• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

FTO——肥胖与癌症的共同遗传基础。

FTO - A Common Genetic Basis for Obesity and Cancer.

作者信息

Lan Ning, Lu Ying, Zhang Yigan, Pu Shuangshuang, Xi Huaze, Nie Xin, Liu Jing, Yuan Wenzhen

机构信息

The First School of Clinical Medicine, Lanzhou University, Lanzhou, China.

The First Hospital of Lanzhou University, Lanzhou, China.

出版信息

Front Genet. 2020 Nov 16;11:559138. doi: 10.3389/fgene.2020.559138. eCollection 2020.

DOI:10.3389/fgene.2020.559138
PMID:33304380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7701174/
Abstract

In recent years, the prevalence of obesity and cancer have been rising. Since this poses a serious threat to human health, the relationship between the two has attracted much attention. This study examined whether fat mass and obesity-associated () genes are linked, taking into account a Genome-wide Association Study (GWAS) that revealed multiple single nucleotide polymorphism sites (SNPs) of the gene, indicating an association between obesity and cancer in different populations. FTO proteins have been proved to participate in adipogenesis and tumorigenesis with post-transcriptional regulation of downstream molecular expression or through the target of the mammalian target protein rapamycin (mTOR). FTO inhibitors have also been found to share anti-obesity and anti-cancer effects . In this review, we comprehensively discuss the correlation between obesity and cancer by measuring gene polymorphism, as well as the molecular mechanism involved in these diseases, emphasizing FTO as the common genetic basis of obesity and cancer.

摘要

近年来,肥胖症和癌症的患病率一直在上升。由于这对人类健康构成严重威胁,两者之间的关系备受关注。本研究考虑到一项全基因组关联研究(GWAS)揭示了该基因的多个单核苷酸多态性位点(SNP),表明肥胖与不同人群的癌症之间存在关联,从而检验了脂肪量与肥胖相关()基因是否有关联。FTO蛋白已被证明通过对下游分子表达的转录后调控或通过哺乳动物雷帕霉素靶蛋白(mTOR)靶点参与脂肪生成和肿瘤发生。还发现FTO抑制剂具有抗肥胖和抗癌作用。在本综述中,我们通过测量基因多态性全面讨论肥胖与癌症之间的相关性,以及这些疾病所涉及的分子机制,强调FTO作为肥胖和癌症的共同遗传基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/ec6f18f43790/fgene-11-559138-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/e2f8d8a51901/fgene-11-559138-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/0d6fec6dd69f/fgene-11-559138-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/ec6f18f43790/fgene-11-559138-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/e2f8d8a51901/fgene-11-559138-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/0d6fec6dd69f/fgene-11-559138-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be27/7701174/ec6f18f43790/fgene-11-559138-g003.jpg

相似文献

1
FTO - A Common Genetic Basis for Obesity and Cancer.FTO——肥胖与癌症的共同遗传基础。
Front Genet. 2020 Nov 16;11:559138. doi: 10.3389/fgene.2020.559138. eCollection 2020.
2
Critical Enzymatic Functions of FTO in Obesity and Cancer.肥胖与癌症中FTO的关键酶功能
Front Endocrinol (Lausanne). 2018 Jul 30;9:396. doi: 10.3389/fendo.2018.00396. eCollection 2018.
3
Complex Relationship between Obesity and the Fat Mass and Obesity Locus.肥胖与脂肪量和肥胖基因座之间的复杂关系
Int J Biol Sci. 2017 May 15;13(5):615-629. doi: 10.7150/ijbs.17051. eCollection 2017.
4
The role of the FTO (Fat Mass and Obesity Related) locus in regulating body size and composition.FTO(肥胖相关)基因座在调节身体大小和组成方面的作用。
Mol Cell Endocrinol. 2014 Nov;397(1-2):34-41. doi: 10.1016/j.mce.2014.09.012. Epub 2014 Sep 16.
5
The 'Fat Mass and Obesity Related' (FTO) gene: Mechanisms of Impact on Obesity and Energy Balance.“脂肪量与肥胖相关”(FTO)基因:对肥胖和能量平衡的影响机制
Curr Obes Rep. 2015 Mar;4(1):73-91. doi: 10.1007/s13679-015-0143-1.
6
Roles of N6-Methyladenosine Demethylase FTO in Malignant Tumors Progression.N6-甲基腺苷去甲基化酶FTO在恶性肿瘤进展中的作用
Onco Targets Ther. 2021 Sep 16;14:4837-4846. doi: 10.2147/OTT.S329232. eCollection 2021.
7
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.早发性极度肥胖的全基因组关联(GWA)研究支持脂肪量和肥胖相关基因(FTO)变异的作用。
PLoS One. 2007 Dec 26;2(12):e1361. doi: 10.1371/journal.pone.0001361.
8
Studies on the fat mass and obesity-associated (FTO) gene and its impact on obesity-associated diseases.脂肪量和肥胖相关(FTO)基因及其对肥胖相关疾病影响的研究。
Genes Dis. 2022 May 6;10(6):2351-2365. doi: 10.1016/j.gendis.2022.04.014. eCollection 2023 Nov.
9
The Potential Role of N6-Methyladenosine (m6A) Demethylase Fat Mass and Obesity-Associated Gene (FTO) in Human Cancers.N6-甲基腺苷(m6A)去甲基化酶脂肪量与肥胖相关基因(FTO)在人类癌症中的潜在作用
Onco Targets Ther. 2020 Dec 15;13:12845-12856. doi: 10.2147/OTT.S283417. eCollection 2020.
10
FTO Gene Affects Obesity and Breast Cancer Through Similar Mechanisms: A New Insight into the Molecular Therapeutic Targets.FTO基因通过相似机制影响肥胖和乳腺癌:对分子治疗靶点的新见解
Nutr Cancer. 2018 Jan;70(1):30-36. doi: 10.1080/01635581.2018.1397709. Epub 2017 Dec 8.

