Evidence map›Paper›PMID 34196116›Full record

ArticleCancer medicine2021

A prognostic nomogram based on competing endogenous RNA network for clear-cell renal cell carcinoma.

Yun Peng, Shangrong Wu, Zihan Xu, Dingkun Hou, Nan Li, Zheyu Zhang, Lili Wang, Haitao Wang

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 55% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Machine Learning Gene Signature to Metastatic ccRCC Based on ceRNA Network.International journal of molecular sciences · 2024
    Article
  2. Article
  3. 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

8 authors at 1 institution in 1 country.

Yun PengTianjin Institute of Urology, The 2nd Hospital of Tianjin Medical University, Tianjin, China.
Shangrong WuTianjin Institute of Urology, The 2nd Hospital of Tianjin Medical University, Tianjin, China.
Zihan XuTianjin Institute of Urology, The 2nd Hospital of Tianjin Medical University, Tianjin, China.
Dingkun HouTianjin Institute of Urology, The 2nd Hospital of Tianjin Medical University, Tianjin, China.
Nan LiTianjin Institute of Urology, The 2nd Hospital of Tianjin Medical University, Tianjin, China.
Zheyu ZhangTianjin Institute of Urology, The 2nd Hospital of Tianjin Medical University, Tianjin, China.
Lili WangDepartment of Oncology, Tianjin Medical University Second Hospital, Hexi, Tianjin, China.
Haitao WangDepartment of Oncology, Tianjin Medical University Second Hospital, Hexi, Tianjin, China.ORCID 0000-0003-4345-9375
Second Hospital of Tianjin Medical University · CN

Funding

National Natural Science Foundation of China 81572543Science and Technology Support Program of Tianjin 17ZXMFSY00040
6 · The paper itself

Abstract

backgroundClear-cell renal cell carcinoma (ccRCC) is stubborn to traditional chemotherapy and radiation treatment, which makes its clinical management a major challenge. Recently, we have made efforts in understanding the etiology of ccRCC. Increasing evidence revealed that the competing endogenous RNA (ceRNA) was involved in the development of varied tumors. However, a comprehensive analysis of the prognostic model based on lncRNA-miRNA-mRNA ceRNA regulatory network of ccRCC with large-scale sample size and RNA-sequencing expression data is still limited.

methodsRNA-sequencing expression data were taken out from GTEx database and TCGA database, a total of 354 samples with ccRCC and 157 normal controlled samples were included in our study. The ccRCC-specific genes were obtained by WGCNA and differential expression analysis. Following, the communication of mRNAs and lncRNAs with targeted miRNAs were predicted by MiRcode, starBase, miRTarBase, and TargetScan. A gene signature of eight genes was further constructed by univariate Cox regression, Lasso methods, and multivariate Cox regression analysis.

resultsA total of 2191 mRNAs and 1377 lncRNAs was identified, and a dysregulated ceRNA network for ccRCC was established using 7 mRNAs, 363 lncRNAs, and 3 miRNAs. Further, a gene signature including eight genes based on this ceRNA was determined followed by the development of a nomogram predicting 1-, 3-, and 5-year survival probability for ccRCC.

conclusionIt could contribute to a better understanding of ccRCC tumorigenesis mechanism and guide clinicians to make a more accurate treatment decision.

Indexed as

Gene Regulatory NetworksNomogramsBiomarkers, TumorCarcinogenesisCarcinoma, Renal CellDatasets as TopicGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateKidney NeoplasmsMicroRNAsRisk AssessmentRNA, Long NoncodingRNA, MessengerRNA-SeqBiomarkers, TumorMicroRNAsRNA, Long NoncodingRNA, Messengercompeting endogenous RNAgene signaturenomogramsrenal cell carcinoma

Identifiers

PMID34196116
PMCPMC8366097
OpenAlexW3115305875

What OpenQuestion holds

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LicenceCC BY
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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.