Evidence map›Paper›PMID 27027355›Full record

ArticleOncotarget2016

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, Miao Cui, Guanglin Bian, Feihong Xu, David Chiang and 14 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Oxaliplatin Treatment Alters Systemic Immune Responses.BioMed research international · 2019
    Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 6 institutions in 2 countries.

Juan WangGuangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Liang PengDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ruihua ZhangDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Zihan ZhengDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Chun ChenAmgen Inc., Thousand Oaks, CA, USA.
Ka Lung CheungDepartment of Structural and Chemical Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Miao CuiDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Guanglin BianDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Feihong XuDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
David ChiangDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Yuan HuDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ye ChenGuangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Geming LuDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jianjun YangDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Hui ZhangDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jianfei YangTempero Pharmaceuticals, GlasxoSmithKline, Cambridge, MA, USA.
Hongfa ZhuDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Shu-Hsia ChenDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Kebin LiuDepartment of Biochemistry and Molecular Biology, Medical College of Georgia, Georgia Regents University, Augusta, GA, USA.
Ming-Ming ZhouDepartment of Structural and Chemical Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Andrew G SikoraDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Liwu LiDepartment of Biological Sciences, Virginia Tech, Blacksburg, VA, USA.
Bo JiangGuangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Huabao XiongDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · USSouthern Medical University · CNAmgen (United States) · USAugusta University · USNanfang Hospital · CNVirginia Tech · US

Funding

THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSEP01DK072201 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HARPAZ, NOAM · 2006 to 2015
$14.6M
Intervention of immune tolerance by small molecules to enhance immune therapyR01CA127483 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, SHU-HSIA · 2008 to 2018
$3.4M
Myeloid Suppressor Cell-Mediated Immune Suppression of Tumor Specific T CellsR01CA109322 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, SHU-HSIA · 2006 to 2015
$3.2M
Role of IRF8 in Tumor Rejection and SuppressionR01CA133085 · NCI · AUGUSTA UNIVERSITY · PI LIU, KEBIN · 2008 to 2019
$2.9M
T cell-derived iNOS switches off TH17 cell differentiation in inflammationR01AI104688 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI XIONG, HUABAO · 2013 to 2016
$1.7M
Silencing of Th17 cell differentiation by IRF8 in the development of colitisR56AI091871 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI XIONG, HUABAO · 2011 to 2011
$424k
NCI NIH HHS R01 CA109322NCI NIH HHS R01 CA127483NCI NIH HHS R01 CA133085NIAID NIH HHS R01 AI104688NIAID NIH HHS R56 AI091871NIDDK NIH HHS P01 DK072201
6 · The paper itself

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.

Indexed as

AnimalsAntimetabolites, AntineoplasticBlotting, WesternCell DifferentiationCell Line, TumorColitisCytokinesDose-Response Relationship, DrugFluorouracilMice, Inbred C57BLMice, KnockoutReverse Transcriptase Polymerase Chain ReactionRNA InterferenceTh17 CellsTh1 CellsThymidylate SynthaseAntimetabolites, AntineoplasticCytokinesFluorouracilThymidylate Synthase5-FUImmune responseImmunityImmunology and Microbiology SectionTH17TS

Identifiers

PMID27027355
PMCPMC4991385
OpenAlexW2305868841

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.