上海第二医科大学学报(英文版)
上海第二醫科大學學報(英文版)
상해제이의과대학학보(영문판)
JOURNAL OF SHANGHAI SECOND MEDICAL UNIVERSITY
2000年
1期
22-26
,共5页
陈烨%缪金明%朱学宏%邵念贤%方智雯%欧阳仁荣
陳燁%繆金明%硃學宏%邵唸賢%方智雯%歐暘仁榮
진엽%무금명%주학굉%소념현%방지문%구양인영
acute promyelocytic leukemia%apoptosis%antisence oligodeoxynucleotides%PML - RARα gene
Objective To investigate the effects of anti- PML/RARα or anti- PML antisence on the growth,differentiation and apoptosis of NB4 cell lines. Methods Wright's stain for cell morphology, flow cytometry and DNA gel electronphoresis for cell apoptosis, methylcellulose assays for leukemic colony forming unit and trypan - blue exclusion for cell counts. Results Both the start cordon region of the PML or PML- RARα mRNA(STAS) and the fusion point region of the long type PML - RARα mRNA (FUAS) could inhibit cell growth. Cells became partially differentiated at 5d of treatment, and FUAS- treated cells showed more significant differentiation than STAS-treated cells. Morphology of typical apoptosis could be seen at 7, 9d incubation with antisence oligodeoxynucleotides (AS). In contrast, no cell growth inhibition, no morphology changes were seen in Sen or Ran treated cells compared with untreated cells. The number of acute myelocytic leukemia colony forming unit(AML - CFU) markedly decreased in STAS and FUAS treated cells. Cell DNA content analyzed by flow cytometry showed the typical profile of apoptotic cells, in which pre- G1 peak appear before G1 peak at 7,9d of treatment with STAS or FUAS. Conclusion Anti-PML/RARα or anti-PML antisence inhibit the cell growth, induce differentiation and differentiated cell apoptosis of NB4 cells.