基于核磁共振的尿液代谢谱如何早期检测胰腺肿瘤?胰腺癌原位异种移植小鼠模型中肿瘤发生和发展的早期生物标志物的鉴定。

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Metabolites Pub Date : 2025-02-20 DOI:10.3390/metabo15030142
Tafadzwa Chihanga, Shenyuan Xu, Hannah N Fultz, Jenna D Nicholson, Mark D Brombacher, Kayla Hawkins, Dan R Fay, Maria M Steil, Shuisong Ni, Michael A Kennedy
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引用次数: 0

摘要

背景:胰腺癌是所有人类癌症中最致命的。这种疾病在早期阶段没有明显的症状,在大多数情况下,直到癌症发展到手术不再可行的地步,或者直到它已经转移到其他器官,才会被发现。缺乏可靠和敏感的早期检测胰腺癌的生物标志物,导致在疾病发展到无法治疗的阶段之前检测疾病的能力较差。目的:在此,我们研究了一种原位异种移植胰腺癌小鼠模型,以确定尿代谢生物标志物是否可以识别并用于检测胰腺肿瘤的早期形成。方法:将来自65岁男性胰腺腺癌患者的人MiaPaCa-2细胞注入重度联合免疫缺陷小鼠胰腺,建立胰腺癌原位异种移植小鼠模型。原位胰腺肿瘤生长8周后,成功地在20只小鼠中的15只小鼠的胰腺中建立。在牺牲时,切除肿瘤,进行组织学分析,并记录肿块和体积。在注射前、注射后一周和注射后每两周采集一次尿样,共8周。结果:基于核磁共振的尿液样本代谢谱显示,在肿瘤发生和生长过程中,31种代谢物发生了显著变化。纵向代谢分析表明,参与癌细胞能量产生和/或细胞合成的代谢途径的活性最初增加,这是支持肿瘤生长所必需的,随后,当肿瘤达到注射后7-8周时,对照和原位小鼠之间与肿瘤衰老相关的差异减小。结论:研究结果表明,基于核磁共振的尿代谢谱分析可能能够检测胰腺肿瘤发生和生长的早期阶段,突出了转化为人类临床研究的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How Early Can Pancreatic Tumors Be Detected Using NMR-Based Urine Metabolic Profiling? Identification of Early-Stage Biomarkers of Tumor Initiation and Progression in an Orthotopic Xenograft Mouse Model of Pancreatic Cancer.

Background: Pancreatic cancer is the most lethal of all human cancers. The disease has no obvious symptoms in its early stages and in the majority of cases, the cancer goes undetected until it has advanced to the point that surgery is no longer a viable option or until it has metastasized to other organs. The absence of reliable and sensitive biomarkers for the early detection of pancreatic cancer contributes to the poor ability to detect the disease before it progresses to an untreatable stage. Objectives: Here, an orthotopic xenograft mouse model of pancreatic cancer was investigated to determine if urinary metabolic biomarkers could be identified and used to detect the early formation of pancreatic tumors. Methods: The orthotopic xenograft mouse model of pancreatic cancer was established by injecting human MiaPaCa-2 cells, derived from a male patient aged 65 years with pancreatic adenocarcinoma, into the pancreata of severe combined immunodeficient mice. Orthotopic pancreatic tumors, allowed to grow for eight weeks, were successfully established in the pancreata in 15 out of 20 mice. At the time of sacrifice, tumors were excised and histologically analyzed and the masses and volumes recorded. Urine samples were collected prior to injection, at one-week post injection, and every two weeks afterwards for eight weeks. Results: NMR-based metabolic profiling of the urine samples indicated that 31 metabolites changed significantly over the course of tumor initiation and growth. Longitudinal metabolic profiling analysis indicated an initial increase in activity of the metabolic pathways involved in energy production and/or cell synthesis by cancer cells as required to support tumor growth that was followed by a diminished difference between control and orthotopic mice associated with tumor senescence as the tumors reached 7-8 weeks post injection. Conclusions: The results indicate that NMR-based urinary metabolic profiling may be able to detect the earliest stages of pancreatic tumor initiation and growth, highlighting the potential for translation to human clinical studies.

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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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