Evidence map›Paper›PMID 30112821›Full record

ArticleAngewandte Chemie (International ed. in English)2018

Customizable Lipid Nanoparticle Materials for the Delivery of siRNAs and mRNAs.

Owen S Fenton, Kevin J Kauffman, Rebecca L McClellan, James C Kaczmarek, Manhao D Zeng, Jason L Andresen, Luke H Rhym, Michael W Heartlein, Frank DeRosa, Daniel G Anderson

3 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.0field-weighted citation impact, top 8% 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.

NCT05714748 phase1active not recruitingnot on this mapstarted 2023, after this paper: background citation

A Phase I Study of mRNA Vaccine for Patients With EBV-positive Advanced Malignant Tumors

TypeinterventionalSponsorWest China HospitalRan2023 to 2025Enrolled19ConditionsMalignant TumorsArmsEBV mRNA vaccine
NCT05738447 phase1unknown statusnot on this mapstarted 2023, after this paper: background citation

A Phase I Study of mRNA Vaccine for Patients With HBV-positive Advanced Hepatocellular Carcinoma

TypeinterventionalSponsorWest China HospitalRan2023 to 2025Enrolled9ConditionsLiver Cancer, Hepatocellular CarcinomaArmsHBV mRNA vaccine
NCT07004244 phase1recruitingnot on this mapstarted 2025, after this paper: background citation

Safety and Efficacy of KRAS Vaccine in the Treatment of KRAS-mutant Malignancies

TypeinterventionalSponsorSichuan UniversityRan2025 to 2027Enrolled20ConditionsMalignant TumorsArmsKRAS-mutated mRNA vaccine, TORIPALIMAB, Pemetrexed+carboplatin
3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 120 citations in OpenAlex.

  1. Review
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  5. Non-viral gene delivery for non-small cell lung cancer.Annals of translational medicine · 2025
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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

10 authors at 3 institutions in 1 country.

Owen S FentonKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Kevin J KauffmanKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Rebecca L McClellanKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
James C KaczmarekKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Manhao D ZengKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Jason L AndresenKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Luke H RhymKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Michael W HeartleinTranslate Bio, Lexington, MA, 02421, USA.
Frank DeRosaTranslate Bio, Lexington, MA, 02421, USA.
Daniel G AndersonKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.ORCID 0000-0001-5629-4798
Massachusetts Institute of Technology · USTranslate Bio (United States) · USHarvard–MIT Division of Health Sciences and Technology · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
NCI NIH HHS P30 CA014051
6 · The paper itself

Abstract

RNAs are a promising class of therapeutics given their ability to regulate protein concentrations at the cellular level. Developing safe and effective strategies to deliver RNAs remains important for realizing their full clinical potential. Here, we develop lipid nanoparticle formulations that can deliver short interfering RNAs (for gene silencing) or messenger RNAs (for gene upregulation). Specifically, we study how the tail length, tail geometry, and linker spacing in diketopiperazine lipid materials influences LNP potency with siRNAs and mRNAs. Eight lipid materials are synthesized, and 16 total formulations are screened for activity in vitro; the lead material is evaluated with mRNA for in vivo use and demonstrates luciferase protein expression in the spleen. In undertaking this approach, not only do we develop synthetic routes to delivery materials, but we also reveal structural criteria that could be useful for developing next-generation delivery materials for RNA therapeutics.

Indexed as

LipidsNanoparticlesRNA, MessengerRNA, Small InterferingLipidsRNA, MessengerRNA, Small Interferingionizable lipidslipid nanoparticlesmRNAnanomaterialssiRNA

Identifiers

PMID30112821
PMCPMC7548314
OpenAlexW2887151078

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.