Evidence map›Paper›PMID 37340189›Full record

ArticleJournal of cancer research and clinical oncology2023

Integrated analysis of the roles of oxidative stress related genes and prognostic value in clear cell renal cell carcinoma.

Danwen Wang, Zhao Deng, Mengxin Lu, Kai Deng, Zhiqiang Li, Fenfang Zhou

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. [Research Progress on the Role and Mechanisms of PYCR1 
in Tumorigenesis and Progression].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. The Role of Redox Environment in Tumors.Current medicinal chemistry · 2025
    Review
  9. Article
  10. 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

6 authors at 2 institutions in 1 country.

Danwen Wang *Department of Neurosurgery, Zhongnan Hospital, Wuhan University, Wuhan, China.
Zhao Deng *Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Mengxin LuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Kai DengDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Zhiqiang LiDepartment of Neurosurgery, Zhongnan Hospital, Wuhan University, Wuhan, China. lizhiqiang@whu.edu.cn.
Fenfang Zhou *Department of Radiology, Zhongnan Hospital of Wuhan University, Wuhan, China. zhoufenfang@whu.edu.cn.
Wuhan University · CNZhongnan Hospital of Wuhan University · CN

Funding

Natural Science Foundation of Hubei Province 2021CFB055the program of Excellent Doctoral (Postdoctoral) of Zhongnan Hospital of Wuhan University No. ZNYB2019006 and ZNYB2021022
6 · The paper itself

Abstract

backgroundPatients with clear cell renal cell carcinoma (ccRCC), which is the most commonly diagnosed subtype of renal cell carcinoma, are at risk of tumor metastasis and recrudescence. Previous research has shown that oxidative stress can induce tumorigenesis in many cancers and can be a target of cancer treatment. Despite these findings, little progress has been made understanding in the association of oxidative stress-related genes (OSRGs) with ccRCC.

methodsIn vitro experiments were conducted with MTT survival assays, qRT‒PCR, apoptosis assays, cell cycle assays, ROS assays, and IHC staining.

resultsIn our study, 12 differentially expressed oxidative stress-related genes (DEOSGs) and related transcription factors (TFs) that are relevant to overall survival (OS) were screened, and their mutual regulatory networks were constructed with data from the TCGA database. Moreover, we constructed a risk model of these OSRGs and performed clinical prognostic analysis and validation. Next, we performed protein-protein interaction (PPI) network analysis and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis of MELK, PYCR1, and PML. A tissue microarray also verified the high expression of MELK and PYCR1 in ccRCC. Finally, in vitro cellular experiments demonstrated that knockdown of MELK or PYCR1 significantly inhibited ccRCC cell proliferation by causing cell apoptosis and inducing cell cycle arrest in the G1 phase. Intracellular ROS levels were elevated after these two genes were knocked down.

conclusionOur results revealed the potential DEORGs to be used in ccRCC prognostic prediction and identified two biomarkers, named PYCR1 and MELK, which regulated the proliferation of ccRCC cells by affecting ROS levels. Furthermore, PYCR1 and MELK could be promising targets for predicting the progression and prognosis of ccRCC, thereby serving as new targets for medical treatments.

Indexed as

CarcinomaCarcinoma, Renal CellKidney NeoplasmsHumansNeoplasm Recurrence, LocalPrognosisProtein Serine-Threonine KinasesReactive Oxygen SpeciesMELK protein, humanProtein Serine-Threonine KinasesReactive Oxygen SpeciesccRCCMELKOSRGsPYCR1ROS

Identifiers

PMID37340189
PMCPMC10465389
OpenAlexW4381434106

What OpenQuestion holds

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LicenceCC BY
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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.