Acute promyelocytic leukemia cell line AP-1060 established as a cytokine-dependent culture from a patient clinically resistant to all-trans retinoic acid and arsenic trioxide

作者：Sun Y; Kim SH; Zhou DC; Ding W; Paietta E; Guidez F; Zelent A; Ramesh KH; Cannizzaro L; Warrell RP; Gallagher RE^*

来源：Leukemia, 2004, 18(7): 1258-1269.

DOI：10.1038/sj.leu.2403372

• acute promyelocytic leukemia
• cell strain immortalization
• cytokine-dependent cell line
• retinoic acid resistance
• arsenic trioxide resistance

AP-1060 is a newly established acute promyelocytic leukemia (APL) cell line from a multiple-relapse patient clinically resistant to both all-trans retinoic acid ( ATRA) and arsenic trioxide (ATO). The line was initially derived as a granulocyte colony-stimulating factor-dependent strain that underwent replicative senescence and, following ethylnitrosourea treatment, as a phenotypically similar immortalized line. Immortalization was associated with broadened cytokine sensitivity but not growth autonomy, in contrast to three previously derived APL lines. Both the AP-1060 strain and line had shortened telomeres and low telomerase activity, while the line had higher expression of many genes associated with macromolecular synthesis. The karyotype was 46, XY, t( 3; 14)( p21.1; q11.2), t( 15; 17)( q22; q11) [100%]; the unique t( 3; 14) was observed in 4/9 t( 15; 17)-positive metaphase cells at previous relapse on ATRA therapy. The PML-RARalpha mRNA harbored a missense mutation in the RARalpha-region ligand-binding domain (Pro900Ser). This was associated with a right-shift and sharpening of the ATRA-induced maturation response compared to ATRA-sensitive NB4 cells, which corresponded to the transcriptional activation by PML-RARalpha(ω) over bar -Pro900Ser of a cotransfected ATRA-targeted reporter vector in COS-1 cells. AP-1060 also manifested relative resistance to ATO-induced apoptosis at greater than or equal to1 muM, while 0.25 muM ATO stimulated limited atypical maturation. These findings suggest that AP-1060 will be useful for further assessing molecular elements involved in APL progression and drug response/resistance.

• 出版日期2004-7