Evidence map›Paper›PMID 38022698›Full record

ArticleComputational and structural biotechnology journal2023

Identification of a 24-gene panel and a novel marker of

Xiaoshi Ma, Lipeng Chen, Tao Chen, Kun Chen, Huirong Zhang, Kaipeng Huang, Han Zheng, Hongtao Jin, Zhiqiang Cheng, Kefeng Xiao and 1 more

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
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  4. Review
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.

Xiaoshi MaDepartment of Urology, Shenzhen People's Hospital (The Second Clinical Medical College of Jinan University), Shenzhen 518020, Guangdong, China.
Lipeng ChenClinical Medical Research Center, Shenzhen People's Hospital (The Second Clinical Medical College of Jinan University), Shenzhen 518020, Guangdong, China.
Tao ChenSchool of Medicine, Southern University of Science and Technology, Shenzhen 518055, Guangdong, China.
Kun ChenDepartment of Radiotherapy, Nanjing Medical University The Fourth School of Clinical Medicine, Nanjing 210000, Jiangsu, China.
Huirong ZhangClinical Medical Research Center, Shenzhen People's Hospital (The Second Clinical Medical College of Jinan University), Shenzhen 518020, Guangdong, China.
Kaipeng HuangDepartment of Pathology, Shenzhen People's Hospital (The Second Clinical Medical College of Jinan University), Shenzhen 518020, Guangdong, China.
Han ZhengDepartment of Urology, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu 241000, Anhui, China.
Hongtao JinDepartment of Radiotherapy, Nanjing Medical University The Fourth School of Clinical Medicine, Nanjing 210000, Jiangsu, China.
Zhiqiang ChengDepartment of Pathology, Third People's Hospital of Shenzhen (The Second Affiliated Hospital of Southern University of Science and Technology), Shenzhen 518100, Guangdong, China.
Kefeng XiaoDepartment of Urology, Shenzhen People's Hospital (The Second Clinical Medical College of Jinan University), Shenzhen 518020, Guangdong, China.
Jinan GuoDepartment of Urology, Shenzhen People's Hospital (The Second Clinical Medical College of Jinan University), Shenzhen 518020, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise diagnosis of early prostate cancer (PCa) is critical for preventing tumor progression. However, the diagnostic outcomes of currently used markers are far from satisfactory due to the low sensitivity or specificity. Here, we identified a diagnostic subpopulation in PCa tissue with the integrating analysis of single-cell and bulk RNA-seq. The representative markers of this subpopulation were extracted to perform intersection analysis with early-PCa-related gene module generated from weighted correlation network analysis (WGCNA). A total of 24 overlapping genes were obtained, the diagnostic roles of which were validated by distinguishing normal and tumorous prostate samples from the public dataset. A least absolute shrinkage and selection operator (LASSO) model was constructed based on these genes and the obtained 24-gene panel showed high sensitivity and specificity for PCa diagnosis, with better identifying capability of PCa than the commercially used gene panel of Oncotype DX. The top two risk factors,

Indexed as

24-gene panelEarly diagnosisPODXL2Prostate cancerSingle-cell and bulk RNA-seqTRPM4

Identifiers

PMID38022698
PMCPMC10663703

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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.