Evidence map›Paper›PMID 35626255›Full record

ArticleDiagnostics (Basel, Switzerland)2022

HLA-G 14bp Ins/Del Polymorphism, Plasma Level of Soluble HLA-G, and Association with IL-6/IL-10 Ratio and Survival of Glioma Patients.

Maria Bucova, Kristina Kluckova, Jan Kozak, Boris Rychly, Magda Suchankova, Marian Svajdler, Viktor Matejcik, Juraj Steno, Eszter Zsemlye, Vladimira Durmanova

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Association ofInternational journal of molecular sciences · 2025
    Article
  5. Article
  6. 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.

Maria BucovaFaculty of Medicine, Institute of Immunology, Comenius University, 813 72 Bratislava, Slovakia.
Kristina KluckovaFaculty of Medicine, Institute of Immunology, Comenius University, 813 72 Bratislava, Slovakia.
Jan KozakDepartment of Neurosurgery, Faculty of Medicine, Comenius University and University Hospital, 833 05 Bratislava, Slovakia.
Boris RychlyAlpha Medical, Ltd., 841 01 Bratislava, Slovakia.
Magda SuchankovaFaculty of Medicine, Institute of Immunology, Comenius University, 813 72 Bratislava, Slovakia.
Marian SvajdlerCytopathos Ltd., 831 03 Bratislava, Slovakia.ORCID 0000-0001-8052-4741
Viktor MatejcikDepartment of Neurosurgery, Faculty of Medicine, Comenius University and University Hospital, 833 05 Bratislava, Slovakia.
Juraj StenoDepartment of Neurosurgery, Faculty of Medicine, Comenius University and University Hospital, 833 05 Bratislava, Slovakia.
Eszter ZsemlyeFaculty of Medicine, Institute of Immunology, Comenius University, 813 72 Bratislava, Slovakia.
Vladimira DurmanovaFaculty of Medicine, Institute of Immunology, Comenius University, 813 72 Bratislava, Slovakia.

Funding

Comenius University grants UK 252/2018 and UK 299/2019Slovak non-profit organization League against Cancer (LPR; 2018) Z/2018/1079/VIII/LF/017
6 · The paper itself

Abstract

HLA-G is an immune checkpoint molecule with immunosuppressive and anti-inflammatory activities, and its expression and level of its soluble form (sHLA-G) may play an important role in tumor prognosis. The HLA-G 14bp ins/del polymorphism and the plasma level of soluble HLA-G (sHLA-G) were investigated by a polymerase chain reaction and ELISA, respectively, in 59 glioma patients. A significantly higher proportion of glioma patients had the 14 nt insert in both homozygous and heterozygous states compared to the control group. Glioma patients also had higher plasma levels of sHLA-G. Patients with methylated MGMT promoters had lower levels of sHLA-G than those with unmethylated MGMT promoters. The level of sHLA-G negatively correlated with the overall survival of patients. Glioblastoma patients who survived more than one year after diagnosis had lower levels of sHLA-G than those surviving less than one year. Patients with sHLA-G levels below the cut-off value of 40 U/mL survived significantly longer than patients with sHLA-G levels above 40 U/mL. The levels of sHLA-G were also negatively correlated with the level of IL-6 (

Indexed as

gliomaHLA-GIL-6polymorphismprognosissurvival

Identifiers

PMID35626255
PMCPMC9139224

What Socratic holds

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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 Socratic graph.