Evidence map›Paper›PMID 32793702›Full record

ArticleAnnals of translational medicine2020

Artesunate exerts anti-prolactinoma activity by inhibiting mitochondrial metabolism and inducing apoptosis.

Weiyu Zhang, Qiu Du, Piaopiao Bian, Zheng Xiao, Xin Wang, Yajuan Feng, Hou Feng, Ziyan Zhu, Nailin Gao, Diming Zhu and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Anti-tumor mechanism of artesunate.Frontiers in pharmacology · 2024
    Review
  3. Review
  4. Article
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

12 authors at 5 institutions in 1 country.

Weiyu ZhangDepartment of Neurosurgery, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.
Qiu DuDepartment of Neurosurgery, The Affiliated Hospital of Yangzhou University, Yangzhou, China.
Piaopiao BianDepartment of Pathology, The Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Zheng XiaoDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xin WangDepartment of Histology and Embryology, Guangdong Pharmaceutical University, Guangzhou, China.
Yajuan FengDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Hou FengDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Ziyan ZhuDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Nailin GaoDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Diming ZhuDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiang FanDepartment of Neurosurgery, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.
Yonghong ZhuDepartment of Neurosurgery and Pituitary Tumor Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CNFifth Affiliated Hospital of Sun Yat-sen University · CNGuangdong Pharmaceutical University · CNThird Affiliated Hospital of Guangzhou Medical University · CNYangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProlactinoma is the most common hormone-secreting pituitary adenoma. Dopamine receptor agonists (DAs) are effective in reducing prolactin levels and tumor mass, but some prolactinoma patients are resistant to DAs. Treating patients with DA-resistant prolactinoma is challenging. In this study, we examined the anti-prolactinoma effect of artesunate (ART), a potential new treatment option for prolactinoma, and its mechanism of action.

methodsCell Counting Kit-8 (CCK8) and flow cytometry were used to detect the effect of ART on the proliferation, cycle, and apoptosis of rat pituitary adenoma cell line MMQ. The subcellular localization of ART was observed using confocal fluorescence microscopy. The JC-1 mitochondrial membrane potential (MMP) detection and Seahorse assays were used to detect the effect of ART on mitochondrial function. Real-time quantitative polymerase chain reaction (RT-qPCR) and Western blot analysis were used to detect the effect of ART on the expression of prolactin (PRL) and apoptosis-related proteins. A mouse xenograft model of prolactinoma was used to detect the inhibitory effect of ART on MMQ

resultsART specifically inhibited MMQ proliferation and PRL synthesis, induced G0/G1 phase arrest and apoptosis

conclusionsART has a strong inhibitory effect on prolactinoma both

Indexed as

apoptosisArtesunate (ART)metabolismmitochondrial membrane potential (MMP)prolactinoma

Identifiers

PMID32793702
PMCPMC7396798
OpenAlexW3043006901

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.