Mark A Labarge

Summary

Affiliation: Lawrence Berkeley National Laboratory
Country: USA

Publications

  1. pmc Of microenvironments and mammary stem cells
    Mark A Labarge
    Lawrence Berkeley National Laboratory, Berkeley, CA, USA
    Stem Cell Rev 3:137-46. 2007
  2. pmc Is CD133 a marker of metastatic colon cancer stem cells?
    Mark A Labarge
    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA
    J Clin Invest 118:2021-4. 2008
  3. pmc Context, tissue plasticity, and cancer: are tumor stem cells also regulated by the microenvironment?
    Mina J Bissell
    Department Cancer Biology, Life Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720, USA
    Cancer Cell 7:17-23. 2005
  4. ncbi request reprint Molecular deconstruction, detection, and computational prediction of microenvironment-modulated cellular responses to cancer therapeutics
    Mark A Labarge
    Life Science Division of Lawrence Berkeley National Laboratory, University of California, 1 Cylcotron Rd, MS977, Berkeley, CA 94720, USA Electronic address
    Adv Drug Deliv Rev 69:123-31. 2014
  5. ncbi request reprint Breaking the canon: indirect regulation of Wnt signaling in mammary stem cells by MMP3
    Mark A Labarge
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
    Cell Stem Cell 13:259-60. 2013
  6. pmc Aging phenotypes in cultured normal human mammary epithelial cells are correlated with decreased telomerase activity independent of telomere length
    Klara Sputova
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
    Genome Integr 4:4. 2013
  7. pmc The difficulty of targeting cancer stem cell niches
    Mark A Labarge
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
    Clin Cancer Res 16:3121-9. 2010
  8. pmc Human mammary progenitor cell fate decisions are products of interactions with combinatorial microenvironments
    Mark A Labarge
    Lawrence Berkeley National Laboratory, Division of Life Sciences, Berkeley, CA 94720, USA
    Integr Biol (Camb) 1:70-9. 2009
  9. pmc Accumulation of multipotent progenitors with a basal differentiation bias during aging of human mammary epithelia
    James C Garbe
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA
    Cancer Res 72:3687-701. 2012
  10. ncbi request reprint Age-related dysfunction in mechanotransduction impairs differentiation of human mammary epithelial progenitors
    Fanny A Pelissier
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA Center for Cancer Biomarkers, Department of Biomedicine, University of Bergen, Bergen 5009, Norway
    Cell Rep 7:1926-39. 2014

