Advances in Clinical and Experimental Medicine
2006, vol. 15, nr 5, September-October, p. 881–887
Publication type: review article
Language: Polish
WT1 – nowy marker komórek białaczkowych
WT1 – a New Marker of Leukaemic Cells
1 Katedra i Klinika Hematologii CM UJ w Krakowie
Streszczenie
Gen WT1 znajduje się na chromosomie 11p13 i koduje czynnik transkrypcyjny o budowie palca cynkowego dla białek odpowiedzialnych za regulację wzrostu i różnicowania komórkowego. Jego ekspresję wykazano podczas rozwoju embrionalnego różnych tkanek zwierzęcych, a także w tkankach nowotworowych u ludzi oraz w ostrych białaczkach. Ekspresja WT1 na komórkach blastycznych większości ostrych białaczek i jej brak na prawidłowych komórkach hemopoetycznych, w tym komórkach progenitorowych CD34+ pozwala na użycie go jako nowego markera służącego do oceny minimalnej choroby resztkowej u chorych na ostre białaczki. Nadekspresję genu WT1 wykazano w przewlekłej białaczce szpikowej oraz guzach litych. Białko WT1 indukuje wytwarzanie swoistych cytotoksycznych limfocytów T i może być antygenem docelowym w celowanej immunoterapii chorób nowotworowych.
Abstract
The WT1 gene is located on chromosome 11p13 and encodes a zinc finger motif−containing transcription factor involved in regulation of growth and differentiation. Its expression was shown during embryonic development in various tissues in animal models as well as in a few human malignancies including acute leukemias. Its expression in the majority of human acute leukemias but not in normal mononuclear blood cells and normal CD34+ hematopoietic progenitors qualifies the WT1 gene transcript as a ‘pan−acute leukemic’ marker probably useful in monitoring minimal residual disease after chemotherapy. WT1 is overexpressed in chronic myeloid leukemia and various types of solid tumors, and the WT1 protein was demonstrated to be an attractive target antigen for immunotherapy against these malignancies induceing WT1−specific cytotoxic T lymphocytes.
Słowa kluczowe
embriogeneza, leukemogeneza, ostre białaczki, MDS, PBS, minimalna choroba resztkowa, immunoterapia
Key words
embryogenesis, leukaemogenesis, acute leukaemias, MDS, CML, minimal residual disease, immunotherapy
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