Evidence map›Paper›PMID 34231338›Full record

ArticleFEBS open bio2021

Overexpression of HPRT1 is associated with poor prognosis in head and neck squamous cell carcinoma.

Mohsen Ahmadi, Maryam Eftekhari Kenzerki, Seyed Mohammad Akrami, Salar Pashangzadeh, Fatemeh Hajiesmaeili, Sahereh Rahnavard, Leila Habibipour, Negin Saffarzadeh, Pegah Mousavi

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 28 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

9 authors at 4 institutions in 1 country.

Mohsen AhmadiStudent Research Committee, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.ORCID 0000-0003-4751-4212
Maryam Eftekhari KenzerkiStudent Research Committee, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Seyed Mohammad AkramiDepartment of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Iran.
Salar PashangzadehIranian Research Center for HIV/AIDS, Iranian Institute for Reduction of High-Risk Behaviors, Tehran University of Medical Sciences, Iran.
Fatemeh HajiesmaeiliDivision of Medical Genetics, Booali Medical Diagnostic Laboratory, Qom, Iran.
Sahereh RahnavardDepartment of Cellular and Molecular Biology, Ahar Branch, Islamic Azad University, Ahar, Iran.
Leila HabibipourMolecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Negin SaffarzadehDepartment of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Iran.
Pegah MousaviDepartment of Medical Genetics, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Hormozgan University of Medical Sciences · IRIran University of Medical Sciences · IRIranian Institute for Health Sciences Research · IRIslamic Azad University of Ahar · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxanthine phosphoribosyltransferase (HPRT1), as a salvage pathway enzyme, plays a crucial role in modulating the cell cycle and has been reported to be overexpressed in multiple cancers. Nevertheless, the relationship between the HPRT1 gene and head and neck squamous cell carcinomas (HNSCCs) has not been investigated so far. In this study, we first evaluated the expression and clinical value of HPRT1 mRNA and protein in tumor and healthy control tissues. Then, we examined mutations of the HPRT1 gene and their association with survival outcomes of patients with HNSCC. We also performed functional analyses of HPRT1 coexpressed genes and examined the association between HPRT1 expression and drug sensitivity. Both HPRT1 mRNA and protein were significantly higher in HNSCC compared with normal tissues, and up-regulation of HPRT1 was also correlated with age, sex, pathological stage and histological grades of patients with HNSCC. Moreover, HPRT1 and its associated genes were observed to be enriched for several cancer-related pathways, including DNA replication and cell cycle. Finally, patients exhibiting overexpression of the HPRT1 gene may be resistant to abiraterone and sensitive to several drugs, including tozasertib and teniposide. This study demonstrated that the elevated expression of HPRT1 gene is correlated with the progression of HNSCC; thus, this gene may serve as a useful indicator for the early detection, risk stratification and targeted therapy of patients with HNSCC.

Indexed as

Biomarkers, TumorGene ExpressionComputational BiologyDatabases, GeneticDNA Mutational AnalysisDrug Resistance, NeoplasmGene Expression ProfilingGene Expression Regulation, NeoplasticHumansHypoxanthine PhosphoribosyltransferaseMutationRNA, MessengerROC CurveSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorHypoxanthine PhosphoribosyltransferaseRNA, MessengerbioinformaticsbiomarkerGEOhead and neck cancerHPRT1TCGA

Identifiers

PMID34231338
PMCPMC8409317
OpenAlexW3177942712

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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.