Evidence map›Paper›PMID 25701137›Full record

ArticleCancer biology & therapy2015

Methionine enkephalin (MENK) inhibits tumor growth through regulating CD4+Foxp3+ regulatory T cells (Tregs) in mice.

Xuan Li, Yiming Meng, Nicolas P Plotnikoff, Gene Youkilis, Noreen Griffin, Enhua Wang, Changlong Lu, Fengping Shan

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. B-Cell Depletion with CD20 Antibodies as New Approach in the Treatment of Inflammatory and Immunological Events Associated with Spinal Cord Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    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

8 authors at 3 institutions in 2 countries.

Xuan Lia Department of Immunology, School of Basic Medical Science , China Medical University , Shenyang , PR, China.
Yiming Meng
Nicolas P Plotnikoff
Gene Youkilis
Noreen Griffin
Enhua Wang
Changlong Lu
Fengping Shan
China Medical University · CNOrlando Immunology Center · USOrlando Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methionine enkephalin (MENK), an endogenous neuropeptide, plays an crucial role in both neuroendocrine and immune systems. CD4+Foxp3+ regulatory T cells (Tregs) are identified as a major subpopulation of T lymphocytes in suppressing immune system to keep balanced immunity. The aim of this research work was to elucidate the mechanisms via which MENK interacts with Tregs in cancer situation. The influence of MENK on transforming growth factor-β (TGF-β) mediated conversion from naïve CD4+CD25- T cells to CD4+CD25+ Tregs was determined and the data from flow cytometry (FCM) analysis indicated that MENK effectively inhibited the expression of Foxp3 during the process of TGF-βinduction. Furthermore, this inhibiting process was accompanied by diminishing phosphorylation and nuclear translocation of Smad2/3, confirmed by western blot (WB) analysis and immunofluorescence (IF) at molecular level. We established sarcoma mice model with S180 to investigate whether MENK could modulate Tregs in tumor circumstance. Our findings showed that MENK delayed the development of tumor in S180 tumor bearing mice and down-regulated level of Tregs. Together, these novel findings reached a conclusion that MENK could inhibit Tregs activity directly and retard tumor development through down-regulating Tregs in mice. This work advances the deepening understanding of the influence of MENK on Tregs in cancer situation, and relation of MENK with immune system, supporting the implication of MENK as a new strategy for cancer immunotherapy.

Indexed as

ImmunotherapyAnimalsCD4-Positive T-LymphocytesCell Line, TumorCell ProliferationEnkephalin, MethionineFlow CytometryForkhead Transcription FactorsHumansMiceSarcomaT-Lymphocytes, RegulatoryTransforming Growth Factor betaEnkephalin, MethionineForkhead Transcription FactorsFoxp3 protein, mouseTransforming Growth Factor betacancer immunoregulationCCR4, CC chemokine receptor 4CTLA-4, cytotoxic T Lymphocyte Antigen-4FasL, Fas ligandFCM, flow cytometryforkhead box P3 transcription factorFoxp3, forkhead box P3 transcription factorGITR, glucocorticoid-induced TNFRIF, immunofluorescenceIL-2, interleukin-2MENK, methionine enkephalinmethionine enkephalinMFI, median fluorescence intensityMTS, 3-(4, 5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner saltreal-time PCR, real-time polymerase chain reactionregulatory T cell reprogrammingregulatory T cellsSmad2/3 proteinTGF-β,transforming growth factor-βtransforming growth factor-βTregs, regulatory T cellsWB, protein gel blot

Identifiers

PMID25701137
PMCPMC4622478
OpenAlexW1724099110

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.