Evidence map›Paper›PMID 32182186›Full record

ArticleMonoclonal antibodies in immunodiagnosis and immunotherapy2020

Antibody-Drug Conjugates Using Mouse-Canine Chimeric Anti-Dog Podoplanin Antibody Exerts Antitumor Activity in a Mouse Xenograft Model.

Yukinari Kato, Yuji Ito, Tomokazu Ohishi, Manabu Kawada, Takuro Nakamura, Yusuke Sayama, Masato Sano, Teizo Asano, Miyuki Yanaka, Saki Okamoto and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Monoclonal antibodies in immunodiagnosis and immunotherapy, 2020. 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 27% 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, 13 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

14 authors at 3 institutions in 1 country.

Yukinari KatoDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yuji ItoDepartment of Chemistry and Bioscience, Graduate School of Science and Engineering, Kagoshima University, Kagoshima, Japan.
Tomokazu OhishiInstitute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, Shizuoka, Japan.
Manabu KawadaInstitute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, Shizuoka, Japan.
Takuro NakamuraDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yusuke SayamaDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Masato SanoDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Teizo AsanoDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Miyuki YanakaDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Saki OkamotoDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Saori HandaDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yu KomatsuDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Junko TakeiDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Mika K KanekoDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tohoku University · JPMicrobial Chemistry Research Foundation · JPKagoshima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-drug conjugates (ADCs), which consist of a monoclonal antibody (mAb), a linker, and a payload, can deliver a drug to cancer tissues. We previously produced an anti-dog podoplanin (dPDPN) mAb, PMab-38, which reacts with dPDPN-expressing canine melanomas and squamous cell carcinomas (SCCs), but not with dPDPN-expressing canine type I alveolar cells or lymphatic endothelial cells, indicating that PMab-38 possesses cancer specificity. In this study, we developed an ADC, P38B-DM1, using the mouse-canine chimeric anti-dPDPN antibody, P38B as the antibody, a peptide linker, and emtansine as the payload using the chemical conjugation by affinity peptide (CCAP) method. We investigated its cytotoxicity against dPDPN-overexpressed Chinese hamster ovary (CHO/dPDPN) cells

Indexed as

AnimalsAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityCarcinoma, Squamous CellCell Line, TumorCHO CellsCricetinaeCricetulusDog DiseasesDogsEndothelial CellsHeterograftsHumansImmunoconjugatesMelanomaMembrane GlycoproteinsAntibodies, MonoclonalImmunoconjugatesMembrane GlycoproteinsPDPN protein, humanPodoplaninantibody–drug conjugatedog podoplaninmonoclonal antibody

Identifiers

PMID32182186
PMCPMC7185362
OpenAlexW3011229924

What OpenQuestion holds

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LicenceCC BY
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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.