Evidence map›Paper›PMID 38214504›Full record

ArticleMolecular pharmaceutics2024

Kai Jin, You-Cheng Liao, Tzu-Chun Cheng, Xin Li, Wen-Jui Lee, Fengmei Pi, Daniel Jasinski, Li-Ching Chen, Mitch A Phelps, Yuan-Soon Ho and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2024. 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
2.1field-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, 10 citations in OpenAlex.

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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 3 institutions in 2 countries.

Kai JinDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.
You-Cheng LiaoGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110031, Taiwan.
Tzu-Chun ChengInstitute of Biochemistry and Molecular Biology, China Medical University, Taichung 406040, Taiwan.
Xin LiDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.
Wen-Jui LeeDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.
Fengmei PiDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.
Daniel JasinskiDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.
Li-Ching ChenDepartment of Biological Science and Technology, China Medical University, Taichung 406040, Taiwan.
Mitch A PhelpsDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.
Yuan-Soon HoInstitute of Biochemistry and Molecular Biology, China Medical University, Taichung 406040, Taiwan.
Peixuan GuoDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.ORCID 0000-0001-5706-2833
The Ohio State University · USChina Medical University · TWTaipei Medical University · TW

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
Optimizing RNA nanoparticles size and shape for enhancing cancer targeting and treatmentU01CA207946 · NCI · OHIO STATE UNIVERSITY · PI CARSON, WILLIAM E., GUO, PEIXUAN · 2016 to 2020
$2.7M
RNA Nanosystem for Posterior Eye Drug DeliveryR01EY031452 · NEI · UNIVERSITY OF CINCINNATI · PI LI, KEVIN S. · 2021 to 2024
$1.6M
NCI NIH HHS P30 CA016058NCI NIH HHS U01 CA207946NEI NIH HHS R01 EY031452
6 · The paper itself

Abstract

RNA therapeutics has advanced into the third milestone in pharmaceutical drug development, following chemical and protein therapeutics. RNA itself can serve as therapeutics, carriers, regulators, or substrates in drug development. Due to RNA's motile, dynamic, and deformable properties, RNA nanoparticles have demonstrated spontaneous targeting and accumulation in cancer vasculature and fast excretion through the kidney glomerulus to urine to prevent possible interactions with healthy organs. Furthermore, the negatively charged phosphate backbone of RNA results in general repulsion from negatively charged lipid cell membranes for further avoidance of vital organs. Thus, RNA nanoparticles can spontaneously enrich tumor vasculature and efficiently enter tumor cells via specific targeting, while those not entering the tumor tissue will clear from the body quickly. These favorable parameters have led to the expectation that RNA has low or little toxicity. RNA nanoparticles have been well characterized for their anticancer efficacy; however, little detail on RNA nanoparticle pathology and safety is known. Here, we report the

Indexed as

NanoparticlesNeoplasmsAnimalsDrug Delivery SystemsHumansPyrimidinesRNA, Small InterferingPyrimidinesRNA, Small InterferingCMC productionpRNA 3WJpRNA 4WJRNA immune responseRNA nanotechnologyRNA pathologyRNA Safety

Identifiers

PMID38214504
PMCPMC10976369
OpenAlexW4390794955

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.