Evidence map›Paper›PMID 29700410›Full record

ArticleScientific reports2018

Internalization of CD239 highly expressed in breast cancer cells: a potential antigen for antibody-drug conjugates.

Yamato Kikkawa, Yurie Enomoto-Okawa, Aiko Fujiyama, Takeshi Fukuhara, Nozomi Harashima, Yumika Sugawara, Yoichi Negishi, Fumihiko Katagiri, Kentaro Hozumi, Motoyoshi Nomizu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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
1.1field-weighted citation impact, top 22% 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, 15 citations in OpenAlex.

  1. Trial
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  6. Discovery of antibodies and cognate surface targets for ovarian cancer by surface profiling.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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.

Yamato KikkawaDepartment of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan. kikkawa@toyaku.ac.jp.
Yurie Enomoto-OkawaGraduate School of Science and Engineering, Kagoshima University, Kagoshima, 890-0065, Japan.
Aiko FujiyamaGraduate School of Science and Engineering, Kagoshima University, Kagoshima, 890-0065, Japan.
Takeshi FukuharaLaboratory of Oncology, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Nozomi HarashimaDepartment of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Yumika SugawaraDepartment of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Yoichi NegishiDepartment of Drug Delivery and Molecular Biopharmaceutics, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Fumihiko KatagiriDepartment of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Kentaro HozumiDepartment of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Motoyoshi NomizuDepartment of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Yuji ItoGraduate School of Science and Engineering, Kagoshima University, Kagoshima, 890-0065, Japan.
Tokyo University of Pharmacy and Life Sciences · JPKagoshima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-drug conjugates (ADCs) are attractive in cancer therapy because they can directly bind to cancer cells and provide anticancer activity. To kill cancer cells with ADCs, the target antigens are required not only to be highly and/or selectively expressed on cancer cells but also internalized by the cells. CD239, also known as the Lutheran blood group glycoprotein (Lu) or basal cell adhesion molecule (B-CAM), is a specific receptor for laminin α5, a major component of basement membranes. Here, we show that CD239 is strongly expressed in a subset of breast cancer cells and internalized into the cells. We also produced a human single-chain variable fragment (scFv) specific to CD239 fused with human IgG

Indexed as

EndocytosisAnimalsBiomarkers, TumorBreast NeoplasmsCell Adhesion MoleculesCell Line, TumorCytotoxicity Tests, ImmunologicFemaleHumansImmunoconjugatesImmunoglobulin Fc FragmentsImmunohistochemistryLutheran Blood-Group SystemMiceProtein BindingProtein TransportBCAM protein, humanBiomarkers, TumorCell Adhesion MoleculesImmunoconjugatesImmunoglobulin Fc FragmentsLutheran Blood-Group SystemSingle-Chain Antibodies

Identifiers

PMID29700410
PMCPMC5919910
OpenAlexW2807694289

What OpenQuestion holds

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Registered trials

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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.