Evidence map›Paper›PMID 37427142›Full record

ArticleFrontiers in oncology2023

Integrated analysis of single-cell and Bulk RNA sequencing reveals a malignancy-related signature in lung adenocarcinoma.

Mengxi Wu, Zhenyu Wu, Jun Yan, Jie Zeng, Jun Kuang, Chenghua Zhong, Xiaojia Zhu, Yijun Mo, Quanwei Guo, Dongfang Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

13 authors at 3 institutions in 1 country.

Mengxi WuDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Zhenyu WuDepartment of Urology, The First People's Hospital of Foshan, Foshan, China.
Jun YanDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jie ZengDepartment of Thoracic Surgery, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, China.
Jun KuangDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Chenghua ZhongDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Xiaojia ZhuDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Yijun MoDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Quanwei GuoDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Dongfang LiDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jianfeng TanDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Tao ZhangDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jianhua ZhangDepartment of Thoracic Surgery, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Southern Medical University Shenzhen Hospital · CNFirst People's Hospital of Foshan · CNGuangzhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lung adenocarcinoma (LUAD), the most common histotype of lung cancer, may have variable prognosis due to molecular variations. The research strived to establish a prognostic model based on malignancy-related risk score (MRRS) in LUAD. Methods: We applied the single-cell RNA sequencing (scRNA-seq) data from Tumor Immune Single Cell Hub database to recognize malignancy-related geneset. Meanwhile, we extracted RNA-seq data from The Cancer Genome Atlas database. The GSE68465 and GSE72094 datasets from the Gene Expression Omnibus database were downloaded to validate the prognostic signature. Random survival forest analysis screened MRRS with prognostic significance. Multivariate Cox analysis was leveraged to establish the MRRS. Furthermore, the biological functions, gene mutations, and immune landscape were investigated to uncover the underlying mechanisms of the malignancy-related signature. In addition, we used qRT-PCR to explore the expression profile of MRRS-constructed genes in LUAD cells. Results: The scRNA-seq analysis revealed the markers genes of malignant celltype. The MRRS composed of 7 malignancy-related genes was constructed for each patient, which was shown to be an independent prognostic factor. The results of the GSE68465 and GSE72094 datasets validated MRRS's prognostic value. Further analysis demonstrated that MRRS was involved in oncogenic pathways, genetic mutations, and immune functions. Moreover, the results of qRT-PCR were consistent with bioinformatics analysis. Conclusion: Our research recognized a novel malignancy-related signature for predicting the prognosis of LUAD patients and highlighted a promising prognostic and treatment marker for LUAD patients.

Indexed as

gene signaturelung adenocarcinomamalignancyprognosisScRNA-seq

Identifiers

PMID37427142
PMCPMC10327591
OpenAlexW4381852591

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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.