Circulating adipose-tissue miRNAs in gastrointestinal cancer patients and their association with the level and type of adiposity at body composition analysis

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Federica Tambaro, Giovanni Imbimbo, Valentina Pace, Maria Ida Amabile, Veronica Rizzo, Simona Orlando, Giulia Lauteri, Cesarina Ramaccini, Carlo Catalano, Giuseppe Nigri, Maurizio Muscaritoli, Alessio Molfino
{"title":"Circulating adipose-tissue miRNAs in gastrointestinal cancer patients and their association with the level and type of adiposity at body composition analysis","authors":"Federica Tambaro, Giovanni Imbimbo, Valentina Pace, Maria Ida Amabile, Veronica Rizzo, Simona Orlando, Giulia Lauteri, Cesarina Ramaccini, Carlo Catalano, Giuseppe Nigri, Maurizio Muscaritoli, Alessio Molfino","doi":"10.3389/fmolb.2024.1449197","DOIUrl":null,"url":null,"abstract":"BackgroundAdipose tissue (AT) wasting in cancer is an early catabolic event with negative impact on outcomes. Circulating miRNAs may promote body weight loss and cachexia. We measured circulating miRNAs linked to AT alterations and compared their levels between i) gastrointestinal (GI) cancer patients and controls, ii) cachectic and non-cachectic cancer patients, and iii) according to adiposity level and its distribution.MethodsPatients with GI cancer and subjects with benign diseases as controls were considered. Cachexia was assessed and adiposity evaluated by CT-scan for subcutaneous AT area (SAT), visceral AT area and the total AT area (TAT). MiRNAs involved were measured in plasma by RT-qPCR.Results37 naïve GI cancer patients and 14 controls were enrolled. Patients with cachexia presented with lower SAT compared to non-cachectic (<jats:italic>p</jats:italic> &amp;lt; 0.05). In cancer patients, we found higher levels of miR-26a, miR-128, miR-155 and miR-181a vs. controls (<jats:italic>p</jats:italic> &amp;lt; 0.05). Cancer patients with BMI <jats:inline-formula><mml:math xmlns:mml=\"http://www.w3.org/1998/Math/MathML\"><mml:mrow><mml:mo>&lt;</mml:mo></mml:mrow></mml:math></jats:inline-formula> 25 kg/m<jats:sup>2</jats:sup> showed higher levels of miR-26a vs. those with BMI <jats:inline-formula><mml:math xmlns:mml=\"http://www.w3.org/1998/Math/MathML\"><mml:mrow><mml:mo>≥</mml:mo></mml:mrow></mml:math></jats:inline-formula> 25 (<jats:italic>p</jats:italic> = 0.035). MiR-26a and miR-181a were higher in cachectic and non-cachectic vs. controls (<jats:italic>p</jats:italic> &amp;lt; 0.05). Differences between cachectic and controls were confirmed for miR-155 (<jats:italic>p</jats:italic> &amp;lt; 0.001) but not between non-cachectic vs. control (<jats:italic>p</jats:italic> = 0.072). MiR-155 was higher in cachectic patients with low TAT vs. those without cachexia and high TAT (<jats:italic>p</jats:italic> = 0.036).ConclusionOur data confirm a modulation of specific and different miRNAs involved in AT metabolism in cancer and cachexia. MiR-155 levels were higher in patients presenting with cachexia and low adiposity with implications in the pathogenic mechanisms and clinical consequences of GI cancer patients.","PeriodicalId":12465,"journal":{"name":"Frontiers in Molecular Biosciences","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Molecular Biosciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmolb.2024.1449197","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

BackgroundAdipose tissue (AT) wasting in cancer is an early catabolic event with negative impact on outcomes. Circulating miRNAs may promote body weight loss and cachexia. We measured circulating miRNAs linked to AT alterations and compared their levels between i) gastrointestinal (GI) cancer patients and controls, ii) cachectic and non-cachectic cancer patients, and iii) according to adiposity level and its distribution.MethodsPatients with GI cancer and subjects with benign diseases as controls were considered. Cachexia was assessed and adiposity evaluated by CT-scan for subcutaneous AT area (SAT), visceral AT area and the total AT area (TAT). MiRNAs involved were measured in plasma by RT-qPCR.Results37 naïve GI cancer patients and 14 controls were enrolled. Patients with cachexia presented with lower SAT compared to non-cachectic (p &lt; 0.05). In cancer patients, we found higher levels of miR-26a, miR-128, miR-155 and miR-181a vs. controls (p &lt; 0.05). Cancer patients with BMI < 25 kg/m2 showed higher levels of miR-26a vs. those with BMI 25 (p = 0.035). MiR-26a and miR-181a were higher in cachectic and non-cachectic vs. controls (p &lt; 0.05). Differences between cachectic and controls were confirmed for miR-155 (p &lt; 0.001) but not between non-cachectic vs. control (p = 0.072). MiR-155 was higher in cachectic patients with low TAT vs. those without cachexia and high TAT (p = 0.036).ConclusionOur data confirm a modulation of specific and different miRNAs involved in AT metabolism in cancer and cachexia. MiR-155 levels were higher in patients presenting with cachexia and low adiposity with implications in the pathogenic mechanisms and clinical consequences of GI cancer patients.
胃肠道癌症患者的循环脂肪组织 miRNA 及其与身体成分分析中脂肪水平和类型的关系
背景癌症患者的脂肪组织(AT)消瘦是一种早期分解代谢现象,会对预后产生负面影响。循环 miRNA 可促进体重减轻和恶病质。我们测定了与胃肠道组织变化有关的循环 miRNAs,并比较了胃肠道(GI)癌症患者和对照组、②恶病质和非恶病质癌症患者以及③根据脂肪水平及其分布情况测定的 miRNAs 的水平。通过 CT 扫描对皮下 AT 面积(SAT)、内脏 AT 面积和总 AT 面积(TAT)进行评估。通过 RT-qPCR 测量了血浆中相关的 MiRNA。与非恶病质患者相比,恶病质患者的 SAT 较低(pamp &;lt;0.05)。在癌症患者中,我们发现 miR-26a、miR-128、miR-155 和 miR-181a 的水平高于对照组(p &;lt; 0.05)。与体重指数≥25的癌症患者相比,体重指数≥25的癌症患者的miR-26a水平更高(p = 0.035)。与对照组相比,恶性肿瘤患者和非恶性肿瘤患者的 MiR-26a 和 miR-181a 水平更高(p &;lt;0.05)。miR-155证实了恶性肿瘤患者与对照组之间的差异(p &;lt;0.001),但非恶性肿瘤患者与对照组之间的差异没有得到证实(p = 0.072)。结论我们的数据证实了癌症和恶病质中参与 AT 代谢的特定和不同的 miRNA 受调控。MiR-155水平在出现恶病质和低脂肪的患者中较高,这对消化道癌症患者的致病机制和临床后果有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信