Evidence map›Paper›PMID 31618934›Full record

ArticleCancers2019

Genetic and Lineage Classification of Glioma-Initiating Cells Identifies a Clinically Relevant Glioblastoma Model.

Norihiko Saito, Nozomi Hirai, Kazuya Aoki, Sho Sato, Ryo Suzuki, Yu Hiramoto, Satoshi Fujita, Haruo Nakayama, Morito Hayashi, Takatoshi Sakurai and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 10 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

11 authors at 2 institutions in 1 country.

Norihiko SaitoDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. bsaitob@med.toho-u.ac.jp.
Nozomi HiraiDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. nozomi.hirai@med.toho-u.ac.jp.
Kazuya AokiDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. kaoki@med.toho-u.ac.jp.
Sho SatoDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. sho.sato@med.toho-u.ac.jp.
Ryo SuzukiDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. ryo.suzuki@med.toho-u.ac.jp.
Yu HiramotoDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. yu.hiramoto@med.toho-u.ac.jp.
Satoshi FujitaDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. satoshi.fujita@med.toho-u.ac.jp.
Haruo NakayamaDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. haruonakayama@med.toho-u.ac.jp.
Morito HayashiDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. morito@med.toho-u.ac.jp.
Takatoshi SakuraiDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. cherry@med.toho-u.ac.jp.
Satoshi IwabuchiDepartment of Neurosurgery, Toho University Ohashi Medical Center, Tokyo 153-8515, Japan. iwabuchi@med.toho-u.ac.jp.
Toho University · JPToho University Ohashi Medical Center · JP

Funding

JSPS KAKENHI 15K19980
6 · The paper itself

Abstract

The Cancer Genome Atlas (TCGA) project described a robust gene expression-based molecular classification of glioblastoma (GBM), but the functional and biological significance of the subclasses has not been determined. The present comprehensive analysis of 25 glioma-initiating cell (GIC) lines classifies GIC lines into four subtypes (classical, mesenchymal, proneural, and neural) that are closely related to the TCGA GBM subclasses and display distinct lineage characteristics and differentiation behavior that recapitulate neural development. More importantly, the GIC subtypes exhibit distinct biological phenotypes in relation to self-renewal capacity, proliferation, invasiveness, and angiogenic potential in vitro and in vivo. In addition, the GIC subtypes exhibit divergent patterns of signaling pathway activation and deactivation of the Wnt, Notch, and TGF-β pathways. These results will improve drug discovery targeting certain genetic mutation in glioblastoma and improve the development of precision medicine.

Indexed as

glioblastomaglioma initiating cellmolecular classificationThe Cancer Genome Atlas

Identifiers

PMID31618934
PMCPMC6826962
OpenAlexW2980729449

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.