Evidence map›Paper›PMID 28052019›Full record

ArticleOncotarget2017

TLR-activated plasmacytoid dendritic cells inhibit breast cancer cell growth in vitro and in vivo.

Jing Wu, Shuang Li, Yang Yang, Shan Zhu, Mingyou Zhang, Yuan Qiao, Yong-Jun Liu, Jingtao Chen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

39 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
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  12. Plasmacytoid Dendritic Cells as a Novel Cell-Based Cancer Immunotherapy.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Review
  15. Frontiers in genetics · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Plasmacytoid dendritic cells in the eye.Progress in retinal and eye research · 2021
    Review
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 2 institutions in 2 countries.

Jing WuInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
Shuang LiInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
Yang YangInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
Shan ZhuInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
Mingyou ZhangDepartment of Cardiovascular Center, The First Hospital, Jilin University, Changchun, 130031, China.
Yuan QiaoInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
Yong-Jun LiuInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
Jingtao ChenInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, 130061, China.
First Hospital of Jilin University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDCs) are a unique subset of naturally occurring dendritic cells, which triggers the production of large amounts of type I interferons (IFNs) after viral infections through Toll-like receptor (TLR) 7 and TLR9. Recent studies have demonstrated that the activation of pDCs kills melanoma cells. However, the role of activated pDCs in breast cancer remains to be determined. In the present study, we generated mouse models of breast cancer and demonstrated that activated pDCs can directly kill breast tumor cells through TRAIL and Granzyme B. Furthermore, we established that pDCs initiate the sequential activation of NK cells and CD8+ T cells, and ultimately inhibit breast tumor growth. Understanding the role of activated pDCs in breast cancer may help to develop new strategies for manipulating the function of pDCs and induce anti-tumor immunity in breast cancer.

Indexed as

AminoquinolinesAnimalsDendritic CellsDisease Models, AnimalFemaleGranzymesImiquimodImmunotherapy, AdoptiveInterferon InducersMammary Neoplasms, ExperimentalMembrane GlycoproteinsMiceMice, Inbred BALB CTNF-Related Apoptosis-Inducing LigandToll-Like Receptor 7Toll-Like Receptor 9AminoquinolinesGranzymesGzmb protein, mouseImiquimodInterferon InducersMembrane GlycoproteinsTlr7 protein, mouseTlr9 protein, mouseTNF-Related Apoptosis-Inducing LigandTnfsf10 protein, mouseToll-Like Receptor 7Toll-Like Receptor 9breast cancerCpGImiquimodplasmacytoid dendritic cellsToll-like receptor

Identifiers

PMID28052019
PMCPMC5355297
OpenAlexW2563407439

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.