Evidence map›Paper›PMID 32207044›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2020

Dp44mT, an iron chelator, suppresses growth and induces apoptosis via RORA-mediated NDRG2-IL6/JAK2/STAT3 signaling in glioma.

Jinpeng Zhou, Yang Jiang, Junshuang Zhao, Haiying Zhang, Jinlong Fu, Peng Luo, Yanju Ma, Dan Zou, Huiling Gao, Jiangfeng Hu and 2 more

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 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 61 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

12 authors at 7 institutions in 1 country.

Jinpeng ZhouDepartment of Neurosurgery, the First Hospital of China Medical University, NO.155, North Nanjing Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
Yang JiangDepartment of Neurosurgery, the First Hospital of China Medical University, NO.155, North Nanjing Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
Junshuang ZhaoDepartment of Neurosurgery, the First Hospital of China Medical University, NO.155, North Nanjing Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
Haiying ZhangInternational Education College, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Jinlong FuDepartment of Neurosurgery, the First Hospital of China Medical University, NO.155, North Nanjing Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
Peng LuoDepartment of Neurosurgery, the First Hospital of China Medical University, NO.155, North Nanjing Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
Yanju MaDepartment of Oncology, Liaoning Province Tumor Hospital, Shenyang, Liaoning, China.
Dan ZouThe First Laboratory of Cancer Institute, the First Hospital of China Medical University, Shenyang, Liaoning, China.
Huiling GaoCollege of Life and Health Sciences, Northeastern University, Shenyang, Liaoning, China.
Jiangfeng HuDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ye ZhangThe First Laboratory of Cancer Institute, the First Hospital of China Medical University, Shenyang, Liaoning, China.
Zhitao JingDepartment of Neurosurgery, the First Hospital of China Medical University, NO.155, North Nanjing Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China. ztjing@cmu.edu.cn.
First Hospital of China Medical University · CNChina Medical University · CNLiaoning Cancer Hospital & Institute · CNLiaoning University of Traditional Chinese Medicine · CNNortheastern University · CNShanghai First People's Hospital · CNShanghai Jiao Tong University · CN

Funding

Fund for Scientific Research of The First Hospital of China Medical University FHCMU- FSRLiaoning BaiQianWan Talents Program 2019-B45National Natural Science Foundation of China 30901736National Natural Science Foundation of China 81101917National Natural Science Foundation of China 81270036Natural Science Foundation of Liaoning Province 20170541022Science and Technology Plan Project of Shenyang City 18-014-4-11Shanghai Sailing Program 19YF1439000the Plan to Focus on Research and Development from Science and Technology project of Liaoning Province 2017225029
6 · The paper itself

Abstract

purposeThe iron-chelating agent di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone (Dp44mT) has been found to inhibit cell growth and to induce apoptosis in several human cancers. However, its effects and mechanism of action in glioma are unknown.

methodsHuman glioma cell line LN229 and patient-derived glioma stem cells GSC-42 were applied for both in vitro and in vivo xenograft nude mouse experiments. The anti-tumor effects of Dp44mT were assessed using MTS, EdU, TUNEL, Western blotting, qRT-PCR, luciferase reporter, chromatin immunoprecipitation and immunohistochemical assays.

resultsWe found that Dp44mT can upregulate the expression of the anti-oncogene N-myc downstream-regulated gene (NDRG)2 by directly binding to and activating the RAR-related orphan receptor (ROR)A. In addition, we found that NDRG2 overexpression suppressed inflammation via activation of interleukin (IL)-6/Janus kinase (JAK)2/signal transducer and activator of transcription (STAT)3 signaling.

conclusionsOur data indicate that Dp44mT may serve as an effective drug for the treatment of glioma by targeting RORA and enhancing NDRG2-mediated IL-6/JAK2/STAT3 signaling.

Indexed as

AnimalsApoptosisCarcinogenesisCell Line, TumorCell ProliferationFemaleGliomaHumansInterleukin-6Iron Chelating AgentsJanus Kinase 2Mice, Inbred BALB CModels, BiologicalNeoplastic Stem CellsNuclear Receptor Subfamily 1, Group F, Member 1Signal Transductiondi-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazoneInterleukin-6Iron Chelating AgentsJAK2 protein, humanJanus Kinase 2NDRG2 protein, humanNuclear Receptor Subfamily 1, Group F, Member 1RORA protein, humanSTAT3 protein, humanSTAT3 Transcription FactorThiosemicarbazonesTumor Suppressor ProteinsApoptosisDp44mTGliomaIL6/JAK2/STAT3NDRG2ProliferationRORA

Identifiers

PMID32207044
PMCPMC12990703
OpenAlexW3012838993

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.