Page 1358 - Williams Hematology ( PDFDrive )
P. 1358

1332  Part X:  Malignant Myeloid Diseases                                Chapter 86:  Primary Myelofibrosis          1333




                    65.  Garimella R, Kacena MA, Tague SE, et al: Expression of bone morphogenetic proteins     98.  Apaja-Sarkkinen M, Autio-Harmainen H, Alavaikko M, et al: Immunohistochemical
                     and their receptors in the bone marrow megakaryocytes of GATA-1(low) mice: A pos-  study of basement membrane proteins and type III procollagen in myelofibrosis. Br J
                     sible role in osteosclerosis. J Histochem Cytochem 55:745, 2007.  Haematol 63:571, 1986.
                    66.  Levine RL, Gilliland DG: Myeloproliferative disorders. Blood 112:2190, 2008.    99.  Hasselbalch H, Junker P, Lisse I, et al: Serum markers for type IV collagen and type III
                    67.  Levine RL, Wadleigh M, Cools J, et al: Activating mutation in the tyrosine kinase JAK2   procollagen in the myelofibrosis-osteomyelosclerosis syndrome and other chronic
                     in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelo-  myeloproliferative disorders. Am J Hematol 23:101, 1986.
                     fibrosis. Cancer Cell 7:387, 2005.                   100. Reilly JT: Pathogenesis of idiopathic myelofibrosis: Role of growth factors. J Clin Pathol
                    68.  Kilpivaara O, Levine RL: JAK2 and MPL mutations in myeloproliferative neoplasms:   45:461, 1992.
                     Discovery and science. Leukemia 22:1813, 2008.       101. Charron D, Robert L, Couty MC, Binet JL: Biochemical and histological analysis of
                    69.  Wernig G, Mercher T, Okabe R, et al: Expression of Jak2V617F causes a polycythemia   bone marrow collagen in myelofibrosis. Br J Haematol 41:151, 1979.
                     vera-like disease with associated myelofibrosis in a murine bone marrow transplant     102. Podolak-Dawidziak M, Wróbel T, Jelen M: Serum concentration of the amino terminal
                     model. Blood 107:4274, 2006.                          peptide of type III procollagen (PIIINP) in patients with myeloproliferative disorders
                    70.  Lacout C, Pisani DF, Tulliez M, et al: JAK2V617F expression in murine hematopoi-  (MPD). Pol Arch Med Wewn 99:24, 1998.
                     etic cells leads to MPD mimicking human PV with secondary myelofibrosis.  Blood     103. Gay S, Gay RE, Prohal JT: Immunohistological studies of bone marrow collagen, in
                     108:1652, 2006.                                       Myelofibrosis and the Biology of Connective Tissue, edited by Berk P, Castro-Malaspina
                    71.  Zaleskas VM, Krause DS, Lazarides K, et al: Molecular pathogenesis and therapy of   H, Wasserman LR, p 291. Alan R. Liss, New York, 1984.
                     polycythemia induced in mice by JAK2 V617F. PLoS One 1:e18, 2006.    104. Hasselbalch H, Junker P, Horslev-Patersen K, et al: Procollagen type III amino-terminal
                    72.  Kralovics R, Guan Y, Prchal JT: Acquired uniparental disomy of chromosome 9p is a   peptide in serum in idiopathic myelofibrosis and allied conditions. Am J Hematol 33:18,
                     frequent stem cell defect in polycythemia vera. Exp Hematol 30:229, 2002.  1990.
                    73.  Tiedt R, Hao-Shen H, Sobas MA, et al: Ratio of mutant JAK2-V617F to wild-type Jak2     105. Reilly JT, Nash JRG, Mackie MJ, McVerry BA: Endothelial cell proliferation in myelofi-
                     determines the MPD phenotypes in transgenic mice. Blood 111:3931, 2008.  brosis. Br J Haematol 60:625, 1985.
                    74.  Larsen TS, Pallisgaard N, Møller MB, Hasselbalch HC: The JAK2 V617F allele burden     106. Baglin TP, Crocker MA, Timmins A, et al: Bone marrow hypervascularity in patients
                     in essential thrombocythemia, polycythemia vera and primary myelofibrosis—Impact   with myelofibrosis identified by infrared thermography.  Clin Lab Haematol 13:341,
                     on disease phenotype. Eur J Haematol 79:508, 2007.    1991.
