Evidence map›Paper›PMID 26446495›Full record

ArticleDiagnostic pathology2015

Up-regulation of miR-130b expression level and down-regulation of miR-218 serve as potential biomarker in the early detection of human osteosarcoma.

Afshin Taheriazam, Amir Jouya Talaei, Mohammad Jamshidi, Mohammadreza Shakeri, Samaneh Khoshbakht, Emad Yahaghi, Marjan Shokrani

RetractedAbstract readRetracted Publication
In one paragraph

Article in Diagnostic pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Evaluation of gene expression level of CDC5L and MACC1 in poor prognosis and progression of osteosarcoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Afshin TaheriazamDepartment of Orthopedics Surgery, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran.
Amir Jouya TalaeiDepartment of Genetics, Faculty of Life Sciences, Azad University of Tehran Medical Sciences Branch, Tehran, Iran.
Mohammad JamshidiCellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.
Mohammadreza ShakeriDepartment of Orthopaedic and Trauma Surgery, Birjand University of Medical Sciences, Birjand, Iran.
Samaneh KhoshbakhtDepartment of Statistics, Faculty of Sciences, Islamic Azad University, Mashhad Branch, Mashhad, Iran.
Emad YahaghiDepartment of Molecular Biology, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Marjan ShokraniGraduate, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran. drshokrani.tums@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is a primary malignant bone tumor with high morbidity that principally emerges in children and adolescents. MiRNAs regulate a variety of normal physiologic processes and are involved in tumorigenesis and development of multiple malignancies, including OS. This study was aimed to evaluate the clinical significance of miR-130b and miR-218 in osteosarcoma patient.

methodsWe utilized quantitative real-time PCR to evaluate the level of miR-130b and miR-218 expressions in OS patients and normal tissues and their relationship with clinicopathological features and survival in OS patients.

resultsQRT-PCR indicated that miR-130b expression in tumor tissues was strongly elevated than adjacent non-tumor tissues (P < 0.001), while the level of miR-218 expression in osteosarcoma tissues was down-regulated than adjacent non-tumor tissues (P < 0.001). We evaluated the clinical significance of miR-130b and miR-218 in osteosarcoma. Clinical correlation analysis showed that increased expression of miR-130b and decreased expression of miR-218 were significantly associated with advanced tumor stage (x (2) = 6.285, P < 0.009; x (2) = 7.172, P < 0.007), distant metastasis (x (2)  = 5.528; P < 0.001; x (2) = 4.617, P < 0.001) and size of tumor (x (2) = 5.01, P = 0.013; x (2) = 4.271, P = 0.019).

conclusionsTaken together, our data indicated that high miR-130b level and low level of miR-218 are associated with poor clinicopathological characteristics. Furthermore, miR-130b may play a key role in the progression of osteosarcoma.

Indexed as

Real-Time Polymerase Chain ReactionAdultBiomarkers, TumorBiopsyBone NeoplasmsChi-Square DistributionDown-RegulationEarly Detection of CancerFemaleGene Expression Regulation, NeoplasticHumansMaleMicroRNAsNeoplasm StagingOsteosarcomaPredictive Value of TestsBiomarkers, TumorMicroRNAsMIRN130 microRNA, humanMIRN218 microRNA, human

Identifiers

PMID26446495
PMCPMC4596511

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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.