Evidence map›Paper›PMID 34367284›Full record

ArticleJournal of oncology2021

Classification of Lung Adenocarcinoma Based on Immune Checkpoint and Screening of Related Genes.

Ting Zhou, Ping Yang, Sanyuan Tang, Zhongshan Zhu, Xiaobing Li, Zhou Yang, Ruoxia Wu, Xuefei Tian, Liang Li

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Co-Expression of MultipleInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

9 authors at 1 institution in 1 country.

Ting ZhouDepartment of Oncology, Brain Hospital of Hunan Province, Changsha 410007, Hunan Province, China.ORCID https://orcid.org/0000-0003-3685-0130
Ping YangDepartment of Psychiatry, Brain Hospital of Hunan Province, Clinical Medical College of Hunan University of Chinese Medicine, Changsha 410007, China.ORCID https://orcid.org/0000-0003-2375-0616
Sanyuan TangDepartment of Oncology, Brain Hospital of Hunan Province, Changsha 410007, Hunan Province, China.
Zhongshan ZhuDepartment of Oncology, Brain Hospital of Hunan Province, Changsha 410007, Hunan Province, China.
Xiaobing LiDepartment of Oncology, Brain Hospital of Hunan Province, Changsha 410007, Hunan Province, China.
Zhou YangDepartment of Oncology, Brain Hospital of Hunan Province, Changsha 410007, Hunan Province, China.
Ruoxia WuHunan Key Laboratory of TCM Prescription and Syndromes Translational Medicine, Hunan University of Chinese Medicine, Changsha, 410208, Hunan Province, China.ORCID https://orcid.org/0000-0003-3416-7514
Xuefei TianDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha, 410208, Hunan Province, China.ORCID https://orcid.org/0000-0002-8407-2268
Liang LiProvincial Key Laboratory of TCM Diagnostics, Hunan University of Chinese Medicine, Changsha 410208, Hunan Province, China.ORCID https://orcid.org/0000-0001-9994-4690
Hunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsLung adenocarcinoma (LUAD) cells could escape from the monitoring of immune cells and metastasize rapidly through immune escape. Therefore, we aimed to develop a method to predict the prognosis of LUAD patients based on immune checkpoints and their associated genes, thus providing guidance for LUAD treatment.

methodsGene sequencing data were downloaded from the Cancer Genome Atlas (TCGA) and analyzed by R software and R Bioconductor software package. Based on immune checkpoint genes, kmdist clustering in ConsensusClusterPlus R software package was utilized to classify LUAD. CIBERSORT was used to quantify the abundance of immune cells in LUAD samples. LM22 signature was performed to distinguish 22 phenotypes of human infiltrating immune cells. Gene set variation analysis (GSVA) was performed on immune checkpoint cluster and immune checkpoint score using GSVA R software package. The risk score was calculated by LASSO regression coefficient. Gene Ontology (GO), Hallmark, and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were performed. PROC was performed to generate the ROC curve and calculate the area under the curve (AUC).

resultsAccording to the immune checkpoint, LUAD was classified into clusters 1 and 2. Survival rate, immune infiltration patterns, TMB, and immune score were significantly different between the two clusters. Functional prediction showed that the functions of cluster 1 focused on apoptosis, JAK/STAT signaling pathway, TNF-

conclusionWe established a nine-gene signature based on immune checkpoints, which may contribute to the diagnosis, prognosis, and clinical treatment of LUAD.

Identifiers

PMID34367284
PMCPMC8337117
OpenAlexW3186427964

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.