引用本文的文献

1
The Role of Fat Mass and Obesity-Associated (FTO) Gene in Non-Small Cell Lung Cancer Tumorigenicity and EGFR Tyrosine Kinase Inhibitor Resistance.脂肪量与肥胖相关(FTO)基因在非小细胞肺癌致瘤性及表皮生长因子受体酪氨酸激酶抑制剂耐药性中的作用
Biomedicines. 2025 Jul 7;13(7):1653. doi: 10.3390/biomedicines13071653.
2
FTO O-GlcNAcylation promotes TRIM21-mediated FTO ubiquitination degradation to sustain the negative feedback control of macrophage inflammation.FTO的O-连接N-乙酰葡糖胺化促进TRIM21介导的FTO泛素化降解,以维持巨噬细胞炎症的负反馈控制。
Front Immunol. 2025 Jun 26;16:1593243. doi: 10.3389/fimmu.2025.1593243. eCollection 2025.
3

本文引用的文献

1
The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults.FTO rs9939609 基因多态性与成年人人体测量指数的关联。
J Physiol Anthropol. 2020 May 12;39(1):14. doi: 10.1186/s40101-020-00224-y.
2
Rs9939609 polymorphism of the fat mass and obesity-associated (FTO) gene and metabolic syndrome susceptibility in the Chinese population: a meta-analysis.中国人群中脂肪量和肥胖相关(FTO)基因的Rs9939609多态性与代谢综合征易感性的Meta分析
Endocrine. 2020 Aug;69(2):278-285. doi: 10.1007/s12020-020-02280-x. Epub 2020 Apr 17.
3
FTO rs9939609 influence on adipose tissue localization in the Italian population.
Anthropometrics, cancer risks, and survival outcomes in adult patients with glioma - a systematic review and meta-analysis.
成人胶质瘤患者的人体测量学、癌症风险和生存结局——一项系统评价和荟萃分析
Acta Neurochir (Wien). 2025 Jul 10;167(1):188. doi: 10.1007/s00701-025-06579-4.
4
Characterizing Genetic, Epigenetic, Nutritional, and Clinico-Biochemical Profile of Women With Polycystic Ovary Syndrome: A Case-Control Study.多囊卵巢综合征女性的遗传、表观遗传、营养及临床生化特征:一项病例对照研究
J Nutr Metab. 2025 May 30;2025:8817919. doi: 10.1155/jnme/8817919. eCollection 2025.
5
Insights into the molecular and genetic role of obesity in breast cancer pathogenesis.肥胖在乳腺癌发病机制中的分子和遗传作用的见解。
Cancer Biol Ther. 2025 Dec;26(1):2501345. doi: 10.1080/15384047.2025.2501345. Epub 2025 May 12.
6
FTO-mediated m6A demethylation of KLF4 promotes the proliferation and collagen deposition of keloid fibroblasts.FTO介导的KLF4的m6A去甲基化促进瘢痕疙瘩成纤维细胞的增殖和胶原沉积。
Toxicol Res (Camb). 2025 Apr 26;14(2):tfaf058. doi: 10.1093/toxres/tfaf058. eCollection 2025 Apr.
7
Genetic Insights into Breast Cancer in Northeastern Mexico: Unveiling Gene-Environment Interactions and Their Links to Obesity and Metabolic Diseases.墨西哥东北部乳腺癌的遗传学见解:揭示基因-环境相互作用及其与肥胖和代谢性疾病的联系。
Cancers (Basel). 2025 Mar 14;17(6):982. doi: 10.3390/cancers17060982.
8
