Sheila Thomas, Ph.D.
| Title | Director of Diversity and Minority Affairs |
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| Institution | Harvard Medical School |
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| Department | Division Of Medical Sciences |
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| Address | Harvard Graduate School of Arts & Sci Holyoke Ctr 350 1350 Massachusetts Ave Cambridge MA 02138
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| Phone | 617/495-5315 |
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| Title | Assistant Professor of Medicine |
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| Institution | Beth Israel Deaconess Medical Center |
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| Department | Medicine |
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| Division | Hematology/Oncology |
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Overview The major interests of my laboratory are in the area of Cancer Cell Biology. In particular, we are interested in elucidating and understanding signaling networks which control key cellular processes. Over the past several years, we have focused on understanding pathways regulating cell migration in normal and malignant cells. We have used both in vivo and in vitro models to elucidate the functions of specific cytoskeletal scaffolding proteins in development and to define the mechanisms by which they regulate processes such as cell migration and transformation. Our work has provided a number of key in vivo and in vitro models for the field (Liu et al., 1999; Hagel et al., 2002; Webb et al., 2004; Chen et al., 2005). These tools have been critical for understanding the molecular basis by which one of these proteins regulates cell migration. Through this work, we have also identified unexpected roles for some of these proteins in a process called autophagy (Chen et al., 2008). Autophagy is a highly conserved mechanism for controlling cellular homeostasis. Misregulation of this process has been implicated in numerous human pathogenic states including heart disease, cancer, and neurodegenerative disorders. In addition, a number of viral and bacterial pathogens hijack the autophagy machinery. Our goal is to identify the regulatory networks controlling autophagy and to determine how misregulation of this pathway contributes to human disease
Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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Mack HI, Zheng B, Asara J, Thomas SM. AMPK-dependent phosphorylation of ULK1 regulates ATG9 localization. Autophagy. 2012 Aug; 8(8):1197-214.
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Armour SM, Baur JA, Hsieh SN, Land-Bracha A, Thomas SM, Sinclair DA. Inhibition of mammalian S6 kinase by resveratrol suppresses autophagy. Aging (Albany NY). 2009 Jun; 1(6):515-28.
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Chen GC, Lee JY, Tang HW, Debnath J, Thomas SM, Settleman J. Genetic interactions between Drosophila melanogaster Atg1 and paxillin reveal a role for paxillin in autophagosome formation. Autophagy. 2008 Jan; 4(1):37-45.
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Yang L, Kowalski JR, Yacono P, Bajmoczi M, Shaw SK, Froio RM, Golan DE, Thomas SM, Luscinskas FW. Endothelial cell cortactin coordinates intercellular adhesion molecule-1 clustering and actin cytoskeleton remodeling during polymorphonuclear leukocyte adhesion and transmigration. J Immunol. 2006 Nov 1; 177(9):6440-9.
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Yang W, Klaman LD, Chen B, Araki T, Harada H, Thomas SM, George EL, Neel BG. An Shp2/SFK/Ras/Erk signaling pathway controls trophoblast stem cell survival. Dev Cell. 2006 Mar; 10(3):317-27.
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Yang L, Kowalski JR, Zhan X, Thomas SM, Luscinskas FW. Endothelial cell cortactin phosphorylation by Src contributes to polymorphonuclear leukocyte transmigration in vitro. Circ Res. 2006 Feb 17; 98(3):394-402.
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Brachmann SM, Yballe CM, Innocenti M, Deane JA, Fruman DA, Thomas SM, Cantley LC. Role of phosphoinositide 3-kinase regulatory isoforms in development and actin rearrangement. Mol Cell Biol. 2005 Apr; 25(7):2593-606.
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Chen GC, Turano B, Ruest PJ, Hagel M, Settleman J, Thomas SM. Regulation of Rho and Rac signaling to the actin cytoskeleton by paxillin during Drosophila development. Mol Cell Biol. 2005 Feb; 25(3):979-87.
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Kowalski JR, Egile C, Gil S, Snapper SB, Li R, Thomas SM. Cortactin regulates cell migration through activation of N-WASP. J Cell Sci. 2005 Jan 1; 118(Pt 1):79-87.
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Webb DJ, Donais K, Whitmore LA, Thomas SM, Turner CE, Parsons JT, Horwitz AF. FAK-Src signalling through paxillin, ERK and MLCK regulates adhesion disassembly. Nat Cell Biol. 2004 Feb; 6(2):154-61.
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Didier C, Broday L, Bhoumik A, Israeli S, Takahashi S, Nakayama K, Thomas SM, Turner CE, Henderson S, Sabe H, Ronai Z. RNF5, a RING finger protein that regulates cell motility by targeting paxillin ubiquitination and altered localization. Mol Cell Biol. 2003 Aug; 23(15):5331-45.
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Carneiro AM, Ingram SL, Beaulieu JM, Sweeney A, Amara SG, Thomas SM, Caron MG, Torres GE. The multiple LIM domain-containing adaptor protein Hic-5 synaptically colocalizes and interacts with the dopamine transporter. J Neurosci. 2002 Aug 15; 22(16):7045-54.
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Hagel M, George EL, Kim A, Tamimi R, Opitz SL, Turner CE, Imamoto A, Thomas SM. The adaptor protein paxillin is essential for normal development in the mouse and is a critical transducer of fibronectin signaling. Mol Cell Biol. 2002 Feb; 22(3):901-15.
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Liu ZX, Yu CF, Nickel C, Thomas S, Cantley LG. Hepatocyte growth factor induces ERK-dependent paxillin phosphorylation and regulates paxillin-focal adhesion kinase association. J Biol Chem. 2002 Mar 22; 277(12):10452-8.
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