                    75.  Pikman Y, Lee BH, Mercher T, et al: MPLW515L is a novel somatic activating mutation     107. Bock O, Neuse J, Hussein K, et al: Aberrant collagenase expression in chronic idiopathic
                     in myelofibrosis with myeloid metaplasia. PLoS Med 3:e270, 2006.  myelofibrosis is related to the stage of disease but not to the JAK2 mutation status. Am
                    76.  Pardanani AD, Levine RL, Lasho T, et al: MPL515 mutations in myeloproliferative and   J Pathol 169:471, 2006.
                     other myeloid disorders: A study of 1182 patients. Blood 108:3472, 2006.    108. Bock O, Höftmann J, Theophile K, et al: Bone morphogenetic proteins are overex-
                    77.  Tefferi A: JAK and MPL mutations in myeloid malignancies. Leuk Lymphoma 49:388,   pressed in the bone marrow of primary myelofibrosis and are apparently induced by
                     2008.                                                 fibrogenic cytokines. Am J Pathol 172:951, 2008.
                    78.  Tefferi A: Primary myelofibrosis: 2013 update on diagnosis, risk-stratification, and     109. Dolan G, Forrest P, Eastham J, et al: Serum laminin, procollagen terminal peptide III
                     management. Am J Hematol 88:141, 2013.                and thrombocyte platelet derived growth factor concentrations in idiopathic myelofi-
                    79.  Klampfl T, Gisslinger H, Harutyunyan AS, et al: Somatic mutations of calreticulin in   brosis. Br J Haematol 77(Suppl 1):73, 1991.
                     myeloproliferative neoplasms. N Engl J Med 369:2379, 2013.    110. Reilly JT, Nash JRG, Mackie MJ, McVerry BA: Immunoenzymatic detection of fibronec-
                    80.  Nangalia J, Massie CE, Baxter EJ, et al: Somatic CALR mutations in myeloproliferative   tin in normal and pathological haemopoietic tissue. Br J Haematol 59:497, 1985.
                     neoplasms with nonmutated JAK2. N Engl J Med 369:2391, 2013.    111. Hasselbalch H, Clemmensen I: Plasma fibronectin in idiopathic myelofibrosis and
                    81.  Wang L, Swierczek SI, Drummond J, et al: Whole-exome sequencing of polycythemia   related chronic myeloproliferative disorders. Scand J Clin Lab Invest 47:429, 1987.
                     vera revealed novel driver genes and somatic mutation shared by T-cells and granulo-    112. Soini Y, Kamel D, Apaja-Sarkkinen M, et al: Tenascin immunoreactivity in normal and
                     cytes. Leukemia 28:935, 2014.                         pathological bone marrow. J Clin Pathol 46:218, 1993.
                    82.  Abu-Duhier FM, Goodeve AC, Care RS, et al: Mutational analysis of class III recep-    113. Reilly JT, Nash JRG: Vitronectin (serum spreading factor): Its localization in normal
                     tor tyrosine kinases (C-KIT, C-FMS, FLT3) in idiopathic myelofibrosis. Br J Haematol   and fibrotic tissue. J Clin Pathol 41:1269, 1988.
                     120:464, 2003.                                       114. Le Bousse-Kerdilès MC, Martyré MC, et al: Involvement of the fibrogenic cytokines,
                    83.  Kawamata N, Ogawa S, Yamamoto G, et al: Genetic profiling of myeloproliferative dis-  TGF-β and bFGF, in the pathogenesis of idiopathic myelofibrosis. Pathol Biol 49:153,
                     orders by single-nucleotide polymorphism oligonucleotide microarray. Exp Hematol   2001.
                     36(11):1477, 2008.                                   115. Rameshwar P, Oh HS, Yook C, Chang VT: Substance P-fibronectin cytokine interac-
                    84.  Andrieux J, Demory JL, Dupriez B, et al: Dysregulation and overexpression of   tions in myeloproliferative disorders with bone marrow fibrosis. Acta Haematol 109:1,
                     HMGA2 in myelofibrosis with myeloid metaplasia. Genes Chromosomes Cancer 39:82,     2003.
                     2004.                                                116. Wang JC, Wong C, Kao WW: Immunoreactive prolylhydroxylase in patients with pri-
                    85.  Bogani C, Ponziani V, Guglielmelli P, et al: Myeloproliferative Disorders Research Con-  mary and secondary myelofibrosis. Br J Haematol 65:171, 1987.
                     sortium. Hypermethylation of CXCR4 promoter in CD34+ cells from patients with     117. Barosi G, Costa A, Liberato LN, et al: Serum procollagen III peptide level correlates
                     primary myelofibrosis. Stem Cells 26:1920, 2008.      with disease activity in myelofibrosis with myeloid metaplasia. Br J Haematol 72:16,
                    86.  Rosti V, Massa M, Vannucchi AM, et al: The expression of CXCR4 is down-regulated on   1989.
                     the CD34+ cells of patients with myelofibrosis with myeloid metaplasia. Blood Cells Mol     118. Hochweiss S, Fruchtman S, Hahn EG, et al: Increased serum procollagen III amino-
                     Dis 38:280, 2007.                                     terminal peptide in myelofibrosis. Am J Hematol 15:343, 1983.
