Literature DB >> 20632859

Induced pluripotent stem cells: opportunities as research and development tools in 21st century drug discovery.

Rebecca K Rowntree1, John D McNeish.   

Abstract

Pluripotent embryonic stem cells (ESCs), when compared with transformed, primary or engineered cells, have unique characteristics and advantages that have resulted in the development of important cell-based tools in modern drug discovery. However, a key limitation has been the availability of human ESCs from patients with specific medical needs and the broad range of genetic variation represented worldwide. Induced pluripotent stem (iPS) cells are derived from somatic cells that are reprogrammed to a pluripotent stem cell state and have functional characteristics similar to ESCs. The demonstration that human iPS cells can be derived, with relative ease, through the introduction of transcription factor combinations has allowed the generation of disease-specific iPS cell lines. Therefore, iPS cell technology may deliver robust, human pluripotent cell lines from a wide range of clinical phenotypes and genotypes. Although human iPS cell technology is still a new tool in drug discovery, the promise that this technology will impact the discovery of new therapies can be projected based on the uptake of stem cell applications in biopharmaceutical sciences. Here, the near-term opportunities that iPS cells may deliver to drug discoverers to generate and test hypotheses will be discussed, with a focus on the specific strengths and weaknesses of iPS cell technology. Finally, the future perspective will address novel opportunities iPS cells could uniquely deliver to the preclinical development of new drug therapies.

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Year:  2010        PMID: 20632859     DOI: 10.2217/rme.10.36

Source DB:  PubMed          Journal:  Regen Med        ISSN: 1746-0751            Impact factor:   3.806


  12 in total

Review 1.  Present state and future perspectives of using pluripotent stem cells in toxicology research.

Authors:  Anna M Wobus; Peter Löser
Journal:  Arch Toxicol       Date:  2011-01-12       Impact factor: 5.153

Review 2.  Stem cells as cellular vehicles for gene therapy against glioblastoma.

Authors:  Wei Wang; Fanlong Liu; Bingyu Xiang; Charlie Xiang; Xiaozhou Mou
Journal:  Int J Clin Exp Med       Date:  2015-10-15

Review 3.  The Use of Induced Pluripotent Stem Cells for the Study and Treatment of Liver Diseases.

Authors:  Marc C Hansel; Julio C Davila; Massoud Vosough; Roberto Gramignoli; Kristen J Skvorak; Kenneth Dorko; Fabio Marongiu; William Blake; Stephen C Strom
Journal:  Curr Protoc Toxicol       Date:  2016-02-01

4.  Drug development in pediatric psychiatry: current status, future trends.

Authors:  John S March; Joerg M Fegert
Journal:  Child Adolesc Psychiatry Ment Health       Date:  2012-02-07       Impact factor: 3.033

5.  Stem cells in drug screening for neurodegenerative disease.

Authors:  Hyun-Jung Kim; Chang Yun Jin
Journal:  Korean J Physiol Pharmacol       Date:  2012-02-28       Impact factor: 2.016

Review 6.  Building a microphysiological skin model from induced pluripotent stem cells.

Authors:  Zongyou Guo; Claire A Higgins; Brian M Gillette; Munenari Itoh; Noriko Umegaki; Karl Gledhill; Samuel K Sia; Angela M Christiano
Journal:  Stem Cell Res Ther       Date:  2013-12-20       Impact factor: 6.832

7.  DMSO efficiently down regulates pluripotency genes in human embryonic stem cells during definitive endoderm derivation and increases the proficiency of hepatic differentiation.

Authors:  Katherine Czysz; Stephen Minger; Nick Thomas
Journal:  PLoS One       Date:  2015-02-06       Impact factor: 3.240

8.  Induced Pluripotent Stem Cells for Disease Modeling and Evaluation of Therapeutics for Niemann-Pick Disease Type A.

Authors:  Yan Long; Miao Xu; Rong Li; Sheng Dai; Jeanette Beers; Guokai Chen; Ferri Soheilian; Ulrich Baxa; Mengqiao Wang; Juan J Marugan; Silvia Muro; Zhiyuan Li; Roscoe Brady; Wei Zheng
Journal:  Stem Cells Transl Med       Date:  2016-08-02       Impact factor: 6.940

9.  Induction of reprogramming of human amniotic epithelial cells into iPS cells by overexpression of Yap, Oct4, and Sox2 through the activation of the Hippo-Yap pathway.

Authors:  Yanhui Zhao; Xinfeng Fei; Jianming Guo; Gang Zou; Weidong Pan; Jingju Zhang; Yongyi Huang; Te Liu; Weiwei Cheng
Journal:  Exp Ther Med       Date:  2017-05-24       Impact factor: 2.447

10.  Neural stem cells for disease modeling and evaluation of therapeutics for infantile (CLN1/PPT1) and late infantile (CLN2/TPP1) neuronal ceroid lipofuscinoses.

Authors:  Ni Sima; Rong Li; Wei Huang; Miao Xu; Jeanette Beers; Jizhong Zou; Steven Titus; Elizabeth A Ottinger; Juan J Marugan; Xing Xie; Wei Zheng
Journal:  Orphanet J Rare Dis       Date:  2018-04-10       Impact factor: 4.303

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