Evidence map›Paper›PMID 32495467›Full record

ArticleCancer science2020

Polyethylene glycol derivative 9bw suppresses growth of neuroblastoma cells by inhibiting oxidative phosphorylation.

Eri Nagasaki-Maeoka, Kazuhiro Ikeda, Ken-Ichi Takayama, Takayuki Hirano, Yoshiaki Ishizuka, Tsugumichi Koshinaga, Naoya Tsukune, Tadateru Takayama, Satoshi Inoue, Kyoko Fujiwara

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 55% 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

3 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

10 authors at 3 institutions in 1 country.

Eri Nagasaki-MaeokaDepartment of Pediatric Surgery, Nihon University School of Medicine, Itabashi, Japan.
Kazuhiro IkedaDivision of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Hidaka, Japan.
Ken-Ichi TakayamaDepartment of Systems Aging Science and Medicine, Tokyo Metropolitan Institute of Gerontology, Itabashi-ku, Japan.
Takayuki HiranoDepartment of Pediatric Surgery, Nihon University School of Medicine, Itabashi, Japan.
Yoshiaki IshizukaDepartment of Pediatric Surgery, Nihon University School of Medicine, Itabashi, Japan.
Tsugumichi KoshinagaDepartment of Pediatric Surgery, Nihon University School of Medicine, Itabashi, Japan.
Naoya TsukuneDepartment of Periodontology, Nihon University School of Dentistry, Chiyoda, Japan.
Tadateru TakayamaDivision of General Medicine, Department of Medicine, Nihon University School of Medicine, Itabashi, Japan.
Satoshi InoueDivision of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Hidaka, Japan.ORCID https://orcid.org/0000-0003-1247-3844
Kyoko FujiwaraDivision of General Medicine, Department of Medicine, Nihon University School of Medicine, Itabashi, Japan.ORCID https://orcid.org/0000-0002-1751-7968
Nihon University · JPTokyo Metropolitan Institute of Gerontology · JPSaitama Medical University · JP

Funding

JSPS Kakenhi 18K07275JSPS Kakenhi 19K24131
6 · The paper itself

Abstract

Neuroblastoma (NB) is a childhood malignancy originating from the sympathetic nervous system, and accounts for approximately 15% of all pediatric cancer-related deaths. As the 5-y survival rate of patients with high-risk NB is <50%, novel therapeutic strategies for NB patients are urgently required. Nonaethylene glycol mono('4-iodo-4-biphenyl)ester (9bw) is a polyethylene glycol derivative, synthesized by modifying a compound originally extracted from filamentous bacteria. Although 9bw shows remarkable inhibition of tumor cell growth, the underlying mechanisms remain unclear. Here, we examined the efficacy of 9bw on human NB-derived cells, and investigated the molecular mechanisms underlying the cytotoxic effects of 9bw on these cells. Our results indicated that 9bw induced cell death in NB cells by decreasing the production of ATP. Metabolome analysis and measurement of oxygen consumption indicated that 9bw markedly suppressed oxidative phosphorylation (OXPHOS). Further analyses indicated that 9bw inhibited the activity of mitochondrial respiratory complex I. Moreover, we showed that 9bw inhibited growth of NB in vivo. Based on the results of the present study, 9bw is a good candidate as a novel agent for treatment of NB.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCell SurvivalElectron Transport Complex IEstersFemaleHumansMiceMitochondriaNeuroblastomaOxidative PhosphorylationPolyethylene GlycolsXenograft Model Antitumor AssaysAntineoplastic AgentsElectron Transport Complex IEstersPolyethylene Glycolsanticancer drugmitochondrial respiratory complex Ineuroblastomaoxidative phosphorylationpolyethylene glycol derivative

Identifiers

PMID32495467
PMCPMC7419032
OpenAlexW3029879007

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.