Evidence map›Paper›PMID 34250760›Full record

ArticleCancer medicine2021

Diagnostic and prognostic value of stem cell factor plasma level in glioblastoma multiforme patients.

Amirhosein Kefayat, Alireza Amouheidari, Fatemeh Ghahremani, Zahra Alirezaei

Abstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Amirhosein KefayatDepartment of Oncology, Isfahan University of Medical Sciences, Isfahan, Iran.ORCID 0000-0002-0616-8870
Alireza AmouheidariDepartment of Radiation Oncology, Isfahan Milad Hospital, Isfahan, Iran.ORCID 0000-0001-5329-9438
Fatemeh GhahremaniDepartment of Medical Physics and Radiotherapy, School of Paramedicine, Arak University of Medical Sciences, Arak, Iran.ORCID 0000-0002-7244-6066
Zahra AlirezaeiDepartment of Medical Physics and Radiotherapy, Isfahan University of Medical Sciences, Isfahan, Iran.

Funding

Arak University of Medical Sciences 3428
6 · The paper itself

Abstract

backgroundInvestigation of novel blood-circulating agents as potential biomarkers for glioblastoma multiforme (GBM) patients' diagnosis and monitoring has gained lots of attention, due to limitations of imaging modalities and invasive tissue biopsy procedures. The present study aims to assess the diagnostic and prognostic values of preoperative stem cell factor (SCF) plasma level in GBM patients.

methodsPreoperative plasma samples from 58 GBM patients and 20 patients with nonglial tumors and 30 healthy controls were obtained. SCF levels were measured by employing the enzyme-linked immunosorbent assay test and the values were compared between these three groups. Then, the association of SCF plasma level and tumor volume, progression-free survival (PFS), and overall survival (OS) for the GBM patients were evaluated.

resultsMean preoperative SCF plasma level of the GBM patients (2.80 ± 1.52 ng/ml) was significantly higher (p < 0.0001) than the healthy controls (0.80 ± 0.24 ng/ml) and patients with nonglial tumor (1.41 ± 0.76 ng/ml). Receiver operating characteristic analysis revealed that the preoperative SCF plasma level could distinguish the GBM patients from healthy controls and patients with nonglial tumors with the area under curve values of 0.915 and 0.790, respectively. However, no significant association was observed between the GBM patients' preoperative SCF plasma levels and tumors' volume (Spearman Rho correlation coefficient, 0.1847; 95% CI, p = 0.1652). The GBM patients were divided into two subgroups based on mean preoperative SCF plasma levels (2.80 ng/ml). No significant difference was observed between the patients' PFS (p = 0.3792) and OS (p = 0.1469) at these two subgroups.

conclusionTaking together, the SCF plasma level can serve as a novel diagnostic blood-circulating biomarker for patients with GBM. However, its plasma level is not correlated with GBM patients' tumor volume, PFS, or OS.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBrain NeoplasmsCase-Control StudiesDiagnosis, DifferentialDNA Modification MethylasesDNA Repair EnzymesEnzyme-Linked Immunosorbent AssayFemaleGlioblastomaHumansIsocitrate DehydrogenaseMaleMethylationBiomarkers, TumorDNA Modification MethylasesDNA Repair EnzymesIDH1 protein, humanIDH2 protein, humanIsocitrate DehydrogenaseMGMT protein, humanStem Cell FactorTumor Suppressor Proteinsbiomarkerc-Kitdiagnosisglioblastoma multiformeprognosisstem cell factor

Identifiers

PMID34250760
PMCPMC8335833

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