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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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.
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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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