Evidence map›Paper›PMID 42006041›Full record

ArticleAdvanced functional materials2026

RNA-Micelles as Self-Assembling Structures for Efficient Co-Delivery of Synergistic siRNA and Nucleoside Analogues to Treat CRC Lung Metastasis.

Kai Jin, Piotr Rychahou, Daniel W Binzel, B Mark Evers, Peixuan Guo

Abstract read
In one paragraph

Article in Advanced functional materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Kai JinDivision of Pharmaceutics and Pharmacology, College of Pharmacy, Center for RNA Nanobiotechnology and Nanomedicine, Comprehensive Cancer Center, College of Medicine, The Ohio State University, Columbus, Ohio, USA.
Piotr RychahouMarkey Cancer Center, Department of Surgery, University of Kentucky, Lexington, Kentucky, USA.
Daniel W BinzelDivision of Pharmaceutics and Pharmacology, College of Pharmacy, Center for RNA Nanobiotechnology and Nanomedicine, Comprehensive Cancer Center, College of Medicine, The Ohio State University, Columbus, Ohio, USA.
B Mark EversMarkey Cancer Center, Department of Surgery, University of Kentucky, Lexington, Kentucky, USA.
Peixuan GuoDivision of Pharmaceutics and Pharmacology, College of Pharmacy, Center for RNA Nanobiotechnology and Nanomedicine, Comprehensive Cancer Center, College of Medicine, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0001-5706-2833

Funding

Mechanism and approach to inactivate mutant KRAS of lung metastatic colon cancer by RNA-ligand-displaying exosome to co-deliver dCas9--gRNA ribonucleoprotein complex and KRAS siRNAR01CA293945 · NCI · OHIO STATE UNIVERSITY · PI BIN GUO, PEIXUAN GUO · 2024 to 2026
$2.4M
RNA Nanosystem for Posterior Eye Drug DeliveryR01EY031452 · NEI · UNIVERSITY OF CINCINNATI · PI LI, KEVIN S. · 2021 to 2024
$1.6M
NCI NIH HHS R01 CA293945NEI NIH HHS R01 EY031452
6 · The paper itself

Abstract

SiRNA has been widely studied in cancer gene silencing over the last 25 years. However, few siRNA-based therapeutics have been approved by the FDA. An RNA-micelle platform provides a powerful therapeutic tool through simple one-step, high-yield production that is capable of efficient colorectal cancer lung metastasis treatment, a current lethal condition with a short survival rate post-diagnosis. Here, it is reported that the use of RNA-micelles co-carrying siRNA and nucleoside analogues to completely inhibit lung metastasis of colorectal cancer (CRC). The major advantage of the RNA-micelle is the successful co-delivery of siRNA and chemotherapeutic agent in a single delivery vehicle while specifically targeting CRC cells via incorporation of an oncogenic surface receptor ligand. It was found that RNA-micelles could combine to silence survivin protein expression via siRNA delivery, which in turn increased the efficacy of the delivered chemotherapeutic agent. Both siRNA and high-payload nucleoside-analogues were incorporated onto a single micelle, which remained stable during in vivo circulation, rather than individual RNA nanoparticles, thus generating this advantageous synergistic cancer regression. This platform provides a powerful therapeutic tool to address colorectal cancer lung metastasis, a currently serious, lethal disease that has a very poor prognosis following diagnosis.

Indexed as

colorectal cancer lung metastasisdrug deliverygemcitabineRNA-micelleRNA nanobiotechnologysiRNAspecific delivery

Identifiers

PMID42006041
PMCPMC13089865

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.