Evidence map›Paper›PMID 35836879›Full record

ArticleAmerican journal of translational research2022

A systematic pan-cancer analysis identifies RIOK3 as an immunological and prognostic biomarker.

Jian Li, Ruili Sun, Lixiang He, Guoyi Sui, Wenyu Di, Jian Yu, Wei Su, Zenggang Pan, Yu Zhang, Jinghang Zhang and 1 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

11 authors at 3 institutions in 2 countries.

Jian LiDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Ruili SunHenan Key Laboratory of Immunology and Targeted Drugs, School of Laboratory Medicine, Xinxiang Medical University Xinxiang 453003, Henan, China.
Lixiang HeDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Guoyi SuiDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Wenyu DiDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Jian YuDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Wei SuDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Zenggang PanDepartment of Pathology, Yale University School of Medicine New Haven, CT 06520, US.
Yu ZhangSchool of Basic Medical Sciences, Xinxiang Medical University Xinxiang 453003, Henan, China.
Jinghang ZhangDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Feng RenDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University Xinxiang 453003, Henan, China.
Xinxiang Medical University · CNHenan Normal University · CNYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDespite recent research highlighting the critical function of RIO kinase 3 (RIOK3) in a variety of malignancies, a comprehensive evaluation of RIOK3 in human tumors is absent. Our study helps to clarify the molecular mechanism of RIOK3 in carcinogenesis from multiple perspectives.

methodsOur research looked into the potential oncogenic role of RIOK3 in 33 cancers using TCGA (The Cancer Genome Atlas), GTEx (Genotype-Tissue Expression Project), GEO (Gene Expression Omnibus) datasets, and several bioinformatics tools.

resultsRIOK3 expression in tumors is disordered compared to normal tissue, and it is highly linked with the level of MMR (Mismatch repair) gene mutations and DNA methyltransferase expression. According to univariate survival analysis, it could be used as an independent prognostic factor. Further investigation demonstrated that RIOK3 expression was correlated with cancer-associated fibroblast, neutrophil, and endothelial infiltration levels in kidney cancer and was positively correlated with the expression of immune checkpoint markers in different cancers. The functional pathways of RIOK3 also included cell-cell adhesion, protein phosphorylation, and innate immune-related functions.

conclusionsThese findings suggest that RIOK3 could be used as an immunological and prognostic biomarker in various malignant tumors.

Indexed as

immune infiltrationmethylationpan-cancerprognosisRIOK 3

Identifiers

PMID35836879
PMCPMC9274588
OpenAlexW4285614720

What OpenQuestion holds

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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.