Evidence map›Paper›PMID 34760693›Full record

ArticleFrontiers in oncology2021

Risk Scores Based on Six Survival-Related RNAs in a Competing Endogenous Network Composed of Differentially Expressed RNAs Between Clear Cell Renal Cell Carcinoma Patients Carrying Wild-Type or Mutant Von Hippel-Lindau Serve Well to Predict Malignancy and Prognosis.

Rui Zhu, Xiezhao Li, Zhiduan Cai, Siyang Liang, Yaoji Yuan, Yuyu Xu, Dehui Lai, Haibo Zhao, Weiqing Yang, Jun Bian and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 61% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 1 institution in 1 country.

Rui ZhuDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Xiezhao LiDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Zhiduan CaiDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Siyang LiangDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Yaoji YuanDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Yuyu XuDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Dehui LaiDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Haibo ZhaoDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Weiqing YangDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Jun BianDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Leyuan LiuDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Guibin XuDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) carrying wild-type Von Hippel-Lindau (VHL) tumor suppressor are more invasive and of high morbidity. Concurrently, competing endogenous RNA (ceRNA) network has been suggested to play an important role in ccRCC malignancy. In order to understand why the patients carrying wild-type VHL gene have high degrees of invasion and morbidity, we applied bioinformatics approaches to identify 861 differentially expressed RNAs (DE-RNAs) between patients carrying wild-type and patients carrying mutant VHL from The Cancer Genome Atlas (TCGA) database, established a ceRNA network including 122 RNAs, and elected six survival-related DE-RNAs including Linc00942, Linc00858, RP13_392I16.1, hsa-miR-182-5p, hsa-miR-183-5p, and PAX3. Examining clinical samples from our hospital revealed that patients carrying wild-type VHL had significantly higher levels of all six RNAs than those carrying mutant VHL. Patients carrying wild-type VHL had significantly higher risk scores, which were calculated based on expression levels of all six RNAs, than those carrying mutant VHL. Patients with higher risk scores had significantly shorter survival times than those with lower risk scores. Therefore, the risk scores serve well to predict malignancy and prognosis.

Indexed as

ccRCCceRNA networkprognosisrisk scoreVHL

Identifiers

PMID34760693
PMCPMC8573174
OpenAlexW3211171027

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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.