Evidence map›Paper›PMID 37485817›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Bioorthogonal CRISPR/Cas9-Drug Conjugate: A Combinatorial Nanomedicine Platform.

Marcel Janis Beha, Joo-Chan Kim, San Hae Im, Yunsu Kim, Seungju Yang, Juhee Lee, Yu Ri Nam, Haeshin Lee, Hee-Sung Park, Hyun Jung Chung

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Bioorthogonal CRISPR/Cas9-Drug Conjugate: A Combinatorial Nanomedicine Platform.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
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 1 institution in 1 country.

Marcel Janis BehaDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Joo-Chan KimDepartment of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
San Hae ImDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Yunsu KimDepartment of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Seungju YangDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Juhee LeeDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Yu Ri NamDepartment of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Haeshin LeeDepartment of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Hee-Sung ParkDepartment of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.
Hyun Jung ChungDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Republic of Korea.ORCID 0000-0001-5055-902X
Korea Advanced Institute of Science and Technology · KR

Funding

Ministry of Health and Welfare HI22C2010National Research Foundation of Korea 2021M3E5E3080383National Research Foundation of Korea 2021R1A2C2011763National Research Foundation of Korea 2022R1A4A5028131National Research Foundation of Korea 2023R1A2C1005945Samsung Science and Technology Foundation SSTF-BA1702-09
6 · The paper itself

Abstract

Bioconjugation of proteins can substantially expand the opportunities in biopharmaceutical development, however, applications are limited for the gene editing machinery despite its tremendous therapeutic potential. Here, a self-delivered nanomedicine platform based on bioorthogonal CRISPR/Cas9 conjugates, which can be armed with a chemotherapeutic drug for combinatorial therapy is introduced. It is demonstrated that multi-functionalized Cas9 with a drug and polymer can form self-condensed nanocomplexes, and induce significant gene editing upon delivery while avoiding the use of a conventional carrier formulation. It is shown that the nanomedicine platform can be applied for combinatorial therapy by incorporating the anti-cancer drug olaparib and targeting the RAD52 gene, leading to significant anti-tumor effects in BRCA-mutant cancer. The current development provides a versatile nanomedicine platform for combination treatment of human diseases such as cancer.

Indexed as

CRISPR-Cas SystemsGene Transfer TechniquesGene EditingHumansNanomedicinePharmaceutical PreparationsPharmaceutical Preparationsbioorthogonalcancer therapychemotherapeutic drugscombinatorial deliveryCRISPR/Cas9gene editingnanomedicinesunnatural amino acids

Identifiers

PMID37485817
PMCPMC10520654
OpenAlexW4385186531

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.