Evidence map›Paper›PMID 31705593›Full record

ArticleCancer science2020

Osteosarcoma-initiating cells show high aerobic glycolysis and attenuation of oxidative phosphorylation mediated by LIN28B.

Emi Mizushima, Tomohide Tsukahara, Makoto Emori, Kenji Murata, Asuka Akamatsu, Yuji Shibayama, Shuto Hamada, Yuto Watanabe, Mitsunori Kaya, Yoshihiko Hirohashi and 6 more

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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

30 citing papers in PubMed, 39 citations in OpenAlex.

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  14. Cancer/Testis Antigens as Targets for RNA-Based Anticancer Therapy.International journal of molecular sciences · 2023
    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

16 authors at 1 institution in 1 country.

Emi MizushimaDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Tomohide TsukaharaDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0002-3678-4359
Makoto EmoriDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Kenji MurataDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Asuka AkamatsuDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Yuji ShibayamaDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Shuto HamadaDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Yuto WatanabeDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Mitsunori KayaHitsujigaoka Hospital, Sapporo, Japan.
Yoshihiko HirohashiDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0002-0608-3914
Takayuki KanasekiDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Munehide NakatsugawaDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Terufumi KuboDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Toshihiko YamashitaDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Noriyuki SatoDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Toshihiko TorigoeDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Sapporo Medical University · JP

Funding

a Grant-In-Aid of Ono Cancer Research Fund 2017-3Japan Society for the Promotion of Science 17H01540Japan Society for the Promotion of Science 25462344the Cell Science Research FoundationThe Takeda Science Foundation
6 · The paper itself

Abstract

Osteosarcoma (OS) is a highly malignant bone tumor and the prognosis for non-responders to chemotherapy remains poor. Previous studies have shown that human sarcomas contain sarcoma-initiating cells (SIC), which have the characteristics of high tumorigenesis and resistance to chemotherapy. In the present study, we characterized SIC of a novel OS cell line, screened for SIC-related genes, and tried to regulate the proliferation of OS by metabolic interference. Initially, we established a new human OS cell line (OS13) and isolated clones showing higher tumorigenesis as SIC (OS

Indexed as

AnimalsBone NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGlycolysisHumansMaleMiceMice, Inbred NODOsteosarcomaOxidative PhosphorylationPlacentaPregnancyLIN28B protein, humanRNA-Binding ProteinsRNA, Messengerglycolysisosteosarcomasarcoma stem celltestis antigenWarburg effect

Identifiers

PMID31705593
PMCPMC6942429
OpenAlexW2987668306

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.