Evidence map›Paper›PMID 35028857›Full record

ArticleMolecular biology reports2022

High expression of HOXB3 predicts poor prognosis and correlates with tumor immunity in lung adenocarcinoma.

Ming Yan, Xiaojun Yin, Luan Zhang, Yuanbo Cui, Xiwen Ma

Abstract read
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Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

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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

12 citing papers in PubMed, 13 citations in OpenAlex.

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  9. Classification of bladder cancer based on immune cell infiltration and construction of a risk prediction model for prognosis.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2023
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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

5 authors at 3 institutions in 1 country.

Ming Yan *Basic Medical College, Zhengzhou University, Zhengzhou, 450001, China.
Xiaojun Yin *Kunshan Second People's Hospital, Suzhou, 215300, China.
Luan ZhangJiangsu Mai Jian Biotechnology Development Company, Wuxi, 214135, China.
Yuanbo CuiTranslational Medicine Center, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, 450007, China. cuiyuanbo18@126.com.
Xiwen MaDepartment of Endocrinology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, 450007, China. 15515964198@163.com.
Zhengzhou Central Hospital · CNJiangsu University · CNZhengzhou University · CN

Funding

Science and Technology Department of Henan Province LHGJ20200765Science and Technology Department of Henan Province SB201903032Science and Technology Department of Henan Province SBGJ202003053
6 · The paper itself

Abstract

backgroundLung adenocarcinoma (LUAD) is one of the most prevalent human cancers worldwide. The homeobox-B (HOXB) gene cluster has been reported to contribute to cancer development. Nevertheless, the expression status, clinical significance and biological role of HOXB genes in LUAD remain largely unclear. METHODS AND

resultsThis study comprehensively investigated the transcriptional levels and prognostic values of the HOXB genes in LUAD based on The Cancer Genome Atlas (TCGA) database. Flow cytometry, CCK-8, and Transwell assays were used for detecting apoptosis, proliferation, and migration, respectively. We discovered that eight members of the HOXB cluster genes (HOXB2, HOXB3, HOXB4, HOXB6, HOXB7, HOXB8, HOXB9, and HOXB13) were dysregulated in LUAD tumor tissues. Increased expression of HOXB3, HOXB6, HOXB7, HOXB8, or HOXB9 was independently associated with unsatisfactory overall survival (OS) in LUAD patients. In addition, a high level of HOXB3 also predicted poor patient relapse-free survival (RFS), suggesting that HOXB3 may play a vital role in the progression of LUAD compared to other members of the HOXB cluster. Additionally, further analysis by TIMER and TISIDB algorithms revealed that HOXB3 was positively correlated with a panel of immune checkpoint molecules (ICMs), tumor-infiltrating lymphocytes (TILs), and tumor immune regulators (TIRs). Gene enrichment analysis based on KEGG showed that HOXB3 was closely associated with multiple tumor-related biological processes and signaling pathways. Functionally, the in vitro experiments revealed that depletion of HOXB3 significantly alleviated the resistance of LUAD cells to apoptosis, and suppressed cell proliferation and migration.

conclusionOur study suggests that HOXB3 may play an oncogenic role in LUAD and correlate with tumor immunity.

Indexed as

Adenocarcinoma of LungLung NeoplasmsGene Expression Regulation, NeoplasticGenes, HomeoboxHomeodomain ProteinsHumansNeoplasm Recurrence, LocalTranscription FactorsHomeodomain ProteinsHOXB2 protein, humanHoxB3 protein, humanHOXB7 protein, humanHOXB9 protein, humanTranscription FactorsHomeobox-B cluster genesHOXB3Lung adenocarcinomaTCGATumor immunity

Identifiers

PMID35028857
OpenAlexW4205866349

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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.