Literature DB >> 24100923

FTY720 for cancer therapy (Review).

Li Zhang1, Han-Dong Wang, Xiang-Jun Ji, Zi-Xiang Cong, Jian-Hong Zhu, Yuan Zhou.   

Abstract

2-Amino-2-[2-(4-octylphenyl)]-1,3-propanediol hydrochloride (FTY720) is a potent immunosuppressant which has been approved by the Food and Drug Administration (FDA) as a new treatment for multiple sclerosis. As an immunosuppressant, it displays its anti-multiple sclerosis, immunosuppressive effects by activating sphingosine-1-phosphate receptors (S1PRs). In addition to the immunosuppressive effects, FTY720 also shows preclinical antitumor efficacy in several cancer models. In most cases, phosphorylation of FTY720 is not required for its cytotoxic effect, indicating the involvement of S1PR-independent mechanisms which are starkly different from the immunosuppressive property of FTY720. In the present study, we reviewed the rapidly advancing field of FTY720 in cancer therapy as well as some molecular targets of the unphosphorylated form of FTY720.

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Year:  2013        PMID: 24100923     DOI: 10.3892/or.2013.2765

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  22 in total

1.  Sphingosine-1-Phosphate Receptor-1 Promotes Environment-Mediated and Acquired Chemoresistance.

Authors:  Veronica Lifshitz; Saul J Priceman; Wenzhao Li; Gregory Cherryholmes; Heehyoung Lee; Adar Makovski-Silverstein; Lucia Borriello; Yves A DeClerck; Hua Yu
Journal:  Mol Cancer Ther       Date:  2017-07-17       Impact factor: 6.261

2.  Signaling pathway involved in the inhibitory effect of FTY720P on the Na+/K+ ATPase in HepG2 cells.

Authors:  Nadine Al Alam; Sawsan Ibrahim Kreydiyyeh
Journal:  J Cell Commun Signal       Date:  2017-02-14       Impact factor: 5.782

3.  Traumatic Brain Injury-Induced Neuronal Apoptosis is Reduced Through Modulation of PI3K and Autophagy Pathways in Mouse by FTY720.

Authors:  Li Zhang; Ke Ding; Handong Wang; Yong Wu; Jianguo Xu
Journal:  Cell Mol Neurobiol       Date:  2015-06-23       Impact factor: 5.046

Review 4.  Advances in the management of peritoneal mesothelioma.

Authors:  Ali Raza; Wei-Ching Huang; Kazuaki Takabe
Journal:  World J Gastroenterol       Date:  2014-09-07       Impact factor: 5.742

5.  FTY720 reduces migration and invasion of human glioblastoma cell lines via inhibiting the PI3K/AKT/mTOR/p70S6K signaling pathway.

Authors:  Li Zhang; Handong Wang; Jianhong Zhu; Ke Ding; Jianguo Xu
Journal:  Tumour Biol       Date:  2014-07-30

Review 6.  The antineoplastic properties of FTY720: evidence for the repurposing of fingolimod.

Authors:  Sathya Narayanan Patmanathan; Lee Fah Yap; Paul G Murray; Ian C Paterson
Journal:  J Cell Mol Med       Date:  2015-07-14       Impact factor: 5.310

7.  Association of Sphingosine-1-phosphate (S1P)/S1P Receptor-1 Pathway with Cell Proliferation and Survival in Canine Hemangiosarcoma.

Authors:  A M Rodriguez; A J Graef; D N LeVine; I R Cohen; J F Modiano; J-H Kim
Journal:  J Vet Intern Med       Date:  2015-06-25       Impact factor: 3.333

8.  The phosphorylated prodrug FTY720 is a histone deacetylase inhibitor that reactivates ERα expression and enhances hormonal therapy for breast cancer.

Authors:  N C Hait; D Avni; A Yamada; M Nagahashi; T Aoyagi; H Aoki; C I Dumur; Z Zelenko; E J Gallagher; D Leroith; S Milstien; K Takabe; S Spiegel
Journal:  Oncogenesis       Date:  2015-06-08       Impact factor: 7.485

9.  In search of constrained FTY720 and phytosphingosine analogs as dual acting anticancer agents targeting metabolic and epigenetic pathways.

Authors:  Jean-Baptiste Garsi; Lorenzo Sernissi; Vito Vece; Stephen Hanessian; Alison N McCracken; Grigor Simitian; Aimee L Edinger
Journal:  Eur J Med Chem       Date:  2018-09-21       Impact factor: 6.514

Review 10.  Fingolimod for the treatment of neurological diseases-state of play and future perspectives.

Authors:  Robert Brunkhorst; Rajkumar Vutukuri; Waltraud Pfeilschifter
Journal:  Front Cell Neurosci       Date:  2014-09-12       Impact factor: 5.505

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