Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids

The relative contribution of fallopian tube (FT) or ovarian surface epithelium (OSE) to high-grade serous ovarian cancer (HG-SOC) development is unclear. Here, the authors establish organoid models from murine oviductal and OSE tissues that allow cancer modeling via CRISPR-Cas9 genome editing, and r...

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Autores principales: Kadi Lõhmussaar, Oded Kopper, Jeroen Korving, Harry Begthel, Celien P. H. Vreuls, Johan H. van Es, Hans Clevers
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/b561dc387d334f75b89e8a94ccc8b593
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spelling oai:doaj.org-article:b561dc387d334f75b89e8a94ccc8b5932021-12-02T15:49:49ZAssessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids10.1038/s41467-020-16432-02041-1723https://doaj.org/article/b561dc387d334f75b89e8a94ccc8b5932020-05-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-16432-0https://doaj.org/toc/2041-1723The relative contribution of fallopian tube (FT) or ovarian surface epithelium (OSE) to high-grade serous ovarian cancer (HG-SOC) development is unclear. Here, the authors establish organoid models from murine oviductal and OSE tissues that allow cancer modeling via CRISPR-Cas9 genome editing, and report a dual origin of murine HG-SOC.Kadi LõhmussaarOded KopperJeroen KorvingHarry BegthelCelien P. H. VreulsJohan H. van EsHans CleversNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Kadi Lõhmussaar
Oded Kopper
Jeroen Korving
Harry Begthel
Celien P. H. Vreuls
Johan H. van Es
Hans Clevers
Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids
description The relative contribution of fallopian tube (FT) or ovarian surface epithelium (OSE) to high-grade serous ovarian cancer (HG-SOC) development is unclear. Here, the authors establish organoid models from murine oviductal and OSE tissues that allow cancer modeling via CRISPR-Cas9 genome editing, and report a dual origin of murine HG-SOC.
format article
author Kadi Lõhmussaar
Oded Kopper
Jeroen Korving
Harry Begthel
Celien P. H. Vreuls
Johan H. van Es
Hans Clevers
author_facet Kadi Lõhmussaar
Oded Kopper
Jeroen Korving
Harry Begthel
Celien P. H. Vreuls
Johan H. van Es
Hans Clevers
author_sort Kadi Lõhmussaar
title Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids
title_short Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids
title_full Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids
title_fullStr Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids
title_full_unstemmed Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids
title_sort assessing the origin of high-grade serous ovarian cancer using crispr-modification of mouse organoids
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/b561dc387d334f75b89e8a94ccc8b593
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AT odedkopper assessingtheoriginofhighgradeserousovariancancerusingcrisprmodificationofmouseorganoids
AT jeroenkorving assessingtheoriginofhighgradeserousovariancancerusingcrisprmodificationofmouseorganoids
AT harrybegthel assessingtheoriginofhighgradeserousovariancancerusingcrisprmodificationofmouseorganoids
AT celienphvreuls assessingtheoriginofhighgradeserousovariancancerusingcrisprmodificationofmouseorganoids
AT johanhvanes assessingtheoriginofhighgradeserousovariancancerusingcrisprmodificationofmouseorganoids
AT hansclevers assessingtheoriginofhighgradeserousovariancancerusingcrisprmodificationofmouseorganoids
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