Evidence map›Paper›PMID 28700270›Full record

ArticleMonoclonal antibodies in immunodiagnosis and immunotherapy2017

H

Shunsuke Itai, Yuki Fujii, Mika K Kaneko, Shinji Yamada, Takuro Nakamura, Miyuki Yanaka, Noriko Saidoh, Yao-Wen Chang, Saori Handa, Maki Takahashi and 3 more

Abstract 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. A cancer-specific anti-podocalyxin monoclonal antibody (60-mGBiochemistry and biophysics reports · 2020
    Article
  8. HExperimental and therapeutic medicine · 2020
    Article
  9. Article
  10. 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

13 authors.

Shunsuke Itai1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Yuki Fujii3 Department of Regional Innovation, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Mika K Kaneko1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Shinji Yamada1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Takuro Nakamura1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Miyuki Yanaka1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Noriko Saidoh1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Yao-Wen Chang1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Saori Handa1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .
Maki Takahashi4 Department of Pathology and Laboratory Medicine, Sendai Medical Center , Miyagino, Miyagino-ku, Sendai, Miyagi, Japan .
Hiroyoshi Suzuki4 Department of Pathology and Laboratory Medicine, Sendai Medical Center , Miyagino, Miyagino-ku, Sendai, Miyagi, Japan .
Hiroyuki Harada2 Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University , Yushima, Bunkyo-ku, Tokyo, Japan .
Yukinari Kato1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Aoba-ku, Sendai, Miyagi, Japan .

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human epidermal growth factor receptor 2 (HER2) plays a critical role in the progression of breast cancers, and HER2 overexpression is associated with poor clinical outcomes. Trastuzumab is an anti-HER2 humanized antibody that leads to significant survival benefits in patients with HER2-positive metastatic breast cancers. In this study, we developed novel anti-HER2 monoclonal antibodies (mAbs) and characterized their efficacy in flow cytometry, Western blot, and immunohistochemical analyses. Initially, we expressed the full length or ectodomain of HER2 in LN229 glioblastoma cells and then immunized mice with ectodomain of HER2 or LN229/HER2, and performed the first screening by enzyme-linked immunosorbent assays using ectodomain of HER2. Subsequently, we selected mAbs according to their efficacy in flow cytometry (second screening), Western blot (third screening), and immunohistochemical analyses (fourth screening). Among 100 mAb clones, only three mAbs reacted with HER2 in Western blot, and clone H

Indexed as

AnimalsAntibodies, MonoclonalAntibody SpecificityCell Line, TumorCHO CellsCricetulusErb-b2 Receptor Tyrosine KinasesFemaleFlow CytometryHEK293 CellsHumansHybridomasImmunohistochemistryMice, Inbred BALB CProtein BindingSensitivity and SpecificityAntibodies, MonoclonalERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesbreast cancerHER2immunohistochemistrymonoclonal antibody

Identifiers

PMID28700270
PMCPMC6985780

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.