Evidence map›Paper›PMID 30802770›Full record

ArticleNeoplasia (New York, N.Y.)2019

High Expression of HLA-G in Ovarian Carcinomatosis: The Role of Interleukin-1β.

Matti Ullah, Dallel Azazzen, Rachid Kaci, Nadia Benabbou, Eric Pujade Lauraine, Marc Pocard, Massoud Mirshahi

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 32 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

7 authors at 1 institution in 1 country.

Matti UllahINSERM U965, Sorbonne Paris Cité-Paris Diderot University, Carcinomatosis Angiogenesis Translational Research, Hospital Lariboisière, 75010 Paris, France.
Dallel AzazzenINSERM U965, Sorbonne Paris Cité-Paris Diderot University, Carcinomatosis Angiogenesis Translational Research, Hospital Lariboisière, 75010 Paris, France.
Rachid KaciINSERM U965, Sorbonne Paris Cité-Paris Diderot University, Carcinomatosis Angiogenesis Translational Research, Hospital Lariboisière, 75010 Paris, France; Central Department of Anatomy and Pathological Cytology, Hospital Lariboisière, 75010 Paris, France.
Nadia BenabbouINSERM U965, Sorbonne Paris Cité-Paris Diderot University, Carcinomatosis Angiogenesis Translational Research, Hospital Lariboisière, 75010 Paris, France.
Eric Pujade LauraineARCAGY, Hotel Dieu, 75004, Paris.
Marc PocardINSERM U965, Sorbonne Paris Cité-Paris Diderot University, Carcinomatosis Angiogenesis Translational Research, Hospital Lariboisière, 75010 Paris, France.
Massoud MirshahiINSERM U965, Sorbonne Paris Cité-Paris Diderot University, Carcinomatosis Angiogenesis Translational Research, Hospital Lariboisière, 75010 Paris, France. Electronic address: massoud.mirshahi@inserm.fr.
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study focuses on the influence of the tumor microenvironment on the expression of HLA-G in ovarian cancer and its impact on immune cells. We used carcinomatosis fluids (n = 16) collected from patients diagnosed with epithelial ovarian cancer, detected by an increase in CA125 levels. Our results indicate that HLA-G is expressed by 1) ascitic cell clusters, 2) stromal cells (hospicells) extracted from cancer cell clusters, and 3) cancer cell lines and tumor cells. The origin of HLA-G was linked to inflammatory cytokines present in the cancer microenvironment. In parallel, the ascitic fluid of patients with ovarian cancer contains soluble HLA-G (sHLA-G). The mesothelial cell layer and submesothelial tissues, as well as the immune cell infiltrate, do not secrete HLA-G. In contrast, sHLA-G is absorbed by peritoneal tissues along with mesothelial layers as well as immune cell infiltrates. We demonstrated that interleukin-1β along with TGF-β can be a major HLA-G-inducing factor that upregulates HLA-G expression through the NF-κB pathway. The level of HLA-G in ascites correlated positively with the expression of T regulatory (T-regs) cells, while it negatively correlated with the expression of natural killer and memory cells in tumor-infiltrating immune cells. In conclusion, the production of HLA-G is associated with the presence of inflammatory cytokines and is strongly correlated with microenvironment tolerant cells such as T-regs and diminution of NK and memory T cells.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkersCarcinomaCell AdhesionCell Line, TumorCell MembraneCytokinesEnzyme-Linked Immunosorbent AssayFemaleHLA-G AntigensHumansImmunohistochemistryInterleukin-1betaLymphocytes, Tumor-InfiltratingOvarian NeoplasmsProtein BindingBiomarkersCytokinesHLA-G AntigensInterleukin-1beta

Identifiers

PMID30802770
PMCPMC6389653
OpenAlexW2916891673

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.