Novel positioning from obesity to cancer: FTO, an m


Journal

Journal of cancer research and clinical oncology
ISSN: 1432-1335
Titre abrégé: J Cancer Res Clin Oncol
Pays: Germany
ID NLM: 7902060

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 23 06 2018
accepted: 13 11 2018
pubmed: 23 11 2018
medline: 29 1 2019
entrez: 23 11 2018
Statut: ppublish

Résumé

The fat mass- and obesity-associated (FTO) gene on chromosome 16q12.2 shows an intimate association with obesity and body mass index. Recently, research into the FTO gene and its expression product has attracted widespread interest due to the identification of FTO as an N6-methyladenosine (m6A) demethylase. FTO primarily regulates the m6A levels of downstream targets via their 3' untranslated regions. FTO not only plays a critical role in obesity-related diseases but also is involved in the occurrence, development and prognosis of many types of cancer, such as acute myeloid leukaemia, glioblastoma and breast cancer. Currently, studies indicate that FTO is a crucial component of m6A modification, it regulates cancer stem cell function, and promotes the growth, self-renewal and metastasis of cancer cells. In this review, we summarized and analysed the data regarding the structural features and biological functions of FTO as well as its association with different cancers and possible molecular mechanisms. We systematically reviewed the related literatures regarding FTO and its demethylation activity in many pathologic and physiological processes, especially in cancer-related diseases based on PubMed databases in this article. Mounting evidence indicated that FTO plays a critical role in occurrence, progression and treatment of various cancers, even acting as a cancer oncogene in acute myeloid leukaemia, research on which is no longer restricted to metabolic diseases such as obesity and diabetes. Considering FTO's critical role in many diseases, FTO may become a new promising target for the diagnosis and treatment of various diseases in the near future, especially for specific types of cancers, such as acute myeloid leukaemia, glioblastoma and breast cancer.

Identifiants

pubmed: 30465076
doi: 10.1007/s00432-018-2796-0
pii: 10.1007/s00432-018-2796-0
doi:

Substances chimiques

3' Untranslated Regions 0
N-methyladenosine CLE6G00625
Alpha-Ketoglutarate-Dependent Dioxygenase FTO EC 1.14.11.33
FTO protein, human EC 1.14.11.33
Adenosine K72T3FS567

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

19-29

Subventions

Organisme : National Natural Science Foundation of China
ID : 31201028
Organisme : National Natural Science Foundation of China
ID : 81872893
Organisme : Fundamental Research Fund for the Central Universities
ID : 21617462
Organisme : Guangzhou Science Technology and Innovation Commission
ID : 201707010099
Organisme : Provincial Undergraduates' Innovation and Entrepreneurship Training Programs
ID : 82618257
Organisme : Medical Scientific Research Foundation of Guangdong Province
ID : A2017574

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Auteurs

JiaLing Chen (J)

Department of Pathology, School of Medicine, Jinan University, Guangzhou, China.

Bin Du (B)

Department of Pathology, School of Medicine, Jinan University, Guangzhou, China. tdubin@jnu.edu.cn.

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Classifications MeSH