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Blood, 15 December 2006, Vol. 108, No. 13, pp. 3960-3961. This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Alert me to new issues of the journal Download to citation manager Rights and Permissions Citing Articles Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by Rosse, W. F. Search for Related Content PubMed Articles by Rosse, W. F. Related Collections Related Article in Blood Online Social Bookmarking                   What's this?  Previous Article  |  Table of Contents  |  Next Article  RED CELLS Comment on Inoue et al, page 4232 How many mutations does it take to get PNH? Wendell F. Rosse DUKE UNIVERSITY One of the puzzles in understanding paroxysmal nocturnal hemoglobinuria is the reason for the expansion of the defective clone. In this issue, Inoue and colleagues suggest that a second mutation might be needed. The characteristic biochemical lesion in paroxysmal nocturnal hemoglobinuria (PNH) is the clonal lack of glycosyl phosphatidylinositol (GPI)–linked proteins on the membrane of the affected blood cells. This lesion accounts for many of the clinical manifestations of the disease, particularly intravascular hemolysis and its consequences and, probably, the marked propensity for venous thromboses. The lesion results from mutations of the gene, called PIGA, that codes for one of the components necessary for the biosynthesis of the GPI anchor. Hematopoietic precursors with defects in this gene have been identified in many if not most healthy donors tested, so it is clear that this mutation is not enough to account for the occurrence of the disease. The PNH clone must be selected and expanded in order for a sufficient number of blood cells to be present to cause clinical manifestations. It has been suggested that the clone is selected for by the immunologic processes underlying aplastic anemia (the Luzzatto-Young hypothesis) and, indeed, a large proportion of patients with aplastic anemia exhibit the cells characteristic of PNH, albeit usually in relatively small proportions. In only a minority of such patients does the clone expand to clinical relevance. Thus, neither the characteristic biochemical abnormality nor the selection process explains requisite expansion of the clone in those patients with PNH. In their paper, Inoue and colleagues offer a possible insight into this problem. In 2 patients, the authors have found a rearrangement of chromosome 12 that has apparently induced a mutation causing the "deregulation" of the HMGA2 gene. This gene produces a protein, a member of the high-mobility group of proteins, that functions as an architectural transcription factor, promoting transcription by facilitation of the assembly of transcription factors into an "enhanceosome." Mutations causing deregulation of the gene have been found in benign mesenchymal tumors. Inoue et al argue that in these 2 patients, overactivity of the HMGA2 gene as a consequence of the chromosomal break gives the selected PIGA–mutated clone the expansion that it needs to become clinically manifest but not the uncontrolled expansion of a malignancy. Thus, PNH is viewed as a benign tumor of the bone marrow involving the selected GPI-deficient clone. This paper's importance is that it points to an area of study that may solve one of the 2 basic problems in understanding PNH: the basis of clonal selection and the basis of clonal expansion. Most patients do not have chromosomal abnormalities, and it will be difficult to know where to look for second mutations that are not manifest in such gross ways, but at least the results in these 2 patients suggest a starting point. When more is known, my guess is that the relationship of PNH to myelodysplastic syndromes and to acute leukemia will also be adumbrated. The author declares no competing financial interests. CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    What's this? Related Article in Blood Online: Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH) Norimitsu Inoue, Tomohisa Izui-Sarumaru, Yoshiko Murakami, Yuichi Endo, Jun-Ichi Nishimura, Ken Kurokawa, Maki Kuwayama, Hiroaki Shime, Takashi Machii, Yuzuru Kanakura, Gabrielle Meyers, Carl Wittwer, Zhong Chen, William Babcock, Debra Frei-Lahr, Charles J. Parker, and Taroh Kinoshita Blood 2006 108: 4232-4236. [Abstract] [Full Text] [PDF] This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Alert me to new issues of the journal Download to citation manager Rights and Permissions Citing Articles Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by Rosse, W. F. Search for Related Content PubMed Articles by Rosse, W. F. Related Collections Related Article in Blood Online Social Bookmarking                   What's this?

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