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Kwon, Taejoon
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Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9

Author(s)
Kwon, TaejoonRa, Jae SunLee, SoyoungBaek, In-JoonKhim, Keon WooLee, Eun ASong, Eun KyungOtarbayev, DaniyarJung, WoojaePark, Yong HwanWie, MinwooBae, JuyoungCheng, HimchanPark, Jun HongKim, NamwooSeo, YuriYun, SeongminKim, Ha EunMoon, Hyo EunPaek, Sun HaPark, Tae JooPark, Young UnRhee, HwanseokChoi, Jang HyunCho, Seung WooMyung, Kyungjae
Issued Date
2022-03
DOI
10.1073/pnas.2103532119
URI
https://scholarworks.unist.ac.kr/handle/201301/57307
Fulltext
https://www.pnas.org/content/119/9/e2103532119
Citation
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.119, no.9, pp.e2103532119
Abstract
An ideal cancer therapeutic strategy involves the selective killing of cancer cells without affecting the surrounding normal cells. However, researchers have failed to develop such methods for achieving selective cancer cell death because of shared features between cancerous and normal cells. In this study, we have developed a therapeutic strategy called the cancer-specific insertions–deletions (InDels) attacker (CINDELA) to selectively induce cancer cell death using the CRISPR-Cas system. CINDELA utilizes a previously unexplored idea of introducing CRISPR-mediated DNA double-strand breaks (DSBs) in a cancer-specific fashion to facilitate specific cell death. In particular, CINDELA targets multiple InDels with CRISPR-Cas9 to produce many DNA DSBs that result in cancer-specific cell death. As a proof of concept, we demonstrate here that CINDELA selectively kills human cancer cell lines, xenograft human tumors in mice, patient-derived glioblastoma, and lung patient-driven xenograft tumors without affecting healthy human cells or altering mouse growth.
Publisher
NATL ACAD SCIENCES
ISSN
0027-8424
Keyword (Author)
CRISPRinsertiondeletioncancerdouble-strand breaks
Keyword
GENOME-WIDEDNA-REPAIRINHIBITIONSEQUENCEINSERTION

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