Evidence map›Paper›PMID 35273703›Full record

ArticleAmerican journal of translational research2022

Gene expression based profiling of pleomorphic xanthoastrocytoma highlights two prognostic subgroups.

Jyotsna Singh, Iman Dandapath, Prerana Jha, Nidhi Shukla, Rahul Gupta, Amit Katiyar, Vikas Sharma, Swati Mahajan, Sujata Chaturvedi, Arvind Ahuja and 9 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. PXA-like tumors: prognostic implications.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    Article
  2. 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

19 authors at 1 institution in 1 country.

Jyotsna SinghDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Iman DandapathDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Prerana JhaDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Nidhi ShuklaDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Rahul GuptaDepartment of Biochemical Engineering and Biotechnology, Indian Institute of Technology Delhi New Delhi, India.
Amit KatiyarCCRF, All India Institute of Medical Sciences New Delhi, India.
Vikas SharmaCCRF, All India Institute of Medical Sciences New Delhi, India.
Swati MahajanDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Sujata ChaturvediDepartment of Pathology, Institute of Human Behaviour and Allied Sciences New Delhi, India.
Arvind AhujaDepartment of Pathology, PGIMER & Dr. RML Hospital New Delhi, India.
Meenakshi BhardwajDepartment of Pathology, PGIMER & Dr. RML Hospital New Delhi, India.
Ravindra SaranDepartment of Pathology, GB Pant Institute of Postgraduate Medical Education and Research New Delhi, India.
Ajay GargDepartment of Neuroradiology, All India Institute of Medical Sciences New Delhi, India.
Mehar C SharmaDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Niveditha ManjunathDepartment of Neurosurgery, All India Institute of Medical Sciences New Delhi, India.
Ashish SuriDepartment of Neurosurgery, All India Institute of Medical Sciences New Delhi, India.
Ritu KulshreshthaDepartment of Biochemical Engineering and Biotechnology, Indian Institute of Technology Delhi New Delhi, India.
Chitra SarkarDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
Vaishali SuriDepartment of Pathology, All India Institute of Medical Sciences New Delhi, India.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPleomorphic xanthoastrocytomas (PXAs) are rare, accounting for less than 1% of astrocytomas, and commonly occur in young patients. The majority are WHO grade II. A fraction of tumors that present or recur with malignant change are classified as anaplastic (APXA, grade III). Limited data are available on their molecular characteristics. METHODOLOGY: Genome-wide expression profiling of 14 PXA and 6 APXAs was performed by microarray. Among differentially expressed genes (DEGs), Cyclin-Dependent Kinase 14 (

resultUnsupervised hierarchical clustering revealed two distinct molecular clusters (Cluster 1: 10 PXA, 3 APXA and Cluster 2: 4 PXA, 3 APXA) with grade II and III tumors distributed in both highlighting molecular heterogeneity within the same grade. There was an insignificant difference in age, sex, immunohistochemical profile, frequency of

conclusionThis is the first comprehensive study highlighting distinct molecular subgroups of PXA. The differentially expressed genes between two clusters may potentially be used for developing histology independent classification schemes, prognostication and may serve as prospective therapeutic targets for PXA patients.

Indexed as

BRAFCDK14CDKN2AExpression profilingmolecular clustersMTFP1PXA/APXAunsupervised hierarchical clustering

Identifiers

PMID35273703
PMCPMC8902531
OpenAlexW4225363090

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.