Evidence map›Paper›PMID 34121368›Full record

ArticleCancer medicine2021

Integrative analysis of TP73 profile prognostic significance in WHO grade II/III glioma.

Yanming Chen, Ye Wang, Qiheng He, Wen Wang, Tan Zhang, Zhongyong Wang, Jun Dong, Qing Lan, Jizong Zhao

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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  6. Case Report: A novelFrontiers in oncology · 2022
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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 2 institutions in 1 country.

Yanming ChenDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.ORCID 0000-0001-9194-0580
Ye WangHeath Management Center, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Qiheng HeDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Wen WangChina National Clinical Research Center for Neurological Diseases, Beijing, China.
Tan ZhangDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Zhongyong WangDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Jun DongDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Qing LanDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Jizong ZhaoDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Soochow University · CNCapital Medical University · CN

Funding

National Natural Science Foundation of China 81620183the Youth Medical Talent Foundation of Jiangsu QNRC2016870
6 · The paper itself

Abstract

Due to the extremely intrinsic heterogeneity among glioma patients, the outcomes of these patients are tremendously different. Therefore, the exploitation of novel biomarker classification of glioma is vitally important for deep insight into the essence and predicting the prognosis of glioma. We aim to analyze the correlation between TP73 mRNA expression, DNA methylated alteration and the prognosis of WHO grade II/III glioma, utilizing bioinformatics to evaluate its significance as a risk-factor in predicting the prognosis of these glioma patients. The analysis found that TP73 expression was positively correlated with the grade of glioma, and showed a strong correlation with glioma molecular classification, which revealed significantly higher TP73 expression in IDH-wildtype than in IDH-mutant subtype of WHO grade II/III glioma. Cox regression analysis indicated that high expression of TP73 shared an independent high-risk factor impacting the prognosis of WHO grade II/III glioma. We discovered 8 DNA promoter methylation sites with prognostic significance, which were negatively associated with TP73 expression, and positively associated with beneficial overall survival (OS) and progression-free survival (PFS). Integrating with four independent glioma datasets, subsequent Meta-analysis verified that low expression of TP73 was closely related to favorable OS, especially in IDH-mutant subtype. Moreover, we found that 1p/19q

Indexed as

MutationAgedBrain NeoplasmsChromosomes, Human, Pair 1DNA MethylationFemaleGene ExpressionGenetic MarkersGliomaHumansMaleMiddle AgedNeoplasm GradingPrognosisProgression-Free SurvivalPromoter Regions, GeneticGenetic MarkersRNA, MessengerTP73 protein, humanTumor Protein p73biomarkerscancers risk factorsmethylationprognosissurvival

Identifiers

PMID34121368
PMCPMC8267133
OpenAlexW3171112014

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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.