Evidence map›Paper›PMID 22258792›Full record

ArticleCancer immunology, immunotherapy : CII2012

Correlation of HLA-A02* genotype and HLA class I antigen down-regulation with the prognosis of epithelial ovarian cancer.

Emilia Andersson, Lisa Villabona, Kjell Bergfeldt, Joseph W Carlson, Soldano Ferrone, Rolf Kiessling, Barbara Seliger, Giuseppe V Masucci

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

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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

25 citing papers in PubMed, 40 citations in OpenAlex.

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  20. MicroRNA-17 promotes normal ovarian cancer cells to cancer stem cells development via suppression of the LKB1-p53-p21/WAF1 pathway.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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 3 countries.

Emilia AnderssonDepartment of Oncology-Pathology, Karolinska Institute, Radiumhemmet, Karolinska University Hospital, Stockholm, Sweden.
Lisa Villabona
Kjell Bergfeldt
Joseph W Carlson
Soldano Ferrone
Rolf Kiessling
Barbara Seliger
Giuseppe V Masucci
Karolinska Institutet · SEKarolinska University Hospital · SEMartin Luther University Halle-Wittenberg · DEUniversity of Pittsburgh · US

Funding

HLA Expression in CancerR03TW005900 · FIC · ROSWELL PARK CANCER INSTITUTE CORP · PI FERRONE, SOLDANO · 2004 to 2006
$95k
FIC NIH HHS R03 TW005900
6 · The paper itself

Abstract

backgroundIn recent years, evidence is accumulating that cancer cells develop strategies to escape immune recognition. HLA class I HC down-regulation is one of the most investigated. In addition, different HLA haplotypes are known to correlate to both risk of acquiring diseases and also prognosis in survival of disease or cancer. We have previously shown that patients with serous adenocarcinoma of the ovary in advanced surgical stage disease have a particularly poor prognosis if they carry the HLA-A02* genotype. We aimed to study the relationship between HLA-A02* genotype in these patients and the subsequent HLA class I HC protein product defects in the tumour tissue. MATERIALS AND

methodsOne hundred and sixty-two paraffin-embedded tumour lesions obtained from Swedish women with epithelial ovarian cancer were stained with HLA class I heavy chain (HC) and β(2)-microglobulin (β(2)-m)-specific monoclonal antibodies (mAb). Healthy ovary and tonsil tissue served as a control. The HLA genotype of these patients was determined by PCR/sequence-specific primer method. The probability of survival was calculated using the Kaplan-Meier method, and the hazard ratio (HR) was estimated using proportional hazard regression.

resultsImmunohistochemical staining of ovarian cancer lesions with mAb showed a significantly higher frequency of HLA class I HC and β(2)-m down-regulation in patients with worse prognosis (WP) than in those with better prognosis. In univariate analysis, both HLA class I HC down-regulation in ovarian cancer lesions and WP were associated with poor survival. In multivariate Cox-analysis, the WP group (all with an HLA-A02* genotype) had a significant higher HR to HLA class I HC down-regulation.

conclusionsHLA-A02* is a valuable prognostic biomarker in epithelial ovarian cancer. HLA class I HC loss and/or down-regulation was significantly more frequent in tumour tissues from HLA-A02* positive patients with serous adenocarcinoma surgical stage III-IV. In multivariate analysis, we show that the prognostic impact is reasonably correlated to the HLA genetic rather than to the expression of its protein products.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAged, 80 and overbeta 2-MicroglobulinBiomarkers, TumorCarcinoma, Ovarian EpithelialDown-RegulationFemaleGenotypeHistocompatibility Antigens Class IHLA-A2 AntigenHumansImmunohistochemistryKaplan-Meier EstimateMiddle Agedbeta 2-MicroglobulinBiomarkers, TumorHistocompatibility Antigens Class IHLA-A2 Antigen

Identifiers

PMID22258792
PMCPMC8693725
OpenAlexW1980094840

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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.