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Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9
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 thi...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892319/ https://www.ncbi.nlm.nih.gov/pubmed/35217600 http://dx.doi.org/10.1073/pnas.2103532119 |
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author | Kwon, Taejoon Ra, Jae Sun Lee, Soyoung Baek, In-Joon Khim, Keon Woo Lee, Eun A Song, Eun Kyung Otarbayev, Daniyar Jung, Woojae Park, Yong Hwan Wie, Minwoo Bae, Juyoung Cheng, Himchan Park, Jun Hong Kim, Namwoo Seo, Yuri Yun, Seongmin Kim, Ha Eun Moon, Hyo Eun Paek, Sun Ha Park, Tae Joo Park, Young Un Rhee, Hwanseok Choi, Jang Hyun Cho, Seung Woo Myung, Kyungjae |
author_facet | Kwon, Taejoon Ra, Jae Sun Lee, Soyoung Baek, In-Joon Khim, Keon Woo Lee, Eun A Song, Eun Kyung Otarbayev, Daniyar Jung, Woojae Park, Yong Hwan Wie, Minwoo Bae, Juyoung Cheng, Himchan Park, Jun Hong Kim, Namwoo Seo, Yuri Yun, Seongmin Kim, Ha Eun Moon, Hyo Eun Paek, Sun Ha Park, Tae Joo Park, Young Un Rhee, Hwanseok Choi, Jang Hyun Cho, Seung Woo Myung, Kyungjae |
author_sort | Kwon, Taejoon |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8892319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-88923192022-08-25 Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 Kwon, Taejoon Ra, Jae Sun Lee, Soyoung Baek, In-Joon Khim, Keon Woo Lee, Eun A Song, Eun Kyung Otarbayev, Daniyar Jung, Woojae Park, Yong Hwan Wie, Minwoo Bae, Juyoung Cheng, Himchan Park, Jun Hong Kim, Namwoo Seo, Yuri Yun, Seongmin Kim, Ha Eun Moon, Hyo Eun Paek, Sun Ha Park, Tae Joo Park, Young Un Rhee, Hwanseok Choi, Jang Hyun Cho, Seung Woo Myung, Kyungjae Proc Natl Acad Sci U S A Biological Sciences 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. National Academy of Sciences 2022-02-25 2022-03-01 /pmc/articles/PMC8892319/ /pubmed/35217600 http://dx.doi.org/10.1073/pnas.2103532119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Kwon, Taejoon Ra, Jae Sun Lee, Soyoung Baek, In-Joon Khim, Keon Woo Lee, Eun A Song, Eun Kyung Otarbayev, Daniyar Jung, Woojae Park, Yong Hwan Wie, Minwoo Bae, Juyoung Cheng, Himchan Park, Jun Hong Kim, Namwoo Seo, Yuri Yun, Seongmin Kim, Ha Eun Moon, Hyo Eun Paek, Sun Ha Park, Tae Joo Park, Young Un Rhee, Hwanseok Choi, Jang Hyun Cho, Seung Woo Myung, Kyungjae Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 |
title | Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 |
title_full | Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 |
title_fullStr | Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 |
title_full_unstemmed | Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 |
title_short | Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9 |
title_sort | precision targeting tumor cells using cancer-specific indel mutations with crispr-cas9 |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892319/ https://www.ncbi.nlm.nih.gov/pubmed/35217600 http://dx.doi.org/10.1073/pnas.2103532119 |
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