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代谢组学分析揭示唾液中亚牛磺酸可能成为药物相关性颌骨坏死的早期检测标志物。

Metabolomic profiling reveals salivary hypotaurine as a potential early detection marker for medication-related osteonecrosis of the jaw.

机构信息

Dental Division, National Cancer Center Hospital, Tsukiji, Chuo-ku, Japan.

Course of Advanced Clinical Research of Cancer, Juntendo University Graduate School of Medicine, Hongo, Bunkyo-ku, Tokyo, Japan.

出版信息

PLoS One. 2019 Aug 12;14(8):e0220712. doi: 10.1371/journal.pone.0220712. eCollection 2019.

DOI:10.1371/journal.pone.0220712
PMID:31404085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6690531/
Abstract

Medication-related osteonecrosis of the jaw (MRONJ) is a rare but serious adverse event of bone-modifying agents used to prevent bone complications in cancer patients with bone metastasis. Currently, early treatment is the only way to prevent further progression, as the pathogenesis of MRONJ has not yet been elucidated, and a standard treatment has not been established. The aim of this study was to identify a marker for early detection marker of MRONJ by exploring substances in saliva specific to MRONJ at an early stage. We collected salivary samples from 17 patients with MRONJ and conducted metabolomic analyses using capillary electrophoresis mass spectrometry for non-targeted analysis of hydrophilic metabolites. In the screening cohort, we compared the saliva of patients with stage ≥1 advanced MRONJ (n = 9) with that of controls without MRONJ before chemotherapy (n = 9). The top 5 most elevated salivary metabolites were histamine, 3-(4-hydroxyphenyl)propionate, malonate, carnosine, and hypotaurine. In the validation cohort, we analyzed additional patients with stage ≥1 advanced MRONJ (n = 8) and controls without MRONJ after chemotherapy (n = 9), confirming a significant 2.28-fold elevation in the salivary concentration of hypotaurine. These results revealed elevated salivary hypotaurine concentration as a potential marker for the early detection of MRONJ.

摘要

药物相关性下颌骨坏死(MRONJ)是一种罕见但严重的骨骼修饰剂的不良反应,用于预防有骨转移的癌症患者的骨骼并发症。目前,早期治疗是防止进一步进展的唯一方法,因为 MRONJ 的发病机制尚未阐明,也没有确立标准的治疗方法。本研究旨在通过探索早期 MRONJ 特异性唾液物质,寻找用于早期检测的标志物。我们收集了 17 例 MRONJ 患者的唾液样本,并使用毛细管电泳质谱进行非靶向亲水代谢物分析。在筛选队列中,我们比较了 9 例化疗前无 MRONJ 的对照组和 9 例≥1 期晚期 MRONJ 患者的唾液。在前 5 个升高的唾液代谢物中,组胺、3-(4-羟苯基)丙酸、丙二酸、肌肽和牛磺酸的含量较高。在验证队列中,我们分析了另外 8 例≥1 期晚期 MRONJ 患者和 9 例化疗后无 MRONJ 的对照组,验证了牛磺酸的唾液浓度显著升高了 2.28 倍。这些结果揭示了升高的唾液牛磺酸浓度作为 MRONJ 早期检测的潜在标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/f5e4b47bf9b9/pone.0220712.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/be59834fcde2/pone.0220712.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/b4985c1a327f/pone.0220712.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/eff21e620a2c/pone.0220712.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/9e4ec6ade85f/pone.0220712.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/f5e4b47bf9b9/pone.0220712.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/be59834fcde2/pone.0220712.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/b4985c1a327f/pone.0220712.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/eff21e620a2c/pone.0220712.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/9e4ec6ade85f/pone.0220712.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2107/6690531/f5e4b47bf9b9/pone.0220712.g005.jpg

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本文引用的文献

1
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Clin Chim Acta. 2019 Feb;489:41-48. doi: 10.1016/j.cca.2018.11.030. Epub 2018 Nov 24.
2
Effect of storage conditions on salivary polyamines quantified via liquid chromatography-mass spectrometry.基于液质联用技术检测唾液多胺的储存条件影响。
Sci Rep. 2018 Aug 13;8(1):12075. doi: 10.1038/s41598-018-30482-x.
3
Severe Maxillary Medication-related Osteonecrosis of the Jaw.严重的上颌骨药物相关性颌骨坏死
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Front Med (Lausanne). 2023 Aug 31;10:1164051. doi: 10.3389/fmed.2023.1164051. eCollection 2023.
4
Salivary Metabolomics for Oral Cancer Detection: A Narrative Review.用于口腔癌检测的唾液代谢组学:一篇综述。
Metabolites. 2022 May 12;12(5):436. doi: 10.3390/metabo12050436.
5
Salivary Metabolomics for Diagnosis and Monitoring Diseases: Challenges and Possibilities.用于疾病诊断和监测的唾液代谢组学:挑战与机遇
Metabolites. 2021 Aug 31;11(9):587. doi: 10.3390/metabo11090587.
6
Time-Course of Salivary Metabolomic Profiles during Radiation Therapy for Head and Neck Cancer.头颈癌放射治疗期间唾液代谢组学图谱的时间进程
J Clin Med. 2021 Jun 15;10(12):2631. doi: 10.3390/jcm10122631.
7
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Antioxidants (Basel). 2021 Apr 27;10(5):680. doi: 10.3390/antiox10050680.
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9
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4
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6
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10
Comments on "diagnosis and management of osteonecrosis of the jaw: a systematic review and international consensus".关于《颌骨骨坏死的诊断与管理:系统评价与国际共识》的评论
J Bone Miner Res. 2015 Jun;30(6):1113-5. doi: 10.1002/jbmr.2525.