Collaborators

Detail Information

Publications15

  1. pmc Of microenvironments and mammary stem cells
    Mark A Labarge
    Lawrence Berkeley National Laboratory, Berkeley, CA, USA
    Stem Cell Rev 3:137-46. 2007
    ..These studies together create a robust portrait of mammary gland biology and identify the location of the stem cell niche, elucidate a developmental hierarchy, and suggest how the niche might be manipulated for therapeutic benefit...
  2. pmc Is CD133 a marker of metastatic colon cancer stem cells?
    Mark A Labarge
    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA
    J Clin Invest 118:2021-4. 2008
    ..In light of these new findings, the popular notion that CD133 is a marker of colon CSCs may need to be revised...
  3. pmc Context, tissue plasticity, and cancer: are tumor stem cells also regulated by the microenvironment?
    Mina J Bissell
    Department Cancer Biology, Life Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720, USA
    Cancer Cell 7:17-23. 2005
  4. ncbi request reprint Molecular deconstruction, detection, and computational prediction of microenvironment-modulated cellular responses to cancer therapeutics
    Mark A Labarge
    Life Science Division of Lawrence Berkeley National Laboratory, University of California, 1 Cylcotron Rd, MS977, Berkeley, CA 94720, USA Electronic address
    Adv Drug Deliv Rev 69:123-31. 2014
    ..Ultimately we propose that a merger of these technologies will enable more accurate pre-clinical drug discovery. ..
  5. ncbi request reprint Breaking the canon: indirect regulation of Wnt signaling in mammary stem cells by MMP3
    Mark A Labarge
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
    Cell Stem Cell 13:259-60. 2013
    ..2013) now show that MMP3, independent of its proteolytic activity, regulates murine mammary stem cells by sequestering noncanonical Wnt signaling ligands, which has implications for breast cancer pathogenesis. ..
  6. pmc Aging phenotypes in cultured normal human mammary epithelial cells are correlated with decreased telomerase activity independent of telomere length
    Klara Sputova
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
    Genome Integr 4:4. 2013
    ....
  7. pmc The difficulty of targeting cancer stem cell niches
    Mark A Labarge
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
    Clin Cancer Res 16:3121-9. 2010
    ....
  8. pmc Human mammary progenitor cell fate decisions are products of interactions with combinatorial microenvironments
    Mark A Labarge
    Lawrence Berkeley National Laboratory, Division of Life Sciences, Berkeley, CA 94720, USA
    Integr Biol (Camb) 1:70-9. 2009
    ..We report on the functional ability of those proteins of the mammary gland that maintain quiescence, maintain the progenitor state, and guide progenitor differentiation towards myoepithelial and luminal lineages...
  9. pmc Accumulation of multipotent progenitors with a basal differentiation bias during aging of human mammary epithelia
    James C Garbe
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA
    Cancer Res 72:3687-701. 2012
    ..Together, our findings provide a cellular basis to explain the observed vulnerability to breast cancer that increases with age...
  10. ncbi request reprint Age-related dysfunction in mechanotransduction impairs differentiation of human mammary epithelial progenitors
    Fanny A Pelissier
    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA Center for Cancer Biomarkers, Department of Biomedicine, University of Bergen, Bergen 5009, Norway
    Cell Rep 7:1926-39. 2014
    ..Thus, aging phenotypes of mammary epithelia may arise partly because alterations in Hippo pathway activation impair microenvironment-directed differentiation and lineage specificity. ..
  11. pmc Programmed cell-to-cell variability in Ras activity triggers emergent behaviors during mammary epithelial morphogenesis
    Jennifer S Liu
    Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA 94158, USA
    Cell Rep 2:1461-70. 2012
    ..Our results directly demonstrate that cell-to-cell variability in pathway activation within local populations of epithelial cells can drive emergent behaviors during epithelial morphogenesis...
  12. pmc Evidence for a stem cell hierarchy in the adult human breast
    Rene Villadsen
    Department of Cellular and Molecular Medicine, Faculty of Health Sciences, and Zoophysiological Laboratory, University of Copenhagen, and Department of Pathology, State University Hospital, Copenhagen, Denmark
    J Cell Biol 177:87-101. 2007
    ..These findings identify an adult human breast ductal stem cell activity and its earliest descendants...
  13. pmc IGF-I increases bone marrow contribution to adult skeletal muscle and enhances the fusion of myelomonocytic precursors
    Alessandra Sacco
    Department of Molecular Pharmacology, Baxter Laboratory in Genetic Pharmacology, Stanford University School of Medicine, Stanford, CA 94305, USA
    J Cell Biol 171:483-92. 2005
    ..These results provide novel evidence that a single factor, IGF-I, is sufficient to enhance the fusion of bone marrow derivatives with adult skeletal muscle...
  14. pmc Hematopoietic contribution to skeletal muscle regeneration by myelomonocytic precursors
    Regis Doyonnas
    Baxter Laboratory in Genetic Pharmacology and Department of Molecular Pharmacology, Stanford University School of Medicine, 269 Campus Drive, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 101:13507-12. 2004
    ..Irrespective of the underlying mechanisms, these data suggest that the HSC derivatives that integrate into regenerating muscle fibers exist in the pool of hematopoietic cells known as myelomonocytic progenitors...
  15. ncbi request reprint Biological progression from adult bone marrow to mononucleate muscle stem cell to multinucleate muscle fiber in response to injury
    Mark A Labarge
    Baxter Laboratory for Genetic Pharmacology, Department of Microbiology and Immunology, Department of Molecular Pharmacology, Stanford University School of Medicine, CCSR 4215, Stanford, CA 94305, USA
    Cell 111:589-601. 2002
    ..The stress-induced progression of BMDC to muscle satellite cell to muscle fiber results in a contribution to as many as 3.5% of muscle fibers and is due to developmental plasticity in response to environmental cues...