Evidence map›Paper›PMID 32761562›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2020

Activation of dopamine receptor D1 inhibits glioblastoma tumorigenicity by regulating autophagic activity.

Kang Yang, Minghai Wei, Zhaofei Yang, Zhenfa Fu, Ruixue Xu, Cheng Cheng, Xi Chen, Sheng Chen, Eric Dammer, Weidong Le

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Cancer and neurotransmitter receptors.Chinese medical journal · 2025
    Review
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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

10 authors at 4 institutions in 2 countries.

Kang YangDalian Medical University, Dalian, People's Republic of China.
Minghai WeiDalian Medical University, Dalian, People's Republic of China.
Zhaofei YangLiaoning Provincial Center for Clinical Research on Neurological Diseases, The First Affiliated Hospital, Dalian Medical University, Dalian, People's Republic of China.
Zhenfa FuLiaoning Provincial Center for Clinical Research on Neurological Diseases, The First Affiliated Hospital, Dalian Medical University, Dalian, People's Republic of China.
Ruixue XuDepartment of Neurosurgery, The First Affiliated Hospital of Dalian Medical University, Dalian, People's Republic of China.
Cheng ChengLiaoning Provincial Center for Clinical Research on Neurological Diseases, The First Affiliated Hospital, Dalian Medical University, Dalian, People's Republic of China.
Xi ChenLiaoning Provincial Center for Clinical Research on Neurological Diseases, The First Affiliated Hospital, Dalian Medical University, Dalian, People's Republic of China.
Sheng ChenDepartment of Neurology, The Ruijin Hospital of Shanghai Jiao-Tong University School of Medicine, Shanghai, China.
Eric DammerEmory School of Medicine and Center for Neurodegenerative Disease, Atlanta, GA, USA.
Weidong LeLiaoning Provincial Center for Clinical Research on Neurological Diseases, The First Affiliated Hospital, Dalian Medical University, Dalian, People's Republic of China. wdle@sibs.ac.cn.
Dalian Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CNInstitute for Neurodegenerative Disorders · USShanghai Jiao Tong University · CN

Funding

Liaoning provincial key research project 2018225051National Natural Science Foundation of China 81430021National Natural Science Foundation of China 81771521
6 · The paper itself

Abstract

purposeRecent studies have reported important roles of dopamine receptors in the early development and progression of glioblastoma (GBM). Here, we tested the antitumor activity of a Dopamine receptor D1 (DRD1) agonist, either alone or in combination with temozolomide (TMZ) on GBM cells.

methodsImmunofluorescence, immunohistochemistry and Western blotting were used to detect dopamine receptor expression in primary human GBM tissues. In addition, clinical data of GBM patients downloaded from The Cancer Genome Atlas (TCGA) were analyzed. Image-based tracking analysis of LC3 using a mCherry-eGFP-LC3 plasmid was utilized to monitor autophagic flux. Transmission electron microscopy (TEM) was used to visualize aggregation of autophagosomes/autolysosomes. Finally, DRD1 agonist (SKF83959)-induced inhibition of GBM growth was assessed in vitro and in vivo.

resultsPositive DRD1 expression was observed in human GBM tissues and found to be related with a good clinical outcome. DRD1 activation specifically inhibited GBM cell growth and significantly disrupted autophagic flux, which led to tumor cell death. Moreover, we found that DRD1 agonist treatment inhibited auto-lysosomal degradation in GBM cells and that this process was calcium overload dependent and related to inhibition of mammalian target of rapamycin (mTOR). Finally, we found that DRD1 agonist and TMZ co-treatment yielded a synergistic therapeutic effect both in vivo and in vitro.

conclusionsFrom our data we conclude that DRD1 activation inhibits GBM cell growth and may serve as an alternative avenue for the design of future GBM therapies.

Indexed as

AutophagyAnimalsCalciumCarcinogenesisCell Line, TumorCell ProliferationGlioblastomaHumansIntracellular SpaceLysosomesMAP Kinase Signaling SystemMice, Inbred BALB CMice, NudeModels, BiologicalReceptors, Dopamine D1TemozolomideCalciumReceptors, Dopamine D1TemozolomideTOR Serine-Threonine KinasesAutophagyDopamine agonistDopamine receptorGlioblastomaTemozolomide

Identifiers

PMID32761562
PMCPMC12990682
OpenAlexW3047440828

What OpenQuestion holds

Textmetadata
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.