All Stories

  1. ERK5 is activated by oncogenic BRAF and promotes melanoma growth
  2. Targeting chronic myeloid leukemia stem cells with the hypoxia-inducible factor inhibitor acriflavine
  3. The Leukemic Stem Cell Niche: Adaptation to “Hypoxia” versus Oncogene Addiction
  4. Low-dose methotrexate enhances cycling of highly anaplastic cancer cells
  5. Different BCR/Abl protein suppression patterns as a converging trait of Chronic Myeloid Leukemia cell adaptation to energy restriction
  6. Fibronectin induces macrophage migration through a SFK-FAK/CSF-1R pathway
  7. Crosstalk between MAPK and HH_GLI signaling in cancer
  8. The complex metabolic network gearing the G1/S transition in leukemic stem cells: Hints to a rational use of antineoplastic agents
  9. PGE2 synergizes with CSF-1R
  10. Hypoxia up-regulates SERPINB3 through HIF-2α in human liver cancer cells
  11. Positive correlation of HIF2α and SERPINB3 in human hepatocellular carcinoma: selectivity and prognostic implications
  12. Colony-Stimulating Factor-1 Receptor in the Polarization of Macrophages: A Target for Turning Bad to Good Ones?
  13. Lipid rafts: integrated platforms for vascular organization offering therapeutic opportunities
  14. The metabolically-modulated stem cell niche: a dynamic scenario regulating cancer cell phenotype and resistance to therapy
  15. The mitogen-activated protein kinase ERK5 regulates the development and growth of hepatocellular carcinoma
  16. 786: The mitogen-activated protein kinase ERK5 regulates the development and growth of hepatocellular carcinoma
  17. Possible mechanisms and function of nuclear trafficking of the colony-stimulating factor-1 receptor
  18. One more stem cell niche: how the sensitivity of chronic myeloid leukemia cells to imatinib mesylate is modulated within a "hypoxic" environment
  19. Chromatin-associated CSF-1R binds to the promoter of proliferation-related genes in breast cancer cells
  20. Correction to Barbetti V, et al. Epigenetics Volume 8, Issue 2; pp. 210–9
  21. Hypoxia-resistant profile implies vulnerability of cancer stem cells to physiological agents, which suggests new therapeutic targets
  22. The Culture-Repopulating Ability Assays and Incubation in Low Oxygen: A Simple Way to Test Drugs on Leukaemia Stem or Progenitor Cells
  23. AML1/ETO sensitizes via TRAIL acute myeloid leukemia cells to the pro-apoptotic effects of hypoxia
  24. Time- and residue-specific differences in histone acetylation induced by VPA and SAHA in AML1/ETO-positive leukemia cells
  25. The involvement of a Nanog, Klf4 and c-Myc transcriptional circuitry in the intertwining between neoplastic progression and reprogramming
  26. The Colony-Stimulating Factor-1 (CSF-1) Receptor Sustains ERK1/2 Activation and Proliferation in Breast Cancer Cell Lines
  27. Hypoxia Selects Bortezomib-Resistant Stem Cells of Chronic Myeloid Leukemia
  28. Glucose availability in hypoxia regulates the selection of chronic myeloid leukemia progenitor subsets with different resistance to imatinib-mesylate
  29. Correction: Granulocyte Maturation after Butyrate Treatment of Leukemic Blasts
  30. p38 and cancer: Yang gets yin
  31. ERK5/BMK1 Is Indispensable for Optimal Colony-Stimulating Factor 1 (CSF-1)-Induced Proliferation in Macrophages in a Src-Dependent Fashion
  32. ERK5 differentially regulates PDGF-induced proliferation and migration of hepatic stellate cells
  33. Selective anti-leukaemic activity of low-dose histone deacetylase inhibitor ITF2357 on AML1/ETO-positive cells
  34. Severe Hypoxia Defines Heterogeneity and Selects Highly Immature Progenitors Within Clonal Erythroleukemia Cells
  35. The c-Jun-N-terminal-Kinase inhibitor SP600125 enhances the butyrate derivative D1-induced apoptosis via caspase 8 activation in Kasumi 1 t(8;21) acute myeloid leukaemia cells
  36. Hypoxia suppresses BCR/Abl and selects imatinib-insensitive progenitors within clonal CML populations
  37. 332 Activation of ERK5, a member of the mapk family, differentially regulates proliferation and migration of hepatic stellate cells
  38. Focal adhesion kinase is redistributed to focal complexes and mediates cell spreading in macrophages in response to M-CSF
  39. Corrections
  40. Tryptophan availability selectively limits NO-synthase induction in macrophages
  41. Low M r Phosphotyrosine Protein Phosphatase Associates and Dephosphorylates p125 Focal Adhesion Kinase, Interfering with Cell Motility and Spreading
  42. Opposite effects of different doses of MCSF on ERK phosphorylation and cell proliferation in macrophages
  43. Transmodulation of Cell Surface Regulatory Molecules via Ectodomain Shedding
  44. TNF- -Converting Enzyme Cleaves the Macrophage Colony-Stimulating Factor Receptor in Macrophages Undergoing Activation
  45. The expansion of murine bone marrow cells preincubated in hypoxia as an in vitro indicator of their marrow-repopulating ability
  46. Incubation of murine bone marrow cells in hypoxia ensures the maintenance of marrow-repopulating ability together with the expansion of committed progenitors
  47. Low M r phosphotyrosine protein phosphatase activity on fibroblast growth factor receptor is not associated with enzyme translocation
  48. The Low-Molecular-Weight Phosphotyrosine Protein Phosphatase, when Overexpressed, Reduces the Mitogenic Response to Macrophage Colony-Stimulating Factor and Tyrosine Phosphorylation of Its Receptor
  49. INTERLEUKIN 2 DOWN-MODULATES THE MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR IN MURINE MACROPHAGES