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Sheila Thomas, Ph.D.

TitleDirector of Diversity and Minority Affairs
InstitutionHarvard Medical School
DepartmentDivision Of Medical Sciences
AddressHarvard Graduate School of Arts & Sci
Holyoke Ctr 350
1350 Massachusetts Ave
Cambridge MA 02138
Phone617/495-5315
Other Positions
TitleAssistant Professor of Medicine
InstitutionBeth Israel Deaconess Medical Center
DepartmentMedicine
DivisionHematology/Oncology


 Overview 
 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 
 selected publications
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Mack HI, Zheng B, Asara J, Thomas SM. AMPK-dependent phosphorylation of ULK1 regulates ATG9 localization. Autophagy. 2012 Aug; 8(8):1197-214.
    View in: PubMed
  2. 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.
    View in: PubMed
  3. 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.
    View in: PubMed
  4. 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.
    View in: PubMed
  5. 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.
    View in: PubMed
  6. 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.
    View in: PubMed
  7. 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.
    View in: PubMed
  8. 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.
    View in: PubMed
  9. 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.
    View in: PubMed
  10. 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.
    View in: PubMed
  11. 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.
    View in: PubMed
  12. 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.
    View in: PubMed
  13. 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.
    View in: PubMed
  14. 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.
    View in: PubMed
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