Evidence map›Paper›PMID 26942060›Full record

ArticleOncoimmunology

Non-classical HLA-class I expression in serous ovarian carcinoma: Correlation with the HLA-genotype, tumor infiltrating immune cells and prognosis.

Emilia Andersson, Isabel Poschke, Lisa Villabona, Joseph W Carlson, Andreas Lundqvist, Rolf Kiessling, Barbara Seliger, Giuseppe V Masucci

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

8 authors at 4 institutions in 5 countries.

Emilia AnderssonDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital ; Stockholm, Sweden.
Isabel PoschkeDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden; Division of Molecular Oncology of Gastrointestinal Tumors; German Cancer Research Center; Heidelberg, Germany.
Lisa VillabonaDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital ; Stockholm, Sweden.
Joseph W CarlsonDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital ; Stockholm, Sweden.
Andreas LundqvistDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital ; Stockholm, Sweden.
Rolf KiesslingDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital ; Stockholm, Sweden.
Barbara SeligerInstitute of Medical Immunology; Martin Luther University Halle-Wittenberg ; Halle/Saale, Germany.
Giuseppe V MasucciDepartment Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital ; Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SEGerman Cancer Research Center · DEInstitute of Immunology · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In our previous studies, we have shown that patients with serous ovarian carcinoma in advanced surgical stage disease have a particularly poor prognosis if they carry the HLA-A*02 genotype. This represent a stronger prognostic factor than loss or downregulation of the MHC class I heavy chain (HC) on tumor cells. In this study, we investigated the expression of the non-classical, immune tolerogenic HLA -G and -E on the tumor cells along with the infiltration of immune cells in the tumor microenvironment. FFPE primary tumors from 72 patients with advanced stages of serous adenocarcinoma and metastatic cells present in ascites fluid from 8 additional patients were included in this study. Both expression of HLA-G and aberrant expression of HLA-E were correlated to a significant worse prognosis in patients with HLA-A*02, but not with different HLA genotypes. Focal cell expression of HLA-G correlated to a site-specific downregulation of classical MHC class I HC products and aberrant HLA-E expression, showing a poor survival. HLA-G was more frequently expressed in metastatic cells than in primary tumor lesions and the expression of HLA-G inversely correlated with the frequency of tumor infiltrating immune cells. All these parameters can contribute together to identify and discriminate subpopulations of patients with extremely poor prognosis and can give them the opportunity to receive, and benefit of individually tailored treatments.

Indexed as

HLA-A*02HLA-EHLA-Gimmunohistochemistryovarian cancerprognosisserous adenocarcinoma

Identifiers

PMID26942060
PMCPMC4760332
OpenAlexW2252529546

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.