Evidence map›Paper›PMID 33854716›Full record

ArticleJournal of dental sciences2021

Mining TCGA database for prognostic genes in head and neck squamous cell carcinoma microenvironment.

Qiu-Chi Ran, Sheng-Rong Long, Yan Ye, Chen Xie, Zhuo-Lin XuXiao, Yu-Song Liu, Hong-Xia Pang, Diwas Sunchuri, Nai-Chia Teng, Zhu-Ling Guo

Open access · goldAbstract read
In one paragraph

Article in Journal of dental sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 11 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

10 authors at 4 institutions in 2 countries.

Qiu-Chi RanSchool of Dentistry, Hainan Medical University, Hainan, China.
Sheng-Rong LongDepartment of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Yan YeTechnology Section, Duoyi Network, Wuhan, China.
Chen XieSchool of Dentistry, Hainan Medical University, Hainan, China.
Zhuo-Lin XuXiaoSchool of Dentistry, Hainan Medical University, Hainan, China.
Yu-Song LiuSchool of Dentistry, Hainan Medical University, Hainan, China.
Hong-Xia PangDepartment of Dentistry, The First Affiliated Hospital of Hainan Medical University, Hainan, China.
Diwas SunchuriSchool of Dentistry, Hainan Medical University, Hainan, China.
Nai-Chia TengSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
Zhu-Ling GuoSchool of Dentistry, Hainan Medical University, Hainan, China.
Hainan Medical University · CNChina Medical University · CNFirst Hospital of China Medical University · CNTaipei Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background/purposeHead and neck squamous cell carcinoma (HNSCC) is one of the most common malignant tumors. The aim of this study was to elucidate the effect of tumor microenvironment-related genes on the prognosis of HNSCC and to obtain tumor microenvironment-related genes that can predict poor prognosis in HNSCC patients. MATERIALS AND

methodsThe ESTIMATE algorithm was applied to the HNSCC transcriptomic data downloaded from the TCGA (The cancer genome atlas), and then the samples were divided into two groups: high and low immune scoring groups, and high and low basal scoring groups to screen for differentially expressed genes (DEGs) associated with poor patient outcomes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis was performed to explore the potential functions of DEGs, and then to explore the potential prognostic value of individual DEGs. The results of survival analysis between DEGs and overall survival (OS) to explore tumor microenvironment-related genes relevant to the prognosis of HNSCC patients.

resultsFifty-nine tumor microenvironment-related genes were screened for association of OS with HNSCC (P < 0.05). The GO and KEGG enrichment analysis showed that the selected DEGs may mediate immune response, extracellular matrix, and immunoglobulin binding via neutrophil activation in HNSCC. Six of these DEGs, GIMAP6, SELL, TIFAB, KCNA3, P2RY8 and CCR4 were most significantly associated with OS (P < 0.001).

conclusionWe identified six tumor microenvironment-related genes that were significantly associated with poor prognosis in HNSCC. These genes may inspire researchers to discover new targets and approaches for HNSCC treatment.

Indexed as

HNSCCImmune scoresTCGATumor microenvironment

Identifiers

PMID33854716
PMCPMC8025193
OpenAlexW3092672648

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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.