Evidence map›Paper›PMID 38145661›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2024

Enabling safer, more potent oligonucleotide therapeutics with bottlebrush polymer conjugates.

Peiru Chen, Yun Wei, Tingyu Sun, Jiachen Lin, Ke Zhang

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2024. 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
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 13 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

5 authors at 1 institution in 1 country.

Peiru ChenDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA.
Yun WeiDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA.
Tingyu SunDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA.
Jiachen LinDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA.
Ke ZhangDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA; Department of Chemical Engineering and Bioengineering, Northeastern University, Boston, MA 02115, USA. Electronic address: k.zhang@northeastern.edu.
Northeastern University · US

Funding

Making Oligonucleotides Better Biopharmaceuticals by Steric ProtectionR01GM121612 · NIGMS · NORTHEASTERN UNIVERSITY · PI Ke Zhang · 2017 to 2026
$3.7M
Molecular brush-conjugated antisense oligonucleotide as a pan-KRAS depletion agentR42CA275425 · NCI · PACDNA LLC · PI ZHANG, KE · 2022 to 2024
$2.5M
Targeting Oncogenic KRAS with Brush-Architectured Poly(ethylene glycol)-DNA ConjugatesR01CA251730 · NCI · NORTHEASTERN UNIVERSITY · PI ZHANG, KE · 2020 to 2024
$1.9M
NCI NIH HHS R01 CA251730NCI NIH HHS R42 CA275425NIGMS NIH HHS R01 GM121612
6 · The paper itself

Abstract

Oligonucleotide therapeutics have the unique ability to address traditionally undruggable targets through various target engagement pathways. However, despite advances in chemically modified oligonucleotides and carrier-assisted delivery systems such as lipid nanoparticles and protein/peptide conjugates, the development of oligonucleotide drugs is still plagued with lackluster potency, narrow therapeutic window, poor delivery to non-liver target sites, and/or high potential for toxicity and unwanted immune system activation. In this perspective, we discuss an unconventional delivery solution based upon bottlebrush polymers, which overcomes many key challenges in oligonucleotide drug development. We address the molecular basis of the polymer's ability to enhance tissue bioavailability and drug potency, reduce side effects, and suppress anti-carrier immunity. Furthermore, we discuss the potential of the technology in advancing oligonucleotide-based therapies for non-liver targets.

Indexed as

Drug DevelopmentOligonucleotidesBiological AvailabilityPolymersTechnologyOligonucleotidesPolymersDrug deliveryGene regulationOligonucleotide

Identifiers

PMID38145661
PMCPMC10922259
OpenAlexW4390242429

What OpenQuestion 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 OpenQuestion graph.