L
Lisheng Wang
Researcher at Ohio State University
Publications - 6
Citations - 845
Lisheng Wang is an academic researcher from Ohio State University. The author has contributed to research in topics: Myeloid leukemia & Retinoblastoma protein. The author has an hindex of 4, co-authored 6 publications receiving 803 citations.
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Journal ArticleDOI
Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutated nucleophosmin
Ramiro Garzon,Michela Garofalo,Maria Paola Martelli,Roger Briesewitz,Lisheng Wang,Cecilia Fernandez-Cymering,Stefano Volinia,Chang Gong Liu,Susanne Schnittger,Torsten Haferlach,Arcangelo Liso,Daniela Diverio,Marco Mancini,Giovanna Meloni,Robin Foà,Massimo F. Martelli,Cristina Mecucci,Carlo M. Croce,Brunangelo Falini +18 more
TL;DR: A unique miRNA signature is identified that distinguishes NPMc+ mutated from the cytoplasmic-negative (NPM1 unmutated) cases and includes the up-regulation of miR-10a, miR -10b, several let-7 and miR –29 family members and support a role for miRNAs in the regulation of HOX genes in this leukemia subtype.
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Novel c-CBL and CBL-b ubiquitin ligase mutations in human acute myeloid leukemia
Michael A. Caligiuri,Roger Briesewitz,Jianhua Yu,Lisheng Wang,Min Wei,Kristy J. Arnoczky,Trent B. Marburger,Jing Wen,Danilo Perrotti,Clara D. Bloomfield,Susan P. Whitman +10 more
TL;DR: Novel mutations in c-CBL and CBL-b have been identified in human AML and may represent potential targets for novel therapeutics.
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Pharmacologic inhibition of CDK4/6: mechanistic evidence for selective activity or acquired resistance in acute myeloid leukemia
Lisheng Wang,Jie Wang,Bradley W. Blaser,Anne Marie Duchemin,Donna Frances Kusewitt,Tom Liu,Michael A. Caligiuri,Roger Briesewitz +7 more
TL;DR: CDK4/6 can be a therapeutic target in Flt3 ITD AML but also in primary Flt 3 wt AML, and acquired resistance to CDK 4/6 inhibition can arise through activation CDK2.
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Creating Diverse Target-Binding Surfaces on FKBP12: Synthesis and Evaluation of a Rapamycin Analogue Library
Xianghong Wu,Lisheng Wang,Yaohua Han,Nicholas Regan,Pui-Kai Li,Miguel A. Villalona,Xiche Hu,Roger Briesewitz,Dehua Pei +8 more
TL;DR: Results show that FKBP12 binds to most of the rapalogs with high affinity (K(I) values in the nanomolar to low micromolar range), creating a large repertoire of composite surfaces for potential recognition of macromolecular targets such as proteins.
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Essential Role of the INK4/CDK4,6/Rb/E2F Signaling Pathway in AML with the Flt3 Internal Tandem Duplication.
TL;DR: The data suggest that the activation of the INK4/CDK4,6/Rb/E2F pathway by Flt3 ITD has an essential role for proliferation and survival in AML cells, and PD-0332991 was neither cytotoxic nor cytostatic in THP-1 and U937 cells.