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Abstract B38: In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis
In vivo interrogation of the function of genes implicated in tumorigenesis is limited by the need to generate and cross germline mutant mice. Here we describe approaches to model colorectal cancer (CRC) and metastasis that rely on in situ gene editing and orthotopic organoid transplantation in mice...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 2018-05, Vol.78 (10_Supplement), p.B38-B38 |
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creator | Roper, Jatin Tammela, Tuomas Cetinbas, Naniye Malli Akkad, Adam Roghanian, Ali Rickelt, Steffen Almeqdadi, Mohammad Wu, Katherine Oberli, Matthias Sánchez-Rivera, Francisco Park, Yoona Liang, Xu Eng, George Taylor, Martin S. Azimi, Roxana Kedrin, Dmitriy Neupane, Rachit Beyaz, Semir Sicinska, Ewa T. Suarez, Yvelisse Yoo, James Chen, Lillian Zukerberg, Lawrence Katajisto, Pekka Deshpande, Vikram Bass, Adam Tsichlis, Philip N. Lees, Jacqueline Langer, Robert Hynes, Richard O. Chen, Jianzhu Bhutkar, Arjun J. Jacks, Tyler Yilmaz, Ömer H. |
description | In vivo interrogation of the function of genes implicated in tumorigenesis is limited by the need to generate and cross germline mutant mice. Here we describe approaches to model colorectal cancer (CRC) and metastasis that rely on in situ gene editing and orthotopic organoid transplantation in mice without cancer-predisposing mutations. Autochthonous tumor formation is induced by CRISPR/Cas9-based editing of the Apc and Trp53 tumor suppressor genes in colon epithelial cells and by orthotopic transplantation of Apc-edited colon organoids. ApcΔ/Δ;KrasG12D/+;Trp53Δ/Δ (AKP) mouse colon organoids and human CRC organoids engraft in the distal colon and metastasize to the liver. Finally, we apply the orthotopic transplantation model to characterize the clonal dynamics of Lgr5+ stem cells and demonstrate sequential activation of an oncogene in established colon adenomas. These experimental systems enable rapid in vivo characterization of cancer-associated genes and reproduce the entire spectrum of tumor progression and metastasis.
Citation Format: Jatin Roper, Tuomas Tammela, Naniye Malli Cetinbas, Adam Akkad, Ali Roghanian, Steffen Rickelt, Mohammad Almeqdadi, Katherine Wu, Matthias Oberli, Francisco Sánchez-Rivera, Yoona Park, Xu Liang, George Eng, Martin S. Taylor, Roxana Azimi, Dmitriy Kedrin, Rachit Neupane, Semir Beyaz, Ewa T. Sicinska, Yvelisse Suarez, James Yoo, Lillian Chen, Lawrence Zukerberg, Pekka Katajisto, Vikram Deshpande, Adam Bass, Philip N. Tsichlis, Jacqueline Lees, Robert Langer, Richard O. Hynes, Jianzhu Chen, Arjun J. Bhutkar, Tyler Jacks, Ömer H. Yilmaz. In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis [abstract]. In: Proceedings of the AACR Special Conference: Advances in Modeling Cancer in Mice: Technology, Biology, and Beyond; 2017 Sep 24-27; Orlando, Florida. Philadelphia (PA): AACR; Cancer Res 2018;78(10 Suppl):Abstract nr B38. |
doi_str_mv | 10.1158/1538-7445.MOUSEMODELS17-B38 |
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Citation Format: Jatin Roper, Tuomas Tammela, Naniye Malli Cetinbas, Adam Akkad, Ali Roghanian, Steffen Rickelt, Mohammad Almeqdadi, Katherine Wu, Matthias Oberli, Francisco Sánchez-Rivera, Yoona Park, Xu Liang, George Eng, Martin S. Taylor, Roxana Azimi, Dmitriy Kedrin, Rachit Neupane, Semir Beyaz, Ewa T. Sicinska, Yvelisse Suarez, James Yoo, Lillian Chen, Lawrence Zukerberg, Pekka Katajisto, Vikram Deshpande, Adam Bass, Philip N. Tsichlis, Jacqueline Lees, Robert Langer, Richard O. Hynes, Jianzhu Chen, Arjun J. Bhutkar, Tyler Jacks, Ömer H. Yilmaz. In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis [abstract]. In: Proceedings of the AACR Special Conference: Advances in Modeling Cancer in Mice: Technology, Biology, and Beyond; 2017 Sep 24-27; Orlando, Florida. Philadelphia (PA): AACR; Cancer Res 2018;78(10 Suppl):Abstract nr B38.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>DOI: 10.1158/1538-7445.MOUSEMODELS17-B38</identifier><language>eng</language><ispartof>Cancer research (Chicago, Ill.), 2018-05, Vol.78 (10_Supplement), p.B38-B38</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Roper, Jatin</creatorcontrib><creatorcontrib>Tammela, Tuomas</creatorcontrib><creatorcontrib>Cetinbas, Naniye Malli</creatorcontrib><creatorcontrib>Akkad, Adam</creatorcontrib><creatorcontrib>Roghanian, Ali</creatorcontrib><creatorcontrib>Rickelt, Steffen</creatorcontrib><creatorcontrib>Almeqdadi, Mohammad</creatorcontrib><creatorcontrib>Wu, Katherine</creatorcontrib><creatorcontrib>Oberli, Matthias</creatorcontrib><creatorcontrib>Sánchez-Rivera, Francisco</creatorcontrib><creatorcontrib>Park, Yoona</creatorcontrib><creatorcontrib>Liang, Xu</creatorcontrib><creatorcontrib>Eng, George</creatorcontrib><creatorcontrib>Taylor, Martin S.