Evidence map›Paper›PMID 36529788›Full record

ArticleEuropean journal of medical research2022

Targeting regulation of VEGF by BPTF in non-small cell lung cancer and its potential clinical significance.

Meng Dai, Chunyu Hua, Mingqin Wang, Li Gao, Ling Jiang, Yuan Liu

Open access · goldAbstract read
In one paragraph

Article in European journal of medical research, 2022. 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
0.4field-weighted citation impact, top 40% 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, 5 citations in OpenAlex.

  1. Trial
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  5. Review
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

6 authors at 3 institutions in 1 country.

Meng Dai *Dalian Municipal Central Hospital, Dalian University of Technology, Dalian, 116011, China. 446916982@qq.com.
Chunyu Hua *Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Mingqin Wang *Dalian Municipal Central Hospital, Dalian University of Technology, Dalian, 116011, China.
Li GaoDalian Municipal Central Hospital, Dalian University of Technology, Dalian, 116011, China.
Ling JiangDalian Municipal Central Hospital, Dalian University of Technology, Dalian, 116011, China.
Yuan LiuDalian Municipal Central Hospital, Dalian University of Technology, Dalian, 116011, China.
Dalian University of Technology · CNDalian Municipal Central Hospital · CNDalian Medical University · CN

Funding

Dalian Municipal Health and Family Planning Commission Project 20161114
6 · The paper itself

Abstract

purposeVEGF facilitates tumor angiogenesis, and bevacizumab targeting VEGF is used in anti-tumor therapy. It is meaningful to clarify the upstream regulatory mechanism of VEGF. BPTF is important in chromosomal remodeling, and promotes the progression of tumors. However, its role in promoting tumor angiogenesis by targeting VEGF has not been fully reported. This study aims to elucidate the expression regulation of VEGF by BPTF and its clinical significance in NSCLC.

methods1. BPTF siRNA and shRNA plasmids were used to reduce the expression of BPTF by transfection in vivo and in vitro. BPTF, VEGF and CD144 expressions were examined by immunofluorescence and Western Blot. 2. The expressions of BPTF, VEGF, CD144 and CD31 were detected in lung adenocarcinoma samples by immunofluorescence, Western blot and immunohistochemical staining. 3. 26 lung adenocarcinoma patients treated by bevacizumab were divided into 2 groups according to the treatment efficacy. BPTF and VEGF expressions were analyzed.

results1. BPTF knockdown inhibited the expression of VEGF and CD144 in vivo and in vitro. 2. Compared with para-cancer tissues, BPTF, VEGF, CD144 and CD31 were highly expressed in lung adenocarcinoma. 3. In 75 lung adenocarcinoma specimens, BPTF and VEGF overexpression was correlated with lymph node metastasis and clinical stage. The 5-year survival rate of patients with BPTF and VEGF low expression was higher, and BPTF expression was positively correlated with VEGF expression. 4. Among 26 patients treated with bevacizumab, the patients with BPTF overexpression are more sensitive to the treatment.

conclusionsBPTF positively regulates VEGF expression and its high expression predicts a better efficacy of bevacizumab treatment in NSCLC.

Indexed as

Adenocarcinoma of LungCarcinoma, Non-Small-Cell LungLung NeoplasmsAntigens, NuclearBevacizumabBromodomain Containing ProteinsClinical RelevanceHumansNerve Tissue ProteinsRNA, Small InterferingTranscription FactorsVascular Endothelial Growth Factor AAntigens, NuclearBevacizumabBromodomain Containing Proteinsfetal Alzheimer antigenNerve Tissue ProteinsRNA, Small InterferingTranscription FactorsVascular Endothelial Growth Factor AVEGFA protein, humanAngiogenesisBevacizumabBiomarkersBPTFNSCLCVEGF

Identifiers

PMID36529788
PMCPMC9762081
OpenAlexW4312065494

What OpenQuestion holds

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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.