Evidence map›Paper›PMID 36186485›Full record

ArticleFrontiers in genetics2022

Development and validation of a TRP-related gene signature for overall survival prediction in lung adenocarcinoma.

Min He, Gujie Wu, Ziheng Wang, Kuan Ren, Zheng Yang, Qun Xue

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Min HeMedical College of Nantong University, Nantong, Jiangsu, China.
Gujie WuMedical College of Nantong University, Nantong, Jiangsu, China.
Ziheng WangResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Kuan RenMedical College of Nantong University, Nantong, Jiangsu, China.
Zheng YangCardiothoracic Surgery Department, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Qun XueResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transient receptor potential (TRP) channel is a type of channel protein widely distributed in peripheral and central nervous systems. Genes encoding TRP can be regulated by natural aromatic substances and serve as a therapeutic target for many diseases. However, the role of TRP-related genes in lung adenocarcinoma (LUAD) remains unclear. In this study, we used data from TCGA to screen and identify 17 TRP-related genes that are differentially expressed between LUAD and normal lung tissues. Based on these differentially expressed genes (DEGs), we classified all patients with LUAD into two subtypes. Significant differences in prognosis, clinical features, and immune cell infiltration characteristics were observed between the two subtypes. Subsequently, a prognostic signature with 12 genes was established by applying the least absolute shrinkage and selection operator (LASSO) Cox regression method, and all patients with LUAD were classified into low- and high-risk groups. Patients with LUAD in the low-risk group had a significantly longer survival time than those in the high-risk group (

Indexed as

gene signatureimmunelung adenocarcinomaprognosisTRP-related gene

Identifiers

PMID36186485
PMCPMC9521679

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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.