</creatorcontrib><creatorcontrib>Azimi, Roxana</creatorcontrib><creatorcontrib>Kedrin, Dmitriy</creatorcontrib><creatorcontrib>Neupane, Rachit</creatorcontrib><creatorcontrib>Beyaz, Semir</creatorcontrib><creatorcontrib>Sicinska, Ewa T.</creatorcontrib><creatorcontrib>Suarez, Yvelisse</creatorcontrib><creatorcontrib>Yoo, James</creatorcontrib><creatorcontrib>Chen, Lillian</creatorcontrib><creatorcontrib>Zukerberg, Lawrence</creatorcontrib><creatorcontrib>Katajisto, Pekka</creatorcontrib><creatorcontrib>Deshpande, Vikram</creatorcontrib><creatorcontrib>Bass, Adam</creatorcontrib><creatorcontrib>Tsichlis, Philip N.</creatorcontrib><creatorcontrib>Lees, Jacqueline</creatorcontrib><creatorcontrib>Langer, Robert</creatorcontrib><creatorcontrib>Hynes, Richard O.</creatorcontrib><creatorcontrib>Chen, Jianzhu</creatorcontrib><creatorcontrib>Bhutkar, Arjun J.</creatorcontrib><creatorcontrib>Jacks, Tyler</creatorcontrib><creatorcontrib>Yilmaz, Ömer H.</creatorcontrib><title>Abstract B38: In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis</title><title>Cancer research (Chicago, Ill.)</title><description>In vivo interrogation of the function of genes implicated in tumorigenesis is limited by the need to generate and cross germline mutant mice. Here we describe approaches to model colorectal cancer (CRC) and metastasis that rely on in situ gene editing and orthotopic organoid transplantation in mice without cancer-predisposing mutations. Autochthonous tumor formation is induced by CRISPR/Cas9-based editing of the Apc and Trp53 tumor suppressor genes in colon epithelial cells and by orthotopic transplantation of Apc-edited colon organoids. ApcΔ/Δ;KrasG12D/+;Trp53Δ/Δ (AKP) mouse colon organoids and human CRC organoids engraft in the distal colon and metastasize to the liver. Finally, we apply the orthotopic transplantation model to characterize the clonal dynamics of Lgr5+ stem cells and demonstrate sequential activation of an oncogene in established colon adenomas. These experimental systems enable rapid in vivo characterization of cancer-associated genes and reproduce the entire spectrum of tumor progression and metastasis.
Citation Format: Jatin Roper, Tuomas Tammela, Naniye Malli Cetinbas, Adam Akkad, Ali Roghanian, Steffen Rickelt, Mohammad Almeqdadi, Katherine Wu, Matthias Oberli, Francisco Sánchez-Rivera, Yoona Park, Xu Liang, George Eng, Martin S. Taylor, Roxana Azimi, Dmitriy Kedrin, Rachit Neupane, Semir Beyaz, Ewa T. Sicinska, Yvelisse Suarez, James Yoo, Lillian Chen, Lawrence Zukerberg, Pekka Katajisto, Vikram Deshpande, Adam Bass, Philip N. Tsichlis, Jacqueline Lees, Robert Langer, Richard O. Hynes, Jianzhu Chen, Arjun J. Bhutkar, Tyler Jacks, Ömer H. Yilmaz. In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis [abstract]. In: Proceedings of the AACR Special Conference: Advances in Modeling Cancer in Mice: Technology, Biology, and Beyond; 2017 Sep 24-27; Orlando, Florida. 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Here we describe approaches to model colorectal cancer (CRC) and metastasis that rely on in situ gene editing and orthotopic organoid transplantation in mice without cancer-predisposing mutations. Autochthonous tumor formation is induced by CRISPR/Cas9-based editing of the Apc and Trp53 tumor suppressor genes in colon epithelial cells and by orthotopic transplantation of Apc-edited colon organoids. ApcΔ/Δ;KrasG12D/+;Trp53Δ/Δ (AKP) mouse colon organoids and human CRC organoids engraft in the distal colon and metastasize to the liver. Finally, we apply the orthotopic transplantation model to characterize the clonal dynamics of Lgr5+ stem cells and demonstrate sequential activation of an oncogene in established colon adenomas. These experimental systems enable rapid in vivo characterization of cancer-associated genes and reproduce the entire spectrum of tumor progression and metastasis.
Citation Format: Jatin Roper, Tuomas Tammela, Naniye Malli Cetinbas, Adam Akkad, Ali Roghanian, Steffen Rickelt, Mohammad Almeqdadi, Katherine Wu, Matthias Oberli, Francisco Sánchez-Rivera, Yoona Park, Xu Liang, George Eng, Martin S. Taylor, Roxana Azimi, Dmitriy Kedrin, Rachit Neupane, Semir Beyaz, Ewa T. Sicinska, Yvelisse Suarez, James Yoo, Lillian Chen, Lawrence Zukerberg, Pekka Katajisto, Vikram Deshpande, Adam Bass, Philip N. Tsichlis, Jacqueline Lees, Robert Langer, Richard O. Hynes, Jianzhu Chen, Arjun J. Bhutkar, Tyler Jacks, Ömer H. Yilmaz. In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis [abstract]. In: Proceedings of the AACR Special Conference: Advances in Modeling Cancer in Mice: Technology, Biology, and Beyond; 2017 Sep 24-27; Orlando, Florida. Philadelphia (PA): AACR; Cancer Res 2018;78(10 Suppl):Abstract nr B38.</abstract><doi>10.1158/1538-7445.MOUSEMODELS17-B38</doi></addata></record> |
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title | Abstract B38: In vivo genome editing and organoid transplantation models of colorectal cancer and metastasis |
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