Evidence map›Paper›PMID 29322326›Full record

ArticleHistochemistry and cell biology2018

Heparan sulfate accumulation and perlecan/HSPG2 up-regulation in tumour tissue predict low relapse-free survival for patients with glioblastoma.

Galina M Kazanskaya, Alexandra Y Tsidulko, Alexander M Volkov, Roman S Kiselev, Anastasia V Suhovskih, Vyacheslav V Kobozev, Alexei S Gaytan, Svetlana V Aidagulova, Alexei L Krivoshapkin, Elvira V Grigorieva

Abstract read
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In one paragraph

Article in Histochemistry and cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Frontiers in cell and developmental biology · 2026
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  3. Microenvironmental Drivers of Glioma Progression.International journal of molecular sciences · 2025
    Review
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  11. Cancers · 2022
    Article
  12. Article
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  19. Article
  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

10 authors at 4 institutions in 1 country.

Galina M KazanskayaInstitute of Molecular Biology and Biophysics, Timakova 2/12, Novosibirsk, 630117, Russia.
Alexandra Y TsidulkoInstitute of Molecular Biology and Biophysics, Timakova 2/12, Novosibirsk, 630117, Russia.
Alexander M VolkovMeshalkin National Medical Research Center, Novosibirsk, Russia.
Roman S KiselevMeshalkin National Medical Research Center, Novosibirsk, Russia.
Anastasia V SuhovskihInstitute of Molecular Biology and Biophysics, Timakova 2/12, Novosibirsk, 630117, Russia.
Vyacheslav V KobozevMeshalkin National Medical Research Center, Novosibirsk, Russia.
Alexei S GaytanNovosibirsk State Medical University, Novosibirsk, Russia.
Svetlana V AidagulovaNovosibirsk State Medical University, Novosibirsk, Russia.
Alexei L KrivoshapkinNovosibirsk State Medical University, Novosibirsk, Russia.
Elvira V GrigorievaInstitute of Molecular Biology and Biophysics, Timakova 2/12, Novosibirsk, 630117, Russia. elv_grig@yahoo.com.
Novosibirsk State Medical University · RUInstitute of Molecular Biology and Biophysics · RUMeshalkin National Medical Research Center · RUNovosibirsk State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycosaminoglycans are major components of brain extracellular matrix (ECM), although heparan sulfate (HS) contribution in brain physiology and carcinogenesis remains underinvestigated. This study examined HS content and distribution in glioblastoma multiforme (GBM) tissues in the context of potential molecular mechanisms underlying its deregulation in brain tumours. Totally, 42 tissue samples and paraffin-embedded tissues for 31 patients with different prognosis were investigated. HS expression was demonstrated in 50-55% of the GBM tumours by immunohistochemistry (IHC), while almost no HS content was detected in the surrounding paratumourous brain tissues. Heterogeneous HS distribution in the HS-positive tumours was more related to the necrosis or glandular-like brain zones rather than glioma cells with high or low Ki-67 index. According the Kaplan-Meier curves, HS accumulation in glioma cells was associated with low relapse-free survival (RS) of the GBM patients (p < 0.05) and was likely to be due to the increased transcriptional activity of HSPG core proteins (syndecan-1, 2-3 fold; glypican-1, 2,5 fold; perlecan/HSPG2, 13-14 fold). Activation of perlecan/HSPG2 expression correlated with the patients' survival according Kaplan-Meier (p = 0.0243) and Cox proportional-hazards regression (HR = 3.1; P(Y) = 0.03) analyses, while up-regulation of syndecan-1 and glypican-1 was not associated with the patients survival. Taken together, the results indicate that increase of HS content and up-regulation of perlecan/HSPG2 expression in glioblastoma tissues contribute to tumour development through the transformation of brain extracellular matrix into tumour microenvironment, and represent negative prognostic factors for glioblastoma progression.

Indexed as

Up-RegulationBrain NeoplasmsGlioblastomaHeparan SulfateHeparan Sulfate ProteoglycansHumansMiddle AgedRecurrenceSurvival AnalysisHeparan SulfateHeparan Sulfate ProteoglycansperlecanGlioblastomaGlypican-1Heparan sulfatePerlecan/HSPG2ProteoglycanSyndecan-1

Identifiers

PMID29322326
OpenAlexW2782595700

What OpenQuestion holds

Textmetadata
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.