Evidence map›Paper›PMID 35402180›Full record

ArticleTranslational cancer research2022

Induction of ligustrazine apoptosis of A549 cells through activation of death receptor pathway.

Wei Zheng, Jihua Yang, Juyi Wen, Junzhao Sun, Jing Wang, Xinhong Zhang, Xia Zhang, Xiangfei Zhao, Henghu Fang, Qi Zhu and 11 more

Open access · diamondAbstract read
In one paragraph

Article in Translational cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

21 authors at 1 institution in 1 country.

Wei ZhengSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Jihua YangDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Juyi WenDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Junzhao SunDepartment of Neurosurgery, Chinese PLA General Hospital, Beijing, China.
Jing WangDepartment of General Medicine, the First Medical Center of PLA General Hospital, Beijing, China.
Xinhong ZhangSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Xia ZhangSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Xiangfei ZhaoSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Henghu FangSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Qi ZhuSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Shanshan WuSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Zejun LuSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Heng SunSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Rugang ZhaoSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Siyuan HuaiSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Lipin GaoDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Yongzhen LiuDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Jingjiao LiDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Gaowa GuanDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Wei YangDepartment of Oncology, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Yi HuSenior Department of Oncology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The aim of this study was to evaluate the effect of ligustrazine on the apoptosis of A549 cells and clarify the mechanism of ligustrazine-induced apoptosis. Methods: Ligustrazine was prepared with medium according to the gradient concentration. Based on a cytotoxicity test, 3 different concentrations of ligustrazine were selected to form low, medium, and high groups, with a 0 mg/mL dose used as the control. The apoptosis degree and Fas (Fas cell surface death receptor) and Fas-L (Fas Ligand) expression were detected by flow cytometry and quantitative polymerase chain reaction (qPCR), respectively; meanwhile, the activity of caspase 8 and caspase 3 was analyzed by enzyme-linked immunosorbent assay (ELISA) and qPCR, respectively. Results: After 24 hours of ligustrazine administration, the survival rate of A549 cells decreased with the increase of drug concentration, while the rate of apoptosis increased with the increase of drug concentration. Meanwhile, Fas and Fas-L expression was found to be significantly increased at both the gene and protein level, which was positively correlated with drug concentration. Furthermore, the expression of caspase 8 and caspase 3 was positively correlated with the concentration of ligustrazine, and there was significant difference compared with the control group. Conclusions: Ligustrazine can induce the apoptosis of A549 cells via the upregulation of Fas- and caspase-activating death receptor pathway expression.

Indexed as

caspasecell apoptosisFasFas-LLigustrazine

Identifiers

PMID35402180
PMCPMC8990827
OpenAlexW4220788910

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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.