Protective Effect of Semaglutide on Obesity-Induced Renal Disease and Obesity-Induced Kidney Renal Clear Cell Carcinoma.司美格鲁肽对肥胖诱导的肾脏疾病及肥胖诱导的肾透明细胞癌的保护作用
Diabetes Metab Syndr Obes. 2025 Mar 19;18:805-818. doi: 10.2147/DMSO.S498447. eCollection 2025.
9
Therapeutic Potential of FTO Demethylase in Metabolism and Disease Pathways.FTO去甲基化酶在代谢和疾病途径中的治疗潜力
Protein J. 2025 Feb;44(1):21-34. doi: 10.1007/s10930-025-10250-3. Epub 2025 Feb 9.
10
rs17817449 Variant Increases the Risk of Severe Obesity in a Brazilian Cohort: A Case-Control Study.rs17817449变异体增加巴西队列中严重肥胖风险:一项病例对照研究
Diabetes Metab Syndr Obes. 2025 Jan 31;18:283-303. doi: 10.2147/DMSO.S451401. eCollection 2025.
FTO rs9939609 对意大利人群脂肪组织定位的影响。
Eur Rev Med Pharmacol Sci. 2020 Mar;24(6):3223-3235. doi: 10.26355/eurrev_202003_20689.
4
Transcription factorIRX5 promotes hepatocellular carcinoma proliferation and inhibits apoptosis by regulating the p53 signalling pathway.转录因子IRX5通过调控p53信号通路促进肝细胞癌增殖并抑制凋亡。
Cell Biochem Funct. 2020 Jul;38(5):621-629. doi: 10.1002/cbf.3517. Epub 2020 Mar 9.
5
Association of rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults.rs9939609 多态性与超重成年人血清瘦素、胰岛素、脂联素和血脂谱的关联。
Adipocyte. 2020 Dec;9(1):51-56. doi: 10.1080/21623945.2020.1722550.
6
Synergistic inhibition of lung cancer cells by EGCG and NF-κB inhibitor BAY11-7082.表没食子儿茶素没食子酸酯(EGCG)与核因子κB(NF-κB)抑制剂BAY11-7082对肺癌细胞的协同抑制作用
J Cancer. 2019 Oct 21;10(26):6543-6556. doi: 10.7150/jca.34285. eCollection 2019.
7
m6A demethylase FTO promotes hepatocellular carcinoma tumorigenesis via mediating PKM2 demethylation.m6A去甲基化酶FTO通过介导丙酮酸激酶M2(PKM2)去甲基化促进肝细胞癌的肿瘤发生。
Am J Transl Res. 2019 Sep 15;11(9):6084-6092. eCollection 2019.
8
The weight of obesity in breast cancer progression and metastasis: Clinical and molecular perspectives.肥胖在乳腺癌进展和转移中的作用:临床和分子观点。
Semin Cancer Biol. 2020 Feb;60:274-284. doi: 10.1016/j.semcancer.2019.09.001. Epub 2019 Sep 3.
9
IRX5 promotes colorectal cancer metastasis by negatively regulating the core components of the RHOA pathway.IRX5 通过负向调控 RHOA 通路的核心组件促进结直肠癌转移。
Mol Carcinog. 2019 Nov;58(11):2065-2076. doi: 10.1002/mc.23098. Epub 2019 Aug 20.
10
Epigallocatechin-3-Gallate (EGCG) Suppresses Pancreatic Cancer Cell Growth, Invasion, and Migration partly through the Inhibition of Akt Pathway and Epithelial-Mesenchymal Transition: Enhanced Efficacy when Combined with Gemcitabine.没食子儿茶素-3-没食子酸酯(EGCG)通过抑制 Akt 通路和上皮间质转化抑制胰腺癌细胞生长、侵袭和迁移:与吉西他滨联合使用时疗效增强。
Nutrients. 2019 Aug 9;11(8):1856. doi: 10.3390/nu11081856.