Evidence map›Paper›PMID 35297481›Full record

ArticleBioscience reports2022

Overexpression of prothymosin-α in glioma is associated with tumor aggressiveness and poor prognosis.

Anurag Kumar, Vikas Kumar, Mohit Arora, Manish Kumar, Prajwal Ammalli, Bhaskar Thakur, Jitender Prasad, Sarita Kumari, Mehar Chand Sharma, Shashank Sharad Kale and 1 more

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2022. 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, 11 citations in OpenAlex.

  1. Article
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  6. Wogonin inhibits hepatoma cell proliferation by targeting miR-27b-5p/YWHAZ axis.Journal of biochemical and molecular toxicology · 2023
    Article
  7. TargetedCell reports methods · 2023
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  8. 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

11 authors at 4 institutions in 1 country.

Anurag Kumar *Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-5283-1821
Vikas Kumar *Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-4291-7787
Mohit AroraDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-7417-5036
Manish KumarDepartment of Biochemistry, All India Institute of Medical Sciences, Bilaspur, India.
Prajwal AmmalliDepartment of Biochemistry, National Institute of Mental Health and Neuro-Sciences, Bengaluru, India.
Bhaskar ThakurDivision of Biostatistics, Kalinga Institute of Medical Sciences, KIIT University, Bhubaneswar, India.
Jitender PrasadDepartment of Biochemistry, All India Institute of Medical Sciences, Deoghar, India.
Sarita KumariLab Oncology Unit, Dr. B.R.A-IRCH, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-9566-2933
Mehar Chand SharmaDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Shashank Sharad KaleDepartment of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.
Shyam S ChauhanDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-4796-5171
All India Institute of Medical Sciences · INAll India Institute of Medical Sciences, Deoghar · INInstitute of Medical Sciences · INNational Institute of Mental Health and Neurosciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prothymosin-α (PTMA), a nuclear protein, is strikingly associated with unfavorable clinical outcomes in many cancers. However, no information about its clinical relevance in glioma was available. Therefore in the present study, we evaluated the prognostic utility of this protein in a cohort of 81 glioma patients. The PTMA expression was assessed by immunohistochemical analysis, quantitative PCR, and Western blotting. Furthermore, the association of PTMA with clinicopathological features and molecular alterations were assessed in the patient cohort and validated in multiomics datasets, The Cancer Genome Atlas (TCGA; n=667) and Chinese Glioma Genome Atlas (CGGA; n=1013). We observed an increase in PTMA expression with increasing histological grades of this malignancy. PTMA immunostaining also displayed a strong positive association with the MIB-1 index. Univariate analysis revealed a superior prognostic value of PTMA to predict overall survival (OS) as compared with the routinely used markers (p53, isocitrate dehydrogenase (IDH) 1 (IDH1), α-thalassemia/intellectual disability syndrome X-linked (ATRX), and Ki-67). Interestingly, in Cox regression analysis it emerged as an independent predictor of OS (hazard ratio (HR) = 13.71, 95% CI = 5.96-31.52, P<0.0001). Thus, our results demonstrate the potential prognostic utility of PTMA in glioma which may prove useful in the management of this deadly malignancy.

Indexed as

Brain NeoplasmsGliomaBiomarkers, TumorCohort StudiesHumansProportional Hazards ModelsBiomarkers, TumorGBMPrognosisPTMASurvival

Identifiers

PMID35297481
PMCPMC9069441
OpenAlexW4220713534

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Registered trials

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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.