Evidence map›Paper›PMID 33643601›Full record

ArticleTherapeutic advances in chronic disease2021

Identification of mortality-risk-related missense variant for renal clear cell carcinoma using deep learning.

Jin-Bor Chen, Huai-Shuo Yang, Sin-Hua Moi, Li-Yeh Chuang, Cheng-Hong Yang

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in chronic disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

5 authors at 4 institutions in 2 countries.

Jin-Bor ChenDivision of Nephrology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung.
Huai-Shuo YangDepartment of Electronic Engineering, National Kaohsiung University of Applied Sciences, Kaohsiung.
Sin-Hua MoiDepartment of Chemical Engineering and Institute of Biotechnology and Chemical Engineering, I-Shou University, Kaohsiung.
Li-Yeh ChuangDepartment of Chemical Engineering and Institute of Biotechnology and Chemical Engineering, I-Shou University, Kaohsiung.
Cheng-Hong YangDepartment of Electronic Engineering, National Kaohsiung University of Applied Sciences, Kaohsiung, 415 Jiangong Road, San-Min District, Kaohsiung, 82444.ORCID https://orcid.org/0000-0002-2741-0072
Czech Academy of Sciences, Institute of Biotechnology · CZChang Gung University · TWKaohsiung Medical University · TWNational Kaohsiung University of Applied Sciences · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionKidney renal clear cell carcinoma (KIRCC) is a highly heterogeneous and lethal cancer that can arise in patients with renal disease. DeepSurv combines a deep feed-forward neural network with a Cox proportional hazards function and could provide optimized survival results compared with convenient survival analysis.

methodsThis study used an improved DeepSurv algorithm to identify the candidate genes to be targeted for treatment on the basis of the overall mortality status of KIRCC subjects. All the somatic mutation missense variants of KIRCC subjects were abstracted from TCGA-KIRC database.

resultsThe improved DeepSurv model (95.1%) achieved greater balanced accuracy compared with the DeepSurv model (75%), and identified 610 high-risk variants associated with overall mortality. The results of gene differential expression analysis also indicated nine KIRCC mortality-risk-related pathways, namely the tRNA charging pathway, the D-myo-inositol-5-phosphate metabolism pathway, the DNA double-strand break repair by nonhomologous end-joining pathway, the superpathway of inositol phosphate compounds, the 3-phosphoinositide degradation pathway, the production of nitric oxide and reactive oxygen species in macrophages pathway, the synaptic long-term depression pathway, the sperm motility pathway, and the role of

conclusionThe results proved that the improved DeepSurv model effectively classified mortality-related high-risk variants and identified the candidate genes. In the context of KIRCC overall mortality, the proposed model effectively recognized mortality-related high-risk variants for KIRCC.

Indexed as

deep learningKidney renal clear cell carcinomasurvival analysis

Identifiers

PMID33643601
PMCPMC7890720
OpenAlexW3131147288

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.