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5-Fluorouracil targets thymidylate synthase in the selective suppression of TH17 cell differentiation

  • Juan Wang
    ,
  • Liang Peng
    ,
  • Ruihua Zhang
    ,
  • Zihan Zheng
    ,
  • Chun Chen
    ,
  • Ka Lung Cheung
*Corresponding author for this work
  • Icahn School of Medicine at Mount Sinai
    ,
  • Southern Medical University
    ,
  • University of North Carolina at Chapel Hill
    ,
  • Virginia Polytechnic Institute and State University
    ,
  • Amgen Incorporated
    ,
  • Tempero Pharmaceuticals
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

While it is well established that treatment of cancer patients with 5-Fluorouracil (5-FU) can result in immune suppression, the exact function of 5-FU in the modulation of immune cells has not been fully established. We found that low dose 5-FU selectively suppresses TH17 and TH1 cell differentiation without apparent effect on Treg, TH2, and significantly suppresses thymidylate synthase (TS) expression in TH17 and TH1 cells but has a lesser effect in tumor cells and macrophages. Interestingly, the basal expression of TS varies significantly between T helper phenotypes and knockdown of TS significantly impairs TH17 and TH1 cell differentiation without affecting the differentiation of either Treg or TH2 cells. Finally, low dose 5-FU is effective in ameliorating colitis development by suppressing TH17 and TH1 cell development in a T cell transfer colitis model. Taken together, the results highlight the importance of the anti-inflammatory functions of low dose 5-FU by selectively suppressing TH17 and TH1 immune responses.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 19312-19326 (15 pages)

Journal (Volume, Issue Number)

Oncotarget (Volume 7, Issue 15)

Publication milestones

  • Published - 04/12/2016

Publication status

Published - 04/12/2016

ISSN

1949-2553

Publication IDs

  • Scopus: 84964727150
  • PubMed: 27027355

Publication metrics

Metrics

Scopus
citations
SciVal
citations
8
SciVal
FWCI
0.46
SciVal
Author count
24
SciVal
Paper percentile
67
Fractional count
1
Fractional count
0.04
Fractional count
23
Fractional count
0.96
Fractional count
1
Fractional count
1

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Citation count
16
Social media
1
Captures
30

Funding Details

FunderFunding number
NIAID
R01AI104688