Literature DB >> 21466894

Mouse models of myelodysplastic syndromes.

Joanna Wegrzyn1, Jeffrey C Lam, Aly Karsan.   

Abstract

Myelodysplastic syndromes (MDS) are hematopoietic malignancies characterized by peripheral cytopenias in the face of normo- or hypercellular, dysplastic bone marrow that arise from mutations in the hematopoietic stem/progenitor cell (HSPC). The disease is characterized by multiple cytogenetic and molecular defects, which result in an extremely heterogeneous phenotype. Recently, significant efforts have been made to develop appropriate mouse models to study this complex disease. Because of the heterogeneity of MDS, no single model is able to capture the MDS phenotype in its entirety. In this review, we describe several MDS mouse models and discuss the advances made in our understanding of the different disease mechanisms within the malignant clone and the marrow microenvironment. In addition, we describe progress in xenotransplantation models of MDS and discuss questions that remain to be answered.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21466894     DOI: 10.1016/j.leukres.2011.03.007

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  11 in total

Review 1.  Revisiting the case for genetically engineered mouse models in human myelodysplastic syndrome research.

Authors:  Ting Zhou; Marsha C Kinney; Linda M Scott; Sandra S Zinkel; Vivienne I Rebel
Journal:  Blood       Date:  2015-06-15       Impact factor: 22.113

2.  Mito-protective autophagy is impaired in erythroid cells of aged mtDNA-mutator mice.

Authors:  XiuJie Li-Harms; Sandra Milasta; John Lynch; Christopher Wright; Aashish Joshi; Rekha Iyengar; Geoffrey Neale; Xi Wang; Yong-Dong Wang; Tomas A Prolla; James E Thompson; Joseph T Opferman; Douglas R Green; John Schuetz; Mondira Kundu
Journal:  Blood       Date:  2014-11-19       Impact factor: 22.113

3.  Growth factor independence 1 (Gfi1) regulates cell-fate decision of a bipotential granulocytic-monocytic precursor defined by expression of Gfi1 and CD48.

Authors:  Lothar Vassen; Ulrich Dührsen; Christian Kosan; Hui Zeng; Tarik Möröy
Journal:  Am J Blood Res       Date:  2012-11-25

Review 4.  Engineering mouse models with myelodysplastic syndrome human candidate genes; how relevant are they?

Authors:  Stephanie Beurlet; Christine Chomienne; Rose Ann Padua
Journal:  Haematologica       Date:  2012-10-12       Impact factor: 9.941

5.  The orphan nuclear receptor EAR-2 (NR2F6) inhibits hematopoietic cell differentiation and induces myeloid dysplasia in vivo.

Authors:  Christine V Ichim; Dzana D Dervovic; Lap Shu Alan Chan; Claire J Robertson; Alden Chesney; Marciano D Reis; Richard A Wells
Journal:  Biomark Res       Date:  2018-12-07

6.  AQP0 is a novel surface marker for deciphering abnormal erythropoiesis.

Authors:  Tso-Fu Wang; Guan-Ling Lin; Sung-Chao Chu; Chang-Chin Chen; Yu-Shan Liou; Hsin-Hou Chang; Der-Shan Sun
Journal:  Stem Cell Res Ther       Date:  2021-05-06       Impact factor: 6.832

7.  Novel spontaneous myelodysplastic syndrome mouse model.

Authors:  Weisha Li; Lin Cao; Mengyuan Li; Xingjiu Yang; Wenlong Zhang; Zhiqi Song; Xinpei Wang; Lingyan Zhang; Grant Morahan; Chuan Qin; Ran Gao
Journal:  Animal Model Exp Med       Date:  2021-05-14

8.  Splicing factor 3b subunit 1 (Sf3b1) haploinsufficient mice display features of low risk Myelodysplastic syndromes with ring sideroblasts.

Authors:  Valeria Visconte; Ali Tabarroki; Li Zhang; Yvonne Parker; Edy Hasrouni; Reda Mahfouz; Kyoichi Isono; Haruhiko Koseki; Mikkael A Sekeres; Yogen Saunthararajah; John Barnard; Daniel Lindner; Heesun J Rogers; Ramon V Tiu
Journal:  J Hematol Oncol       Date:  2014-12-07       Impact factor: 17.388

9.  Alkylator-Induced and Patient-Derived Xenograft Mouse Models of Therapy-Related Myeloid Neoplasms Model Clinical Disease and Suggest the Presence of Multiple Cell Subpopulations with Leukemia Stem Cell Activity.

Authors:  Brian A Jonas; Carl Johnson; Dita Gratzinger; Ravindra Majeti
Journal:  PLoS One       Date:  2016-07-18       Impact factor: 3.240

10.  Oxidative stress-induced JNK/AP-1 signaling is a major pathway involved in selective apoptosis of myelodysplastic syndrome cells by Withaferin-A.

Authors:  Karine Z Oben; Sara S Alhakeem; Mary K McKenna; Jason A Brandon; Rajeswaran Mani; Sunil K Noothi; Liu Jinpeng; Shailaja Akunuru; Sanjit K Dhar; Inder P Singh; Ying Liang; Chi Wang; Ahmed Abdel-Latif; Harold F Stills; Daret K St Clair; Hartmut Geiger; Natarajan Muthusamy; Kaoru Tohyama; Ramesh C Gupta; Subbarao Bondada
Journal:  Oncotarget       Date:  2017-08-24
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