Evidence map›Paper›PMID 31491449›Full record

ArticleCancer letters2019

Progranulin promotes melanoma progression by inhibiting natural killer cell recruitment to the tumor microenvironment.

Ramouna Voshtani, Mei Song, Huan Wang, Xiaoqi Li, Wei Zhang, Mojdeh S Tavallaie, Wenjun Yan, Joseph Sun, Fang Wei, Xiaojing Ma

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. KIR2DS2 Expression Identifies NK Cells With Enhanced Anticancer Activity.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  8. Review
  9. Autophagy in the Neuronal Ceroid Lipofuscinoses (Batten Disease).Frontiers in cell and developmental biology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
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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

10 authors at 4 institutions in 2 countries.

Ramouna VoshtaniState Key Laboratory of Microbial Metabolism, Sheng Yushou Center of Cell Biology and Immunology, School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai, China.
Mei SongDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, USA.
Huan WangState Key Laboratory of Microbial Metabolism, Sheng Yushou Center of Cell Biology and Immunology, School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai, China.
Xiaoqi LiState Key Laboratory of Microbial Metabolism, Sheng Yushou Center of Cell Biology and Immunology, School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai, China.
Wei ZhangState Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Mojdeh S TavallaieDepartment of Pharmaceutical Sciences, Shanghai Jiaotong University, Shanghai, 200240, China.
Wenjun YanState Key Laboratory of Microbial Metabolism, Sheng Yushou Center of Cell Biology and Immunology, School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai, China.
Joseph SunImmunology Program, Memorial Sloan-Kettering Cancer Center, New York, USA.
Fang WeiState Key Laboratory of Microbial Metabolism, Sheng Yushou Center of Cell Biology and Immunology, School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai, China. Electronic address: fangwei@sjtu.edu.cn.
Xiaojing MaState Key Laboratory of Microbial Metabolism, Sheng Yushou Center of Cell Biology and Immunology, School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai, China; Department of Microbiology and Immunology, Weill Cornell Medicine, New York, USA. Electronic address: xim2002@sjtu.edu.cn.
Shanghai Jiao Tong University · CNCornell University · USMemorial Sloan Kettering Cancer Center · USRenji Hospital · CN

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Mechanism of Progranulin-mediated control of septic inflammation via IL-10R56AI103157 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MA, XIAOJING · 2014 to 2014
$424k
Regulation of IL-10 Gene Expression and Host Septic Response by ProgranulinR56AI095512 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MA, XIAOJING · 2011 to 2011
$254k
NCI NIH HHS P30 CA008748NIAID NIH HHS R56 AI095512NIAID NIH HHS R56 AI103157
6 · The paper itself

Abstract

Progranulin (PGRN) is a growth factor with significant biological effects in different types of cancer. However, its role in melanoma progression has not been explored. In this study, we first analyze clinical datasets and show that high PGRN expression levels are correlated with poor prognosis of melanoma patients. Further, we demonstrate in a transplanted murine melanoma model in which the endogenous Grn gene encoding PGRN has been deleted that tumor-derived, not host-derived PGRN, promotes melanoma growth and metastasis. Immunological analyses reveal an enhanced infiltration of natural killer cells, but not T lymphocytes, into PGRN-deficient tumors compared to the wild type control. Antibody-mediated depletion confirms the critical role of NK cells in controlling B16 tumor growth. RNA-seq analysis reveals that several chemokines including CCL5 are strongly upregulated in PGRN-deficient tumor. Silencing CCL5 expression in PGRN-deficient tumor reduces NK cell recruitment and restores tumor growth to the control level. Lastly, we show that PGRN inhibits Ccl5 gene expression at the transcriptional level. This study highlights a novel and critical role of PGRN in melanoma growth and metastasis and suggests that it may represent a potential therapeutic target.

Indexed as

Up-RegulationAnimalsCell Line, TumorCell ProliferationChemokine CCL5Disease ProgressionFemaleGene Expression Regulation, NeoplasticHumansKiller Cells, NaturalMelanomaMiceNeoplasm MetastasisNeoplasm TransplantationPrognosisProgranulinsCCL5 protein, humanChemokine CCL5GRN protein, humanProgranulinsCCL5Immune responseMelanomaNatural killer cellProgranulin

Identifiers

PMID31491449
PMCPMC7519469
OpenAlexW2971444951

What OpenQuestion holds

Textmetadata
LicenceTDM
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.