Evidence map›Paper›PMID 33447054›Full record

ArticleOncoTargets and therapy2021

PDIA4 Correlates with Poor Prognosis and is a Potential Biomarker in Glioma.

Haoyu Li, Qing Liu, Kai Xiao, Zhengxi He, Chao Wu, Jianjun Sun, Xin Chen, Suhua Chen, Jun Yang, Qianquan Ma and 1 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  9. A Novel HOXA10-Associated 5-Gene-Based Prognostic Signature for Stratification of Short-term Survivors of Pancreatic Ductal Adenocarcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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 5 institutions in 1 country.

Haoyu LiDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan, People's Republic of China.
Qing LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan, People's Republic of China.
Kai XiaoDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan, People's Republic of China.
Zhengxi HeDepartment of Oncology, Xiangya Hospital, Central South University, Changsha 410008, Hunan, People's Republic of China.
Chao WuDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing 100191, People's Republic of China.
Jianjun SunDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing 100191, People's Republic of China.
Xin ChenDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing 100191, People's Republic of China.
Suhua ChenDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing 100191, People's Republic of China.
Jun YangDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing 100191, People's Republic of China.
Qianquan MaDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing 100191, People's Republic of China.
Jun SuDepartment of Neurosurgery, Hunan Children's Hospital, Changsha 410007, Hunan, People's Republic of China.
Peking University · CNPeking University Third Hospital · CNCentral South University · CNXiangya Hospital Central South University · CNHunan Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGliomas, characterized by aggressiveness and invasiveness, remain incurable after conventional therapies. The molecular mechanisms driving the progression and maintenance of glioma are still poorly understood.

methodsThe TCGA and CGGA databases were chosen for bioinformatics analysis. Gene expression profiling interactive analysis (GEPIA) was performed for differential analysis. The Kaplan-Meier method was chosen for survival analysis. Analysis of stromal and immune infiltration was performed using the ESTIMATE algorithm and xCell package. qPCR and Western blotting were performed to measure the expression of PDIA4 at the mRNA and protein levels. IHC was performed to detect the expression of PDIA4 in glioma tissues. The viability of glioma cells was evaluated by the CCK8 assay.

resultsIn this study, we identified high PDIA4 expression in gliomas that correlated with poor prognosis. The association between IDH1 and different glioma patterns also indicated the potential biological role of PDIA4 in tumor development. Mechanistically, PDIA4 interacted with multiple immunological components to promote an immunosuppressive tumor microenvironment (TME). Knockdown of PDIA4 significantly impaired the proliferation of GBM cells.

conclusionOur results confirm that PDIA4 is an efficient biomarker of gliomas, with clinical implications for prognosis and therapeutic strategies.

Indexed as

biomarkergliomaimmune cellsPDIA4prognosis

Identifiers

PMID33447054
PMCPMC7802790
OpenAlexW3120062946

What OpenQuestion holds

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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.