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      Primary myelofibrosis and its targeted therapy.

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          Abstract

          Primary myelofibrosis is a unique entity among BCR-ABL-negative myeloproliferative diseases, manifesting as bone marrow fibrosis and pancytopenia. Considerable evidence indicates that genetic and epigenetic abnormalities can result in defective clonal hematopoietic stem cell proliferation in addition to bone marrow microenvironment alteration. The "bad seeds in bad soil" theory illustrates the orchestrating efforts of hematopoietic stem cells, stromal cells, and their surrounding signaling molecules in myelofibrosis progression and malignancy transformation, though the exact mechanism of myelofibrosis is still not clear. This study reviews current concepts and questions regarding the pathogenesis of primary myelofibrosis and discusses the emerging targeted therapy aimed at restoring normal bone marrow environment and halting bone marrow fibrotic deterioration.

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          Author and article information

          Journal
          Ann. Hematol.
          Annals of hematology
          Springer Nature
          1432-0584
          0939-5555
          Apr 2017
          : 96
          : 4
          Affiliations
          [1 ] Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
          [2 ] Department of Medicine, Penn State University College of Medicine, Hershey, PA, USA.
          [3 ] Department of Medicine, Penn State University College of Medicine, Hershey, PA, USA. jpu2@jhmi.edu.
          [4 ] Department of Pathology, Pennsylvania State University College of Medicine, Hershey, PA, USA. jpu2@jhmi.edu.
          [5 ] Penn State Hershey Cancer Institute, Pennsylvania State University College of Medicine, Hershey, PA, USA. jpu2@jhmi.edu.
          Article
          10.1007/s00277-016-2785-9
          10.1007/s00277-016-2785-9
          27539616
          30f97209-677e-4127-a33c-21b1a2642191
          History

          Genetic and epigenetic abnormality,Hematopoietic bone marrow stem cell,Primary myelofibrosis,Target therapy,Bone marrow microenvironments

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