                    87.  Ciurea SO, Merchant D, Mahmud N, et al: Pivotal contributions of megakaryocytes to     119. Hasselbalch H, Junker P, Lisse I, et al: Circulating hyaluronan in the myelofibrosis/oste-
                     the biology of idiopathic myelofibrosis. Blood 110:986, 2007.  omyelosclerosis syndrome and other myeloproliferative disorders. Am J Hematol 36:1,
                    88.  Guglielmelli P, Zini R, Bogani C, et al: Molecular profiling of CD34+ cells in idiopathic   1991.
                     myelofibrosis identifies a set of disease-associated genes and reveals the clinical signifi-    120. Thiele J, Kvasnicka HM, Fischer R, Diehl V: Clinicopathological impact of the inter-
                     cance of Wilms’ tumor gene 1 (WT1). Stem Cells 25:165, 2007.  activity between megakaryocytes and myeloid stroma in chronic myeloproliferative
                    89.  Massa M, Rosti V, Ramajoli I, et al: Circulating CD34+, CD133+, and vascular endothe-  disorders: A concise update. Leuk Lymphoma 24:463, 1997.
                     lial growth factor receptor 2-positive endothelial progenitor cells in myelofibrosis with     121. Schmitt A, Drouin A, Masse J-M, et al: Polymorphonuclear neutrophil and megakary-
                     myeloid metaplasia. J Clin Oncol 23:5688, 2005.       ocyte mutual involvement in myelofibrosis pathogenesis.  Leuk  Lymphoma 43:719,
                    90.  Rosti V, Villani L, Riboni R, et al: Spleen endothelial cells from patients with myelofi-  2002.
                     brosis harbor the JAK2V617F mutation. Blood 121:360, 2013.    122. Frey BM, Rafii S, Teterson M, et al: Adenovector-mediated expression of human throm-
                    91.  Giraudier S, Chagraoui H, Komura E, et al: Overexpression of FKBP51 in idiopathic   bopoietin cDNA in immune-compromised mice: Insights into the pathophysiology of
                     myelofibrosis regulates the growth factor independence of megakaryocyte progenitors.   osteomyelofibrosis. J Immunol 160:691, 1998.
                     Blood 100:2932, 2002.                                123. Rameshwar  P,  Chang  VT,  Thacker  UF,  Gascón  P:  Systemic  transforming  growth
                    92.  Wang JC, Chen C, Lou LH, et al: Blood thrombopoietin, IL-6, and IL-11 levels in   factor-beta in patients with bone marrow fibrosis-pathophysiological implications. Am
                     patients with agnogenic myeloid metaplasia. Leukemia 11:1827, 1997.  J Hematol 59:133, 1998.
                    93.  Moliterno AR, Hankins WD, Spivak JL: Impaired expression of the thrombopoietin     124. Rosenfeld M, Keating A, Bowen-Pope BF, et al: Responsiveness of the in vitro hemato-
                     receptor by patients with polycythemia vera. N Engl J Med 338:572, 1998.  poietic microenvironment to platelet-derived growth factor. Leuk Res 9:427, 1985.
                    94.  Prockop DJ, Kivirikko KI, Tuderman L, et al: The biosynthesis of collagen and its disor-    125. Bernabei PA, Arcangeli A, Casini M, et al: Platelet-derived growth factor(s) mitogenic
                     ders. N Engl J Med 301:13, 1979.                      activity in patients with myeloproliferative disease. Br J Haematol 63:353, 1986.
                    95.  Bauermeister DE: Quantitation of bone marrow reticulin: A normal range. Am J Clin     126. Thiele J, Rompick V, Wagner S, Fischer R: Vascular architecture and collagen type IV in
                     Pathol 56:24, 1971.                                   primary myelofibrosis and polycythemia vera. Br J Haematol 80:227, 1992.
                    96.  Ivànyi JL, Mahunka M, Papp A, Telek B: Prognostic significance of bone marrow retic-    127. Johnston JB, Dalal BI, Israels SJ, et al: Deposition of transforming growth factor-β in the
                     ulum fibers in idiopathic myelofibrosis: Evolution of clinicopathological parameters in   marrow in myelofibrosis, and the intracellular localization and secretion of TGF-β by
                     a scoring system. Haematologica 26:75, 1994.          leukemic cells. Am J Clin Pathol 103:574, 1995.
                    97.  McCarthy DM: Annotation: Fibrosis of the bone marrow: Content and causes. Br J     128. Martré M-C: TGF-β and megakaryocytes in the pathogenesis of myelofibrosis in mye-
                     Haematol 59:1, 1985.                                  loproliferative disorders. Leuk Lymphoma 20:39, 1995.







          Kaushansky_chapter 86_p1319-1340.indd   1333                                                                  9/18/15   10:24 AM
   1353   1354   1355   1356   1357   1358   1359   1360   1361   1362   1363