Modulation of p53, WAF1/p21 and BCL-2 expression during retinoic acid-induced differentiation of NB4 promyelocytic cells

Leuk Res. 1997 May;21(5):439-47. doi: 10.1016/s0145-2126(96)00085-9.

Abstract

The NB4 cell line, established from a patient with APL, carries the t(15; 17) and undergoes differentiation along the granulocytic pathway when exposed to retinoic acid (RA). The NB4 cell line was used as a model for exploring the expression of genes and proteins implicated in growth regulation, differentiation and apoptosis during treatment with RA. NB4 cells undergo a series of cytological and molecular alterations during RA treatment--Day 1: cell differentiation marked by an increase in CD11b is evident. Day 2: WAF1/p21 mRNA and then protein rise, though they drop 2 days later. Day 3: the percentage of cells in S phase begins to decrease and G1 arrest begins. Day 4: p53 mRNA level and then protein levels fall. Day 5: CD11b/BCL-2 double staining cells are markedly reduced. No signs of apoptosis were observed after up to 8 days of treatment with RA. These results demonstrate that NB4 cells treated with RA rapidly differentiate and arrest at G1 phase concurrent with p53-independent WAF1/p21 induction; in addition, phenotypic differentiation appears to commence before changes in cell cycle progression. An explanation for the decrease in p53 as well as the lack of apoptosis immediately after BCL-2 downregulation will require further study.

MeSH terms

  • Antigens, CD / biosynthesis
  • Apoptosis / drug effects
  • Burkitt Lymphoma
  • Cell Cycle / drug effects
  • Cell Differentiation*
  • Cell Division / drug effects
  • Cell Line
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / biosynthesis*
  • Enzyme Inhibitors
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Genes, bcl-2
  • Genes, p53
  • Humans
  • Kinetics
  • Leukemia, Promyelocytic, Acute / pathology*
  • Macrophage-1 Antigen / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis*
  • RNA, Messenger / biosynthesis
  • Time Factors
  • Transcription, Genetic / drug effects
  • Tretinoin / pharmacology*
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / biosynthesis*

Substances

  • Antigens, CD
  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Enzyme Inhibitors
  • Macrophage-1 Antigen
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • Tumor Suppressor Protein p53
  • Tretinoin