Evidence map›Paper›PMID 25785839›Full record

ArticlePloS one2015

Human malignant melanoma-derived progestagen-associated endometrial protein immunosuppresses T lymphocytes in vitro.

Suping Ren, Lina Chai, Chunyan Wang, Changlan Li, Qiquan Ren, Lihua Yang, Fumei Wang, Zhixin Qiao, Weijing Li, Min He and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
0.3field-weighted citation impact, top 41% 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, 16 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Suping RenDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Lina ChaiDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Chunyan WangDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China; Department of poisoning treatment, Beijing 307 hospital, Beijing, China.
Changlan LiDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Qiquan RenPeople's Hospital of Anqiu City, Anqiu, Shandong, China.
Lihua YangPeople's Hospital of Anqiu City, Anqiu, Shandong, China.
Fumei WangPeople's Hospital of Anqiu City, Anqiu, Shandong, China.
Zhixin QiaoDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Weijing LiDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Min HeDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Adam I RikerAdvocate Christ Medical Center, Advocate Cancer Institute, Oak Lawn, IL, United States of America.
Ying HanDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Qun YuDepartment of Immunohematology, Beijing Institute of Transfusion Medicine, Beijing, China.
Zhangqiu City People's Hospital · CN307th Hospital of Chinese People’s Liberation Army · CNAdvocate Christ Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progestagen-associated endometrial protein (PAEP) is a glycoprotein of the lipocalin family that acts as a negative regulator of T cell receptor-mediated activation. However, the function of tumor-derived PAEP on the human immune system in the tumor microenvironment is unknown. PAEP is highly expressed in intermediate and thick primary melanomas (Breslow's 2.5mm or greater) and metastatic melanomas, correlating with its expression in daughter cell lines established in vitro. The current study investigates the role of melanoma cell-secreted PAEP protein in regulating T cell function. Upon the enrichment of CD3+, CD4+ and CD8+ T cells from human peripheral blood mononuclear cells, each subset was then mixed with either melanoma-derived PAEP protein or PAEP-poor supernatant of gene-silenced tumor cells. IL-2 and IFN-γ secretion of CD4+ T cells significantly decreased with the addition of PAEP-rich supernatant. And the addition of PAEP-positive cell supernatant to activated lymphocytes significantly inhibited lymphocyte proliferation and cytotoxic T cell activity, while increasing lymphocyte apoptosis. Our result suggests that melanoma cell-secreted PAEP protein immunosuppresses the activation, proliferation and cytotoxicity of T lymphocytes, which might partially explain the mechanism of immune tolerance induced by melanoma cells within the tumor microenvironment.

Indexed as

Cell Line, TumorGlycodelinGlycoproteinsHumansInterferon-gammaInterleukin-2Lymphocyte ActivationMelanomaT-Lymphocytes, Helper-InducerGlycodelinGlycoproteinsInterferon-gammaInterleukin-2PAEP protein, human

Identifiers

PMID25785839
PMCPMC4364885
OpenAlexW2085710495

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.