Literature DB >> 12627846

Pathogenesis of selective expansion of PNH clones.

Hideki Nakakuma1, Tatsuya Kawaguchi.   

Abstract

Hemolysis, a characteristic of paroxysmal nocturnal hemoglobinuria (PNH), is caused by the expansion of an affected stem cell with a mutation of the PIG-A gene. Increasing evidence has shown that the presence of the PIG-A mutation alone does not induce the expansion. Two theories have been proposed. One, the growth advantage hypothesis, is supported by current data indicating the presence of several intrinsic alterations that might confer a proliferative advantage to PNH clones over normal cells. Alternatively, the PIG-A mutation might confer a relative survival advantage to PNH clones. This theory is supported by clinical observation indicating that PIG-A mutant cells survive immune-mediated bone marrow injury in patients with aplastic anemia, PNH, and myelodysplastic syndromes. The latter theory is also supported by current experimental data indicating that PIG-A mutant cells are relatively resistant to cytotoxic attack by natural killer cells and cytotoxic T-lymphocytes. The 2 theories appear complementary rather than mutually exclusive. Rapid progress in this field can be expected in the near future.

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Year:  2003        PMID: 12627846     DOI: 10.1007/bf02983210

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  39 in total

1.  Preferential hematopoiesis by paroxysmal nocturnal hemoglobinuria clone engrafted in SCID mice.

Authors:  N Iwamoto; T Kawaguchi; K Horikawa; S Nagakura; T Kagimoto; T Suda; K Takatsuki; H Nakakuma
Journal:  Blood       Date:  1996-06-15       Impact factor: 22.113

2.  Paroxysmal nocturnal haemoglobinuria: long-term follow-up and prognostic factors. French Society of Haematology.

Authors:  G Socié; J Y Mary; A de Gramont; B Rio; M Leporrier; C Rose; P Heudier; H Rochant; J Y Cahn; E Gluckman
Journal:  Lancet       Date:  1996-08-31       Impact factor: 79.321

3.  Cyclosporin-responsive pancytopenia and HLA class II alleles of a patient with paroxysmal nocturnal hemoglobinuria.

Authors:  K Horikawa; S Fujisao; N Iwamoto; S Nagakura; T Kawaguchi; Y Nishimura; K Takatsuki; H Nakakuma
Journal:  Int J Hematol       Date:  1996-02       Impact factor: 2.490

4.  Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes.

Authors:  D E Dunn; P Tanawattanacharoen; P Boccuni; S Nagakura; S W Green; M R Kirby; M S Kumar; S Rosenfeld; N S Young
Journal:  Ann Intern Med       Date:  1999-09-21       Impact factor: 25.391

5.  Resistance to apoptosis caused by PIG-A gene mutations in paroxysmal nocturnal hemoglobinuria.

Authors:  R A Brodsky; M S Vala; J P Barber; M E Medof; R J Jones
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

6.  Increased sensitivity to complement and a decreased red blood cell life span in mice mosaic for a nonfunctional Piga gene.

Authors:  G Tremml; C Dominguez; V Rosti; Z Zhang; P P Pandolfi; P Keller; M Bessler
Journal:  Blood       Date:  1999-11-01       Impact factor: 22.113

Review 7.  Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria.

Authors:  D J Araten; D Swirsky; A Karadimitris; R Notaro; K Nafa; M Bessler; H T Thaler; H Castro-Malaspina; B H Childs; F Boulad; M Weiss; N Anagnostopoulos; A Kutlar; D G Savage; R T Maziarz; S Jhanwar; L Luzzatto
Journal:  Br J Haematol       Date:  2001-11       Impact factor: 6.998

8.  Two cases showing clonal progression with full evolution from aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome to myelodysplastic syndromes and leukemia.

Authors:  S Ishihara; H Nakakuma; T Kawaguchi; S Nagakura; K Horikawa; M Hidaka; N Asou; H Mitsuya
Journal:  Int J Hematol       Date:  2000-08       Impact factor: 2.490

9.  Natural history of paroxysmal nocturnal hemoglobinuria.

Authors:  P Hillmen; S M Lewis; M Bessler; L Luzzatto; J V Dacie
Journal:  N Engl J Med       Date:  1995-11-09       Impact factor: 91.245

10.  Stress signals activate natural killer cells.

Authors:  Eric O Long; Sumati Rajagopalan
Journal:  J Exp Med       Date:  2002-12-02       Impact factor: 14.307

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  4 in total

Review 1.  New insights into molecular pathogenesis of bone marrow failure in paroxysmal nocturnal hemoglobinuria.

Authors:  Tatsuya Kawaguchi; Hideki Nakakuma
Journal:  Int J Hematol       Date:  2007-07       Impact factor: 2.490

Review 2.  Paroxysmal nocturnal hemoglobinuria: a complement-mediated hemolytic anemia.

Authors:  Amy E DeZern; Robert A Brodsky
Journal:  Hematol Oncol Clin North Am       Date:  2015-03-07       Impact factor: 3.722

3.  Unusual association between increased bone resorption and presence of paroxysmal nocturnal hemoglobinuria phenotype in multiple myeloma.

Authors:  Evangelos Terpos; Michalis Samarkos; Christos Meletis; Effie Apostolidou; Maria Tsironi; Konstantinos Korovesis; Despina Mavrogianni; Nora Viniou; John Meletis
Journal:  Int J Hematol       Date:  2003-11       Impact factor: 2.490

4.  The involvement of adult stem cells originated from bone marrow in the pathogenesis of pterygia.

Authors:  Young Soo Song; Yang Hwan Ryu; Suk Rae Choi; Jae Chan Kim
Journal:  Yonsei Med J       Date:  2005-10-31       Impact factor: 2.759

  4 in total

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