Evidence map›Paper›PMID 25686832›Full record

ArticleOncotarget2015

Zfra activates memory Hyal-2+ CD3- CD19- spleen cells to block cancer growth, stemness, and metastasis in vivo.

Ming-Hui Lee, Wan-Pei Su, Wan-Jen Wang, Sing-Ru Lin, Chen-Yu Lu, Yu-An Chen, Jean-Yun Chang, Shenq-Shyang Huang, Pei-Yi Chou, Siou-Ru Ye and 11 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 19 citations in OpenAlex.

  1. Zfra Overrides WWOX in Suppressing the Progression of Neurodegeneration.International journal of molecular sciences · 2024
    Review
  2. Zfra Inhibits the TRAPPC6AΔ-Initiated Pathway of Neurodegeneration.International journal of molecular sciences · 2022
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. WWOX PossessesCancers · 2019
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. HYAL-2-WWOX-SMAD4 Signaling in Cell Death and Anticancer Response.Frontiers in cell and developmental biology · 2016
    Review
  17. Article
  18. 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

21 authors at 4 institutions in 2 countries.

Ming-Hui LeeInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Wan-Pei SuInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Wan-Jen WangInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Sing-Ru LinInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Chen-Yu LuInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Yu-An ChenInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Jean-Yun ChangInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Shenq-Shyang HuangInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Pei-Yi ChouInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Siou-Ru YeInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Szu-Jung ChenInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Huan HeInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Ting-Hsiu LiuInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Ying-Tsen ChouInstitute of Basic Medical Sciences, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Li-Jin HsuDepartment of Medical Laboratory Science and Biotechnology, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Feng-Jie LaiDepartment of Dermatology, Chi-Mei Medical Center, Tainan, Taiwan, ROC.
Shean-Jen ChenAdvanced Optoelectronic Technology Center, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
Hoong-Chien LeeGraduate Institute of Systems Biology and Bioinformatics, National Central University, Zhongli, Taiwan, ROC.
David KakhniashviliInstitute of Biomedical Sciences and Technology, Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY, USA.
Steven R GoodmanInstitute of Biomedical Sciences and Technology, Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY, USA.
Nan-Shan ChangInstitute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan, ROC.
National Cheng Kung University · TWSUNY Upstate Medical University · USChi Mei Medical Center · TWNational Central University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zfra is a 31-amino-acid zinc finger-like protein, which participates in the tumor necrosis factor signaling. Here, we determined that when nude mice and BALB/c mice were pre-injected with nanogram levels of a synthetic Zfra1-31 or truncated Zfra4-10 peptide via tail veins, these mice became resistant to the growth, metastasis and stemness of melanoma cells, and many malignant cancer cells. The synthetic peptides underwent self-polymerization in phosphate-buffered saline. Alteration of the Ser8 phosphorylation site to Gly8 abolished Zfra aggregation and its-mediated cancer suppression in vivo. Injected Zfra peptide autofluoresced due to polymerization and was trapped mainly in the spleen. Transfer of Zfra-stimulated spleen cells to naïve mice conferred resistance to cancer growth. Zfra-binding cells, designated Hyal-2+ CD3- CD19- Z cells, are approximately 25-30% in the normal spleen, but are significantly downregulated (near 0-3%) in tumor-growing mice. Zfra prevented the loss of Z cells caused by tumors. In vitro stimulation or education of naïve spleen cells with Zfra allowed generation of activated Z cells to confer a memory anticancer response in naïve or cancer-growing mice. In particular, Z cells are abundant in nude and NOD-SCID mice, and can be readily activated by Zfra to mount against cancer growth.

Indexed as

Adaptor Proteins, Signal TransducingAmino Acid SequenceAnimalsAntigens, CD19CD3 ComplexCell Adhesion MoleculesGPI-Linked ProteinsHumansHyaluronoglucosaminidaseMaleMiceMice, Inbred BALB CMice, Inbred NODMice, NudeMice, SCIDMolecular Sequence DataAdaptor Proteins, Signal TransducingAntigens, CD19APBB2 protein, humanCD3 ComplexCell Adhesion MoleculesGPI-Linked ProteinsHyal2 protein, humanHyal2 protein, mouseHyaluronoglucosaminidasePeptide Fragments

Identifiers

PMID25686832
PMCPMC4414150
OpenAlexW1534770787

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.