with multiple myeloma by elevating circulating ammonium level. The increased ammonium enters myeloma cells, enhancing the stability of NEK2 protein. Notably, the administration of furosemide and probiotics such as Clostridium butyricum was observed to partially alleviate bortezomib resistance.</description><subject>ammonium</subject><subject>Citrobacter freundii</subject><subject>Clostridium butyricum</subject><subject>furosemide</subject><subject>gut microbiome</subject><subject>metagenomics</subject><subject>multiple myeloma</subject><subject>nitrogen-recycling intestinal bacteria</subject><subject>probiotics</subject><issn>1550-4131</issn><issn>1932-7420</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kD1PHDEQhq0oKBDgD1BELtPsMrb39kOiQShfEhIN1JbtnT35sNcX24t0NPz1eHUkZeRiXDzvq5mHkCsGNQPWXu9q4zHXHLioGauBDR_IGRsEr7qGw8fy32ygaphgp-RzSjsA0YpBfCKnomdM9H13Rt4eVdxitvOWbpdMvTUxaKscnW2OYYszjWgOxq2Amkdq0LnFqUiXfVbPSMNElfdhtounOVDr9zG8INUhZnwN3uqSTzZlNRukdqZ-cdnuHVJ_QBe8uiAnk3IJL9_nOXn6_u3x7md1__Dj193tfWUagFwx3fUDNKaMRvcjtsYMbT80vBtMC1w1nAMq3WmNyrBuGsvbTC0IgIYPI4hz8vXYW_b7vWDK0tu0HqNmDEuSvLSzTdHWFZQf0aIipYiT3EfrVTxIBnIVL3dyFS9X8ZIxWcSX0Jf3_kV7HP9F_pouwM0RwHLli8Uok7FYrIy2GM5yDPZ__X8AgZKXng</recordid><startdate>20240102</startdate><enddate>20240102</enddate><creator>Zhu, Yinghong</creator><creator>Jian, Xingxing</creator><creator>Chen, Shuping</creator><creator>An, Gang</creator><creator>Jiang, Duanfeng</creator><creator>Yang, Qin</creator><creator>Zhang, Jingyu</creator><creator>Hu, Jian</creator><creator>Qiu, Yi</creator><creator>Feng, Xiangling</creator><creator>Guo, Jiaojiao</creator><creator>Chen, Xun</creator><creator>Li, Zhengjiang</creator><creator>Zhou, Ruiqi</creator><creator>Hu, Cong</creator><creator>He, Nihan</creator><creator>Shi, Fangming</creator><creator>Huang, Siqing</creator><creator>Liu, Hong</creator><creator>Li, Xin</creator><creator>Xie, Lu</creator><creator>Zhu, Yan</creator><creator>Zhao, Lia</creator><creator>Jiang, Yichuan</creator><creator>Li, Jian</creator><creator>Wang, Jinuo</creator><creator>Qiu, Lugui</creator><creator>Chen, Xiang</creator><creator>Jia, Wei</creator><creator>He, Yanjuan</creator><creator>Zhou, Wen</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0834-9306</orcidid><orcidid>https://orcid.org/0000-0002-3739-8994</orcidid></search><sort><creationdate>20240102</creationdate><title>Targeting gut microbial nitrogen recycling and cellular uptake of ammonium to improve bortezomib resistance in multiple myeloma</title><author>Zhu, Yinghong ; Jian, Xingxing ; Chen, Shuping ; An, Gang ; Jiang, Duanfeng ; Yang, Qin ; Zhang, Jingyu ; Hu, Jian ; Qiu, Yi ; Feng, Xiangling ; Guo, Jiaojiao ; Chen, Xun ; Li, Zhengjiang ; Zhou, Ruiqi ; Hu, Cong ; He, Nihan ; Shi, Fangming ; Huang, Siqing ; Liu, Hong ; Li, Xin ; Xie, Lu ; Zhu, Yan ; Zhao, Lia ; Jiang, Yichuan ; Li, Jian ; Wang, Jinuo ; Qiu, Lugui ; Chen, Xiang ; Jia, Wei ; He, Yanjuan ; Zhou, Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>ammonium</topic><topic>Citrobacter freundii</topic><topic>Clostridium butyricum</topic><topic>furosemide</topic><topic>gut microbiome</topic><topic>metagenomics</topic><topic>multiple myeloma</topic><topic>nitrogen-recycling intestinal bacteria</topic><topic>probiotics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yinghong</creatorcontrib><creatorcontrib>Jian, Xingxing</creatorcontrib><creatorcontrib>Chen, Shuping</creatorcontrib><creatorcontrib>An, Gang</creatorcontrib><creatorcontrib>Jiang, Duanfeng</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Zhang, Jingyu</creatorcontrib><creatorcontrib>Hu, Jian</creatorcontrib><creatorcontrib>Qiu, Yi</creatorcontrib><creatorcontrib>Feng, Xiangling</creatorcontrib><creatorcontrib>Guo, Jiaojiao</creatorcontrib><creatorcontrib>Chen, Xun</creatorcontrib><creatorcontrib>Li, Zhengjiang</creatorcontrib><creatorcontrib>Zhou, Ruiqi</creatorcontrib><creatorcontrib>Hu, Cong</creatorcontrib><creatorcontrib>He, Nihan</creatorcontrib><creatorcontrib>Shi, Fangming</creatorcontrib><creatorcontrib>Huang, Siqing</creatorcontrib><creatorcontrib>Liu, Hong</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Xie, Lu</creatorcontrib><creatorcontrib>Zhu, Yan</creatorcontrib><creatorcontrib>Zhao, Lia</creatorcontrib><creatorcontrib>Jiang, Yichuan</creatorcontrib><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Wang, Jinuo</creatorcontrib><creatorcontrib>Qiu, Lugui</creatorcontrib><creatorcontrib>Chen, Xiang</creatorcontrib><creatorcontrib>Jia, Wei</creatorcontrib><creatorcontrib>He, Yanjuan</creatorcontrib><creatorcontrib>Zhou, Wen</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cell metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Yinghong</au><au>Jian, Xingxing</au><au>Chen, Shuping</au><au>An, Gang</au><au>Jiang, Duanfeng</au><au>Yang, Qin</au><au>Zhang, Jingyu</au><au>Hu, Jian</au><au>Qiu, Yi</au><au>Feng, Xiangling</au><au>Guo, Jiaojiao</au><au>Chen, Xun</au><au>Li, Zhengjiang</au><au>Zhou, Ruiqi</au><au>Hu, Cong</au><au>He, Nihan</au><au>Shi, Fangming</au><au>Huang, Siqing</au><au>Liu, Hong</au><au>Li, Xin</au><au>Xie, Lu</au><au>Zhu, Yan</au><au>Zhao, Lia</au><au>Jiang, Yichuan</au><au>Li, Jian</au><au>Wang, Jinuo</au><au>Qiu, Lugui</au><au>Chen, Xiang</au><au>Jia, Wei</au><au>He, Yanjuan</au><au>Zhou, Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting gut microbial nitrogen recycling and cellular uptake of ammonium to improve bortezomib resistance in multiple myeloma</atitle><jtitle>Cell metabolism</jtitle><addtitle>Cell Metab</addtitle><date>2024-01-02</date><risdate>2024</risdate><volume>36</volume><issue>1</issue><spage>159</spage><epage>175.e8</epage><pages>159-175.e8</pages><issn>1550-4131</issn><eissn>1932-7420</eissn><abstract>The gut microbiome has been found to play a crucial role in the treatment of multiple myeloma (MM), which is still considered incurable due to drug resistance. In previous studies, we demonstrated that intestinal nitrogen-recycling bacteria are enriched in patients with MM. However, their role in MM relapse remains unclear. This study highlights the specific enrichment of Citrobacter freundii (C. freundii) in patients with relapsed MM. Through fecal microbial transplantation experiments, we demonstrate that C. freundii plays a critical role in inducing drug resistance in MM by increasing levels of circulating ammonium. The ammonium enters MM cells through the transmembrane channel protein SLC12A2, promoting chromosomal instability and drug resistance by stabilizing the NEK2 protein. We show that furosemide sodium, a loop diuretic, downregulates SLC12A2, thereby inhibiting ammonium uptake by MM cells and improving progression-free survival and curative effect scores. These findings provide new therapeutic targets and strategies for the intervention of MM progression and drug resistance. [Display omitted] •Citrobacter freundii can induce bortezomib resistance in patients with multiple myeloma•Ammonium can enhance NEK2 stability, inducing bortezomib resistance of myeloma cells•Furosemide administration can attenuate bortezomib resistance of myeloma cells•Probiotics like Clostridium butyricum alleviate myeloma cell resistance to bortezomib Zhu et al. demonstrated that Citrobacter freundii induces bortezomib resistance in patients with multiple myeloma by elevating circulating ammonium level. The increased ammonium enters myeloma cells, enhancing the stability of NEK2 protein. Notably, the administration of furosemide and probiotics such as Clostridium butyricum was observed to partially alleviate bortezomib resistance.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38113887</pmid><doi>10.1016/j.cmet.2023.11.019</doi><orcidid>https://orcid.org/0000-0003-0834-9306</orcidid><orcidid>https://orcid.org/0000-0002-3739-8994</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1550-4131
ispartof Cell metabolism, 2024-01, Vol.36 (1), p.159-175.e8
issn 1550-4131
1932-7420
language eng
recordid cdi_proquest_miscellaneous_2904154207
source BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS
subjects ammonium
Citrobacter freundii
Clostridium butyricum
furosemide
gut microbiome
metagenomics
multiple myeloma
nitrogen-recycling intestinal bacteria
probiotics
title Targeting gut microbial nitrogen recycling and cellular uptake of ammonium to improve bortezomib resistance in multiple myeloma
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T16%3A07%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Targeting%20gut%20microbial%20nitrogen%20recycling%20and%20cellular%20uptake%20of%20ammonium%20to%20improve%20bortezomib%20resistance%20in%20multiple%20myeloma&rft.jtitle=Cell%20metabolism&rft.au=Zhu,%20Yinghong&rft.date=2024-01-02&rft.volume=36&rft.issue=1&rft.spage=159&rft.epage=175.e8&rft.pages=159-175.e8&rft.issn=1550-4131&rft.eissn=1932-7420&rft_id=info:doi/10.1016/j.cmet.2023.11.019&rft_dat=%3Cproquest_cross%3E2904154207%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c400t-1b78904cb784b8de6cc96894279c602a4220eab7bbeac17fdfdf5f60300429d03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2904154207&rft_id=info:pmid/38113887&rfr_iscdi=true