Literature DB >> 27539616

Primary myelofibrosis and its targeted therapy.

Lindsey Shantzer1, Kristin Berger2, Jeffrey J Pu3,4,5.   

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.

Entities:  

Keywords:  Bone marrow microenvironments; Genetic and epigenetic abnormality; Hematopoietic bone marrow stem cell; Primary myelofibrosis; Target therapy

Mesh:

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Year:  2016        PMID: 27539616     DOI: 10.1007/s00277-016-2785-9

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  2 in total

1.  Impact of ruxolitinib on myelofibrosis patients post allogeneic stem cell transplant-a pilot study.

Authors:  Jeffrey J Pu; Joyson Poulose; Jozef Malysz; Junjia Zhu; Julie C Fanburg-Smith; David F Claxton; Michael G Bayerl
Journal:  Br J Haematol       Date:  2019-05-22       Impact factor: 6.998

Review 2.  BRD4 inhibition for the treatment of pathological organ fibrosis.

Authors:  Matthew S Stratton; Saptarsi M Haldar; Timothy A McKinsey
Journal:  F1000Res       Date:  2017-06-28
  2 in total

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