Evidence map›Paper›PMID 30548114›Full record

ArticleCancer science2019

Anti-tumor effects of mAb against L-type amino acid transporter 1 (LAT1) bound to human and monkey LAT1 with dual avidity modes.

Shiho Ueda, Hidemi Hayashi, Takako Miyamoto, Shinya Abe, Kana Hirai, Kanji Matsukura, Hideki Yagi, Yuta Hara, Kinji Yoshida, Shogo Okazaki and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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  18. Heteromeric Solute Carriers: Function, Structure, Pathology and Pharmacology.Advances in experimental medicine and biology · 2021
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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

16 authors at 6 institutions in 2 countries.

Shiho UedaCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Hidemi HayashiLink Genomics, Inc., Tokyo, Japan.
Takako MiyamotoCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Shinya AbeLaboratory of Biological Protection, Institute for Viral Research, Kyoto University, Kyoto, Japan.
Kana HiraiCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Kanji MatsukuraCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Hideki YagiSchool of Pharmacy, International University of Health and Welfare, Otawara, Japan.
Yuta HaraCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Kinji YoshidaCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Shogo OkazakiDivision of Development and Aging, Research Institute for Biomedical Sciences, Tokyo University of Science, Chiba, Japan.
Masakazu TamuraModality Research Laboratories, Biologics Division, Daiichi Sankyo Co., Ltd, Tokyo, Japan.
Yuki AbeBiologics & Immuno-Oncology Laboratories, R&D Division, Daiichi Sankyo Co., Ltd, Tokyo, Japan.
Toshinori AgatsumaBiologics & Immuno-Oncology Laboratories, R&D Division, Daiichi Sankyo Co., Ltd, Tokyo, Japan.
Shin-Ichiro NiwaLink Genomics, Inc., Tokyo, Japan.
Kazue MasukoCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.
Takashi MasukoCell Biology Laboratory, School of Pharmacy, Kindai University, Osaka, Japan.ORCID 0000-0002-2410-2007
Kindai University · JPDaiichi-Sankyo (Japan) · JPID Genomics (United States) · USInternational University of Health and Welfare · JPKyoto University · JPTokyo University of Science · JP

Funding

"Academic Frontier" Project F000132 (2005-2007)Japan Science and Technology Agency Sports, Science and Technology-supported Program for the Strategic Research Foundation at Private Universities S1411037 (2014-2018)MEXT (Ministry of Education, Culture, the "Adaptable and Seamless Technology Transfer Program through R&D" Project AS2115048G (2009-2001)
6 · The paper itself

Abstract

L-Type amino acid transporter 1 (LAT1) disulfide linked to CD98 heavy chain (hc) is highly expressed in most cancer cells, but weakly expressed in normal cells. In the present study, we developed novel anti-LAT1 mAbs and showed internalization activity, inhibitory effects of amino acid uptake and cell growth and antibody-dependent cellular cytotoxicity, as well as in vivo antitumor effects in athymic mice. Furthermore, we examined the reactivity of mAbs with LAT1 of Macaca fascicularis to evaluate possible side-effects of antihuman LAT1 mAbs in clinical trials. Antihuman LAT1 mAbs reacted with ACHN human and MK.P3 macaca kidney-derived cells, and this reactivity was significantly decreased by siRNAs against LAT1. Macaca LAT1 cDNA was cloned from MK.P3, and only two amino acid differences between human and macaca LAT1 were seen. RH7777 rat hepatoma and HEK293 human embryonic kidney cells expressing macaca LAT1 were established as stable transfectants, and antihuman LAT1 mAbs were equivalently reactive against transfectants expressing human or macaca LAT1. Dual (high and low) avidity modes were detected in transfectants expressing macaca LAT1, MK.P3, ACHN and HCT116 human colon cancer cells, and K

Indexed as

A549 CellsAmino AcidsAnimalsAntibodies, MonoclonalCell LineCell Line, TumorCell ProliferationHaplorhiniHCT116 CellsHEK293 CellsHeLa CellsHumansLarge Neutral Amino Acid-Transporter 1Macaca fascicularisMiceMice, NudeAmino AcidsAntibodies, MonoclonalLarge Neutral Amino Acid-Transporter 1antitumor effectavidityLAT1monoclonal antibodynon-human primate

Identifiers

PMID30548114
PMCPMC6361610
OpenAlexW2904684213

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.