Evidence map›Paper›PMID 37694790›Full record

ArticleCurrent medicinal chemistry2024

Identifying Luteolin as a Potential Drug for Treating Lung Adenocarcinoma with COVID-19 Affection based on Integration Analysis of Pharmacology and Transcriptome.

Ping Peng, Na Li, Ni Zhang, Xiangning Fu, Shu Peng, Yujie Zhao, Bo Ai

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Article in Current medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 2 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

7 authors at 2 institutions in 2 countries.

Ping PengDepartment of thoracic surgery, Tongji Hospital, Wuhan, 430000, China.
Na LiShenzhen Engineering Center for Translational Medicine of Precision Cancer Immunodiagnosis and Therapy, Yuce Biotechnology Co., Ltd, Shenzhen, 518000, China.
Ni ZhangDepartment of thoracic surgery, Tongji Hospital, Wuhan, 430000, China.
Xiangning FuDepartment of thoracic surgery, Tongji Hospital, Wuhan, 430000, China.
Shu PengDepartment of thoracic surgery, Tongji Hospital, Wuhan, 430000, China.
Yujie ZhaoShenzhen Engineering Center for Translational Medicine of Precision Cancer Immunodiagnosis and Therapy, Yuce Biotechnology Co., Ltd, Shenzhen, 518000, China.
Bo AiDepartment of thoracic surgery, Tongji Hospital, Wuhan, 430000, China.
Tongji Hospital · CNPrecision for Medicine (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung adenocarcinoma (LUAD) is a major type of lung cancer worldwide, and under the pandemic coronavirus disease 2019 (COVID-19), its cancer burden is enlarged. This study aimed to explore potential drug targets and potential drugs for developing effective treatments for patients with both lung cancer and COVID-19.

methodsThe interaction network of molecule compounds-target genes was constructed based on Traditional Chinese Medicines (TCMs) and gene expression data from public databases. The potential effectiveness of drugs was analyzed by molecular docking and molecular dynamics simulation. Western blot, transfection assay, Immunohistochemistry (IHC) staining, and flow cytometry were performed to investigate the function of HSP90AA1 in LUAD cells.

resultEight target genes (GSK3B, HMOX1, HSP90AA1, ICAM1, MAPK1, PLAU, RELA and TNFSF15.) were identified, and two of them (HSP90AA1 and RELA) were significantly associated with LUAD prognosis. Luteolin was discovered to bind with HSP90AA1. Moreover,

conclusionHSP90AA1 was a target gene for further designing effective drugs for LUAD patients. Luteolin was a potential drug for treating patients with both LUAD and COVID-19.

Indexed as

Adenocarcinoma of LungCOVID-19COVID-19 Drug TreatmentLung NeoplasmsLuteolinMolecular Docking SimulationSARS-CoV-2A549 CellsAntineoplastic AgentsApoptosisCell ProliferationHSP90 Heat-Shock ProteinsHumansMedicine, Chinese TraditionalMolecular Dynamics SimulationTranscription Factor RelAAntineoplastic AgentsHSP90AA1 protein, humanHSP90 Heat-Shock ProteinsLuteolinRELA protein, humanTranscription Factor RelAcoronavirus disease 2019drug targetsHSP90AA1Lung adenocarcinomaluteolin.tumor microenvironment

Identifiers

PMID37694790
OpenAlexW4386593180

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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.