Identification of cell cycle-targeting microRNAs through genome-wide screens

By performing nine genome-wide microRNA (miRNA) screens, we recently uncovered a new class of miRNAs, which target multiple cyclins and cyclin-dependent kinases (CDKs). Systemic delivery of selected cell cycle-targeting miRNAs to mouse xenograft models resulted in potent anti-tumorigenic effects wit...

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Main Authors: Bogorad, Roman, Yin, Hao, Anderson, Daniel Griffith
Other Authors: Harvard University--MIT Division of Health Sciences and Technology
Format: Article
Language:English
Published: Informa UK Limited 2019
Subjects:
Online Access:https://hdl.handle.net/1721.1/121999
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author Bogorad, Roman
Yin, Hao
Anderson, Daniel Griffith
author2 Harvard University--MIT Division of Health Sciences and Technology
author_facet Harvard University--MIT Division of Health Sciences and Technology
Bogorad, Roman
Yin, Hao
Anderson, Daniel Griffith
author_sort Bogorad, Roman
collection MIT
description By performing nine genome-wide microRNA (miRNA) screens, we recently uncovered a new class of miRNAs, which target multiple cyclins and cyclin-dependent kinases (CDKs). Systemic delivery of selected cell cycle-targeting miRNAs to mouse xenograft models resulted in potent anti-tumorigenic effects without affecting animals' health. Here, we provide an in-depth description of our miRNA screening methodology, analyses of selected cell cycle-targeting miRNAs, and discuss why miRNA therapy might be a viable therapeutic option for cancer patients.
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spelling mit-1721.1/1219992022-09-29T10:20:15Z Identification of cell cycle-targeting microRNAs through genome-wide screens Bogorad, Roman Yin, Hao Anderson, Daniel Griffith Harvard University--MIT Division of Health Sciences and Technology Koch Institute for Integrative Cancer Research at MIT Developmental Biology Cell Biology Molecular Biology By performing nine genome-wide microRNA (miRNA) screens, we recently uncovered a new class of miRNAs, which target multiple cyclins and cyclin-dependent kinases (CDKs). Systemic delivery of selected cell cycle-targeting miRNAs to mouse xenograft models resulted in potent anti-tumorigenic effects without affecting animals' health. Here, we provide an in-depth description of our miRNA screening methodology, analyses of selected cell cycle-targeting miRNAs, and discuss why miRNA therapy might be a viable therapeutic option for cancer patients. 2019-08-19T13:14:26Z 2019-08-19T13:14:26Z 2017-11-14 2019-08-09T13:22:07Z Article http://purl.org/eprint/type/JournalArticle 1538-4101 1551-4005 https://hdl.handle.net/1721.1/121999 Hydbringa, Per, Yinan Wang, Roman L. Bogorad, Hao Yin, Daniel G. Andersond, Cheng Li, and Piotr Sicinski. "Identification of cell cycle-targeting microRNAs through genome-wide screens." Cell cycle, 16, no. 23 (Nov. 2017): pp. 2241-2248. © 2017 The Author(s) en 10.1080/15384101.2017.1380132 Cell cycle Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Informa UK Limited Taylor & Francis
spellingShingle Developmental Biology
Cell Biology
Molecular Biology
Bogorad, Roman
Yin, Hao
Anderson, Daniel Griffith
Identification of cell cycle-targeting microRNAs through genome-wide screens
title Identification of cell cycle-targeting microRNAs through genome-wide screens
title_full Identification of cell cycle-targeting microRNAs through genome-wide screens
title_fullStr Identification of cell cycle-targeting microRNAs through genome-wide screens
title_full_unstemmed Identification of cell cycle-targeting microRNAs through genome-wide screens
title_short Identification of cell cycle-targeting microRNAs through genome-wide screens
title_sort identification of cell cycle targeting micrornas through genome wide screens
topic Developmental Biology
Cell Biology
Molecular Biology
url https://hdl.handle.net/1721.1/121999
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AT yinhao identificationofcellcycletargetingmicrornasthroughgenomewidescreens
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