Evidence map›Paper›PMID 28891752›Full record

ArticleMonoclonal antibodies in immunodiagnosis and immunotherapy2017

Development of EMab-51, a Sensitive and Specific Anti-Epidermal Growth Factor Receptor Monoclonal Antibody in Flow Cytometry, Western Blot, and Immunohistochemistry.

Shunsuke Itai, Mika K Kaneko, Yuki Fujii, Shinji Yamada, Takuro Nakamura, Miyuki Yanaka, Noriko Saidoh, Saori Handa, Yao-Wen Chang, Hiroyoshi Suzuki and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Monoclonal antibodies in immunodiagnosis and immunotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. An End-to-endProceedings. IEEE International Conference on Healthcare Informatics · 2023
    Article
  2. Current Targeted Therapy for Metastatic Colorectal Cancer.International journal of molecular sciences · 2023
    Review
  3. A cancer-specific anti-podocalyxin monoclonal antibody (60-mGBiochemistry and biophysics reports · 2020
    Article
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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 3 institutions in 1 country.

Shunsuke Itai1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Mika K Kaneko1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Yuki Fujii3 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Shinji Yamada1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Takuro Nakamura1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Miyuki Yanaka1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Noriko Saidoh1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Saori Handa1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Yao-Wen Chang1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Hiroyoshi Suzuki4 Department of Pathology and Laboratory Medicine, Sendai Medical Center , Miyagi, Japan .
Hiroyuki Harada2 Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University , Tokyo, Japan .
Yukinari Kato1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Miyagi, Japan .
Tohoku University · JPTokyo Medical and Dental University · JPSendai Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epidermal growth factor receptor (EGFR) is a member of the human epidermal growth factor receptor (HER) family of receptor tyrosine kinases and is involved in cell growth and differentiation. EGFR homodimers or heterodimers with other HER members, such as HER2 and HER3, activate downstream signaling cascades in many cancers. In this study, we developed novel anti-EGFR monoclonal antibodies (mAbs) and characterized their efficacy in flow cytometry, Western blot, and immunohistochemical analyses. First, we expressed the full-length or ectodomain of EGFR in LN229 glioblastoma cells and then immunized mice with LN229/EGFR or ectodomain of EGFR, and performed the first screening using enzyme-linked immunosorbent assays. Subsequently, we selected mAbs according to their efficacy in flow cytometry (second screening), Western blot (third screening), and immunohistochemical (fourth screening) analyses. Among 100 mAbs, only one clone EMab-51 (IgG

Indexed as

AnimalsAntibodies, MonoclonalCell Line, TumorCell ProliferationErbB ReceptorsFlow CytometryGlioblastomaHumansImmunohistochemistryMiceMouth NeoplasmsSignal TransductionAntibodies, MonoclonalEGFR protein, humanErbB ReceptorsEGFRimmunohistochemistrymonoclonal antibodyoral cancer

Identifiers

PMID28891752
PMCPMC7001460
OpenAlexW2755413521

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.