Evidence map›Paper›PMID 40835583›Full record

ArticleACS nano2025

Endogenous Targeting of Lipid Nanoparticles to Kidney Tumors.

Amogh Vaidya, Yun-Chieh Sung, Vanina Toffessi Tcheuyap, Chengcheng Zhang, Ramesh Butti, Arijit Mal, Sean Dilliard, Jing Liu, Eunice Song, Erick Guerrero and 10 more

Abstract read
In one paragraph

Article in ACS nano, 2025. 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
–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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Tissue-specific gene delivery approaches.Bioengineering & translational medicine · 2026
    Review
  6. Review
  7. Nanoparticles in the Treatment of Renal Fibrosis.International journal of nanomedicine · 2026
    Review
  8. Review
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

20 authors.

Amogh VaidyaDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Yun-Chieh SungDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Vanina Toffessi TcheuyapDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.ORCID 0000-0002-6817-9241
Chengcheng ZhangDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Ramesh ButtiDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Arijit MalDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Sean DilliardDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Jing LiuDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Eunice SongDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.ORCID 0000-0003-0642-7083
Erick GuerreroDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Priyanka PatelDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Julien SantelliDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Jeffrey MiyataDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Stephen MooreDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Sumanta ChatterjeeDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Gopinath PrakasamDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.ORCID 0000-0003-1839-7969
Yufen XiaoDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.ORCID 0000-0002-5604-7479
Payal KapurKidney Cancer Program, Simmons Comprehensive Cancer Center, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
James BrugarolasDepartment of Internal Medicine/Hematology-Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Daniel J SiegwartDepartment of Biomedical Engineering, Program in Genetic Drug Engineering, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.ORCID 0000-0003-3823-1931

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Kathryn Ann O'Donnell · 2010 to 2026
$53.7M
University of Texas Southwestern Medical Center SPORE in Kidney CancerP50CA196516 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Payal Kapur, Payal Kapur · 2016 to 2026
$24.7M
Defining the molecular interactions within nanoparticles that enable delivery of long nucleic acidsR01EB025192 · NIBIB · UT SOUTHWESTERN MEDICAL CENTER · PI SIEGWART, DANIEL JOHN · 2018 to 2025
$3.1M
Multiplexed nanoparticle delivery to increase CRISPR/Cas gene editing for enhanced cancer therapyR01CA269787 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Daniel John Siegwart · 2022 to 2026
$1.9M
NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA196516NCI NIH HHS R01 CA269787NIBIB NIH HHS R01 EB025192
6 · The paper itself

Abstract

Although the delivery of genetic therapies to tumors using nanoparticles remains challenging, targeting may be enabled via plasma membrane receptors overexpressed on certain cancer cells. Here, we developed an endogenous targeting strategy for trafficking intravenously administered mRNA (and siRNA) lipid nanoparticles (LNPs) to clear cell renal cell carcinoma (ccRCC) kidney tumors. LNPs were engineered to adsorb circulating plasma vitronectin (Vtn), the ligand for α

Indexed as

Carcinoma, Renal CellKidney NeoplasmsLipidsNanoparticlesAnimalsCell Line, TumorHumansIntegrin alphaVbeta3MiceRNA, MessengerRNA, Small InterferingVitronectinIntegrin alphaVbeta3LipidsRNA, MessengerRNA, Small InterferingVitronectinendogenous targetingHIF2αkidney cancerlipid nanoparticlesmRNARCCsiRNA

Identifiers

PMID40835583
PMCPMC12869457

What OpenQuestion holds

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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.