Cited 6 time in
An Antibody-CRISPR/Cas Conjugate Platform for Target-Specific Delivery and Gene Editing in Cancer
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Yang, Seungju | - |
| dc.contributor.author | Im, San Hae | - |
| dc.contributor.author | Chung, Ju Yeon | - |
| dc.contributor.author | Lee, Juhee | - |
| dc.contributor.author | Lee, Kyung-Hun | - |
| dc.contributor.author | Kang, Yoo Kyung | - |
| dc.contributor.author | Chung, Hyun Jung | - |
| dc.date.accessioned | 2024-04-12T02:30:31Z | - |
| dc.date.available | 2024-04-12T02:30:31Z | - |
| dc.date.issued | 2024-06 | - |
| dc.identifier.issn | 2198-3844 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/70221 | - |
| dc.description.abstract | The CRISPR/Cas system has been introduced as an innovative tool for therapy, however achieving specific delivery to the target has been a major challenge. Here, an antibody-CRISPR/Cas conjugate platform that enables specific delivery and target gene editing in HER2-positive cancer is introduced. The CRISPR/Cas system by replacing specific residues of Cas9 with an unnatural amino acid is engineered, that can be complexed with a nanocarrier and bioorthogonally functionalized with a monoclonal antibody targeting HER2. The resultant antibody-conjugated CRISPR/Cas nanocomplexes can be specifically delivered and induce gene editing in HER2-positive cancer cells in vitro. It is demonstrated that the in vivo delivery of the antibody-CRISPR/Cas nanocomplexes can effectively disrupt the plk1 gene in HER2-positive ovarian cancer, resulting in substantial suppression of tumor growth. The current study presents a useful therapeutic platform for antibody-mediated delivery of CRISPR/Cas for the treatment of various cancers and genetic diseases. Here, an antibody-CRISPR/Cas conjugate platform that enables specific delivery and target gene editing in HER2-positive cancer is introduced. It is demonstrated that the in vivo delivery of the antibody-CRISPR/Cas nanocomplexes can effectively disrupt the plk1 gene in HER2-positive ovarian cancer, resulting in substantial suppression of tumor growth. image | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Wiley-VCH Verlag | - |
| dc.title | An Antibody-CRISPR/Cas Conjugate Platform for Target-Specific Delivery and Gene Editing in Cancer | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1002/advs.202308763 | - |
| dc.identifier.scopusid | 2-s2.0-85188915069 | - |
| dc.identifier.wosid | 001193245900001 | - |
| dc.identifier.bibliographicCitation | Advanced Science, v.11, no.21 | - |
| dc.citation.title | Advanced Science | - |
| dc.citation.volume | 11 | - |
| dc.citation.number | 21 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordAuthor | antibody conjugation | - |
| dc.subject.keywordAuthor | cancer therapy | - |
| dc.subject.keywordAuthor | CRISPR/Cas | - |
| dc.subject.keywordAuthor | in vivo gene editing | - |
| dc.subject.keywordAuthor | specific delivery | - |
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