Evidence map›Paper›PMID 27788029›Full record

ArticleMonoclonal antibodies in immunodiagnosis and immunotherapy2016

Establishment of Anti-Human ATRX Monoclonal Antibody AMab-6.

Satoshi Ogasawara, Yuki Fujii, Mika K Kaneko, Hiroharu Oki, Hemragul Sabit, Mitsutoshi Nakada, Hiroyoshi Suzuki, Koichi Ichimura, Takashi Komori, Yukinari Kato

Open access · hybridAbstract read
In one paragraph

Article in Monoclonal antibodies in immunodiagnosis and immunotherapy, 2016. 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
0.8field-weighted citation impact, top 25% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Development of RAP Tag, a Novel Tagging System for Protein Detection and Purification.Monoclonal antibodies in immunodiagnosis and immunotherapy · 2017
    Article
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 1 country.

Satoshi Ogasawara1 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Sendai, Japan .
Yuki Fujii1 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Sendai, Japan .
Mika K Kaneko1 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Sendai, Japan .
Hiroharu Oki1 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Sendai, Japan .
Hemragul Sabit2 Department of Neurosurgery, Graduate School of Medical Science, Kanazawa University , Kanazawa, Japan .
Mitsutoshi Nakada2 Department of Neurosurgery, Graduate School of Medical Science, Kanazawa University , Kanazawa, Japan .
Hiroyoshi Suzuki3 Department of Pathology and Laboratory Medicine, Sendai Medical Center , Sendai, Japan .
Koichi Ichimura4 Division of Brain Tumor Translational Research, National Cancer Center Research Institute , Tokyo, Japan .
Takashi Komori5 Department of Neuropathology, Tokyo Metropolitan Neurological Hospital , Tokyo, Japan .
Yukinari Kato1 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Sendai, Japan .
Tohoku University · JPKanazawa University · JPSendai Medical Center · JPTokyo Metropolitan Neurological Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gliomas are the most frequently occurring brain tumors with a heterogeneous molecular background. The molecular subgrouping of gliomas more prognostically stratifies patients into distinct groups compared with conventional histological classification. The most important molecules for the subtype diagnosis of diffuse gliomas are mutations of isocitrate dehydrogenase (IDH), TERT promoter, and α-thalassemia/mental-retardation-syndrome-X-linked (ATRX) and the codeletion of 1p/19q. Among them, IDH and ATRX mutations can be diagnosed using specific monoclonal antibodies (mAbs). We have developed many mAbs against IDH mutants, including HMab-1/HMab-2 against IDH1-R132H and multispecific mAbs MsMab-1/MsMab-2 against IDH1/2 mutations. In contrast, highly sensitive mAbs against ATRX remain to be established. In this study, we immunized mice with recombinant human ATRX and developed a novel mAb, AMab-6. The dissociation constant of AMab-6 was determined to be 9.7 × 10

Indexed as

AnimalsAntibodies, MonoclonalAntibody SpecificityBiomarkers, TumorDNA HelicasesGene Expression Regulation, NeoplasticGliomaHumansIsocitrate DehydrogenaseMiceMutationNuclear ProteinsX-linked Nuclear ProteinAntibodies, MonoclonalATRX protein, humanBiomarkers, TumorDNA HelicasesIsocitrate DehydrogenaseNuclear ProteinsX-linked Nuclear ProteinATRXgliomaimmunohistochemistry

Identifiers

PMID27788029
PMCPMC5160166
OpenAlexW2560401729

What OpenQuestion holds

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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.