Evidence map›Paper›PMID 39984637›Full record

ArticleNature nanotechnology2025

Systemic HER3 ligand-mimicking nanobioparticles enter the brain and reduce intracranial tumour growth.

Felix Alonso-Valenteen, Simoun Mikhael, HongQiang Wang, Jessica Sims, Michael Taguiam, James Teh, Sam Sances, Michelle Wong, Tianxin Miao, Dustin Srinivas and 13 more

Abstract read
In one paragraph

Article in Nature nanotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

23 authors.

Felix Alonso-ValenteenDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Simoun MikhaelDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
HongQiang WangNeurosurgical Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Jessica SimsDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Michael TaguiamDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
James TehDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Sam SancesBoard of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Michelle WongDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Tianxin MiaoDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Dustin SrinivasDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Nelyda Gonzalez-AlmeydaDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Ryan H ChoDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Romny SanchezCalifornia State University, Northridge, CA, USA.
Kimngan NguyenleDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Erik SerranoDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Briana OndatjeBoard of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Rebecca L BenhaghnazarDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Harry B GrayCalifornia Institute of Technology, Pasadena, CA, USA.
Zeev GrossTechnion-Israel Institute, Haifa, Israel.
John YuNeurosurgical Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Clive N SvendsenDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Ravinder AbrolDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Lali K Medina-KauweDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA. MedinaL@cshs.org.ORCID http://orcid.org/0000-0002-9807-5523

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
Effects of opioids on reward systems in organ chipsUG3NS105703 · NINDS · CEDARS-SINAI MEDICAL CENTER · PI SVENDSEN, CLIVE NIELS · 2017 to 2020
$5.2M
Targeting inhibitor-resistant breast tumors with HER3-homing nano-capsidsR01CA258204 · NCI · CEDARS-SINAI MEDICAL CENTER · PI LALI K MEDINA-KAUWE · 2022 to 2026
$1.9M
Nucleocapsid bioparticles eliciting multi-pronged attack on tumor metastasesR01CA270324 · NCI · CEDARS-SINAI MEDICAL CENTER · PI LALI K MEDINA-KAUWE · 2022 to 2026
$1.5M
Multidisciplinary Pulmonary Research Training ProgramT32HL134637 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI NOBLE, PAUL WESLEY · 2017 to 2021
$1.3M
NCATS NIH HHS UL1 TR001881NCI NIH HHS R01 CA258204NCI NIH HHS R01 CA270324NHLBI NIH HHS T32 HL134637NINDS NIH HHS UG3 NS105703U.S. Department of Defense (United States Department of Defense) W81XWH-15-1-0604U.S. Department of Defense (United States Department of Defense) W81XWH1910592U.S. Department of Defense (United States Department of Defense) W81XWH-22-1-0953U.S. Department of Health & Human Services | National Institutes of Health (NIH) UG3NS105703
6 · The paper itself

Abstract

Crossing the blood-brain barrier (BBB) and reaching intracranial tumours is a clinical challenge for current targeted interventions including antibody-based therapies, contributing to poor patient outcomes. Increased cell surface density of human epidermal growth factor receptor 3 (HER3) is associated with a growing number of metastatic tumour types and is observed on tumour cells that acquire resistance to a growing number of clinical targeted therapies. Here we describe the evaluation of HER3-homing nanobiological particles (nanobioparticles (NBPs)) on such tumours in preclinical models and our discovery that systemic NBPs could be found in the brain even in the absence of such tumours. Our subsequent studies described here show that HER3 is prominently associated with both mouse and human brain endothelium and with extravasation of systemic NBPs in mice and in human-derived BBB chips in contrast to non-targeted agents. In mice, systemically delivered NBPs carrying tumoricidal agents reduced the growth of intracranial triple-negative breast cancer cells, which also express HER3, with improved therapeutic profile compared to current therapies and compared to agents using traditional BBB transport routes. As HER3 associates with a growing number of metastatic tumours, the NBPs described here may offer targeted efficacy especially when such tumours localize to the brain.

Indexed as

Antineoplastic AgentsBrainBrain NeoplasmsNanoparticlesReceptor, ErbB-3Triple Negative Breast NeoplasmsAnimalsBlood-Brain BarrierCell Line, TumorFemaleHumansLigandsMiceAntineoplastic AgentsERBB3 protein, humanLigandsReceptor, ErbB-3

Identifiers

PMID39984637
PMCPMC12095042

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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.