Evidence map›Paper›PMID 34235049›Full record

ArticleJournal of bone oncology2021

Evaluation of local and circulating osteopontin in malignant and benign primary bone tumors.

Ali Nazarizadeh, Shahin Alizadeh-Fanalou, Ameinh Hosseini, Alireza Mirzaei, Vahid Salimi, Hadi Keshipour, Banafsheh Safizadeh, Khodamorad Jamshidi, Mehrdad Bahrabadi, Masoumeh Tavakoli-Yaraki

Open access · goldAbstract read
In one paragraph

Article in Journal of bone oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Ali NazarizadehDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Shahin Alizadeh-FanalouDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Ameinh HosseiniDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Alireza MirzaeiBone and Joint Reconstruction Research Center, Shafa Orthopedic Hospital, Iran University of Medical Sciences, Tehran, Iran.
Vahid SalimiDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Hadi KeshipourDepartment of Epidemiology, Faculty of Veterinary Sciences, University of Tehran, Tehran, Iran.
Banafsheh SafizadehDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Khodamorad JamshidiBone and Joint Reconstruction Research Center, Shafa Orthopedic Hospital, Iran University of Medical Sciences, Tehran, Iran.
Mehrdad BahrabadiBone and Joint Reconstruction Research Center, Shafa Orthopedic Hospital, Iran University of Medical Sciences, Tehran, Iran.
Masoumeh Tavakoli-YarakiDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Iran University of Medical Sciences · IRTehran University of Medical Sciences · IRUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe development of novel and efficient biomarkers for primary bone cancers is of grave importance.

methodsThe expression pattern of osteopontin (OPN) was investigated in the 153 patients with benign (n = 72) and malignant (n = 81) primary bone cancers. Both local and circulating OPN mRNA expression levels and their protein concentration in serum and tumor site were assessed using real-time qRT-PCR, ELISA, and immunohistochemistry techniques, respectively. As a control, 29 healthy individuals were considered. The number of 153 tumor tissue specimens and the 153 paired margins were taken on surgical resection from the patients. 153 blood samples were also drained from all participants, then peripheral blood mononuclear cells (PBMC) and sera were separated.

resultsThe mean mRNA expression was significantly higher in all of the cancerous tissues than the paired margins and the PBMC of the patients than the controls. Consistently, the protein concentrations of OPN in serum and tumor tissues were significantly higher in the patients. Furthermore, the malignant cases had significantly elevated the mRNA levels and the protein compared to the benign cases. OPN could potentially differentiate the patients from the controls with 100% sensitivity and specificity in serum. Moreover, OPN could predict some of the malignant cases' clinicopathological features, including metastasis, recurrence, grade, and response to chemotherapy.

conclusionsIn conclusion, OPN might be involved in the pathogenesis of primary bone tumors and can be considered as a potential biomarker to bone cancer diagnosis.

Indexed as

ANOVA, One-way analysis of varianceAUC, area under the curveBone tumorscDNA, Complementary DNAChondrosarcomaCI, confidence intervalDAPI, 4′,6-Diamidine-2′-phenylindole dihydrochlorideELISA, Enzyme-linked immunosorbent assayEMT, epithelial-mesenchymal transitionEwing SarcomaHIF-1α, hypoxia-inducible factor-1 alphaHRP, horseradish peroxidaseMMP9, Matrix metallopeptidase 9OCT, Optimal Cutting TemperatureOPN, OsteopontinOsteopontinOsteosarcomaPBMC, Peripheral blood mononuclear cellsPBS, phosphate-buffered salineqRT-PCR, Quantitative Real-time transcription-polymerase chain reactionROC, receiver operating characteristicS100A8, S100 calcium-binding protein A8SOX9, SRY-Box Transcription Factor 9

Identifiers

PMID34235049
PMCPMC8246632
OpenAlexW3177061652

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.