Evidence map›Paper›PMID 35425350›Full record

ArticleRSC advances2022

Homogeneous antibody-angiopep 2 conjugates for effective brain targeting.

Yasuaki Anami, Wei Xiong, Aiko Yamaguchi, Chisato M Yamazaki, Ningyan Zhang, Zhiqiang An, Kyoji Tsuchikama

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. A patent review of cyclin-dependent kinase 5 (CDK5) inhibitors (1999-2025).Frontiers in bioengineering and biotechnology · 2026
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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

7 authors at 1 institution in 1 country.

Yasuaki AnamiTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.ORCID https://orcid.org/0000-0001-5136-7708
Wei XiongTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.
Aiko YamaguchiTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.ORCID https://orcid.org/0000-0002-7631-3164
Chisato M YamazakiTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.ORCID https://orcid.org/0000-0002-0785-7352
Ningyan ZhangTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.ORCID https://orcid.org/0000-0002-4348-2180
Zhiqiang AnTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.ORCID https://orcid.org/0000-0001-9309-2335
Kyoji TsuchikamaTexas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, The University of Texas Health Center at Houston Houston Texas 77054 USA Kyoji.Tsuchikama@uth.tmc.edu Zhiqiang.An@uth.tmc.edu Ningyan.Zhang@uth.tmc.edu Chisato.Tsuchikama@uth.tmc.edu Aiko.Yamaguchi@uth.tmc.edu.ORCID https://orcid.org/0000-0002-2359-0408
Brown Foundation · US

Funding

Chemical approaches for generating blood-brain barrier-permeable antibody conjugatesR35GM138264 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TSUCHIKAMA, KYOJI · 2020 to 2024
$1.9M
NIGMS NIH HHS R35 GM138264
6 · The paper itself

Abstract

Antibody-based therapy has shown great success in the treatment of many diseases, including cancers. While antibodies and antibody-drug conjugates (ADCs) have also been evaluated for central nervous system (CNS) disorders as well as brain tumors, their therapeutic efficacy can be substantially limited due to low permeability across the blood-brain barrier (BBB). Thus, improving BBB permeability of therapeutic antibodies is critical in establishing this drug class as a reliable clinical option for CNS diseases. Here, we report that, compared with a conventional heterogeneous conjugation, homogeneous conjugation of the synthetic BBB shuttle peptide angiopep-2 (Ang2) to a monoclonal antibody (mAb) provides improved binding affinity for brain microvascular endothelial cells

Identifiers

PMID35425350
PMCPMC8979263
OpenAlexW4210568310

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.