Evidence map›Paper›PMID 35414328›Full record

ArticleCell cycle (Georgetown, Tex.)2022

Expression status and prognostic value of autophagy-related lncRNAs in prostate cancer.

Guo Chen, Xiaoping Qin, Yu Wang, Biyun Gao, Muan Ling, Wenjun Yin, Yutong Li, Bin Pan

Open access · greenAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2022. 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
0.7field-weighted citation impact, top 37% 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, 7 citations in OpenAlex.

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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.

Guo ChenDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Xiaoping QinDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Yu WangDepartment of Endocrinology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Biyun GaoDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Muan LingDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Wenjun YinDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Yutong LiDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Bin PanDepartment of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
First Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNAs involve in the autophagy to regulate prostate cancer (PCA) initiation and progression. Therefore, it urges to explore more significant AR-lncRNAs in PCa. mRNA data and clinical information of PCa were achieved from TCGA database, and ARGs were obtained from the HADb. AR-lncRNAs were identified by correlation analysis of DE ARGs and lncRNAs. Univariate Cox regression, LASSO regression, and multivariate Cox regression were used to identify the prognostic AR-lncRNA signature and constructed a risk model. GESA was used to biological function analysis between high- and low-risk score group. A nomogram was constructed and used to predicate the survival of PCa patients. A calibration curve was used to determine the accuracy of the predication model. AR-related ceRNA network was constructed by correlation analysis. Expression of six AR-related lncRNAs were detected by qRT-PCR. 222 ARGs and 385 AR-lncRNAs were screened from PCa and normal tissues, and 17 AR-lncRNAs were identified as prognostic signature for PCa. Based on the expression of prognostic signature, a risk score was calculated, and PCa samples were distributed into high- and low-risk score groups. The biological function and predicated value of the prognostic signature were also examined. Finally, based on the correlation between each ARG and its prognostic signature, three modules of AR-lncRNA-miRNA-mRNA regulatory networks were constructed based on 6 AR-lncRNAs, 17 miRNAs, and 12 ARGs. And we found that AC012085.2, UBXN10-AS1, LINC00261 downregulated, whereas AP004608.1, AC104667.2, AC008610.1 upregulated in PCa compared with BPH tissues. Our finding supplied the potential AR-lncRNAs prognostic signature for PCa.

Indexed as

MicroRNAsProstatic NeoplasmsRNA, Long NoncodingAutophagyBiomarkers, TumorGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMalePrognosisRNA, MessengerBiomarkers, TumorMicroRNAsRNA, Long NoncodingRNA, Messengerautophagy-related long non-coding RNAscompeting endogenous RNA networkprognosisProstate cancer

Identifiers

PMID35414328
PMCPMC9302510
OpenAlexW4223427466

What OpenQuestion holds

Textmetadata
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.