Cell proliferation is related to in vitro drug resistance in childhood acute leukaemia
British Journal of Cancer , Volume 88 - Issue 5 p. 775- 781
Bone marrow and peripheral blood samples from 362 patients with acute lymphoblastic leukaemia (ALL) proliferating cell and 90 patients with acute myeloid leukaemia (AML) were analysed for S-phase fractions, Ki67 antigen, and proliferating cell nuclear antigen expression. The S-phase fractions were correlated with in vitro drug resistance to 15 different anticancer agents. Leukaemia cells isolated from bone marrow had higher S-phase fractions than leukaemia cells isolated from peripheral blood (in initial ALL, median values resp. 6.9 and 2.7%, in initial AML resp, 5.3 and 1.3%; both P < 0.01). Relapse ALL samples derived from bone marrow showed increased S-phase fractions (median 9.9%) compared with initial ALL samples (median 6.9%; P < 0.01). ALL samples obtained at initial diagnosis showed higher S-phase fractions (median 6.9%) and higher Ki67 expression (median 30%) than initial AML samples (median resp. 5.3 and 14%; both P < 0.05). The S-phase fractions were not related to white blood cell count, age, or gender. Within initial ALL, the S-phase fraction correlated significantly but modestly strong (p = 0.3-0.5; P < 0.05) with sensitivity to antimetabolites (cytarabine, mercaptopurine, thioguanine), L-asparaginase. teniposide, and vincristine. Similar results were found within subgroups of initial ALL (nonhyperdiploid and common/precursor-B-lineage ALL). In relapsed ALL and AML such correlations were not found. In conclusion, cell proliferation differs between leukaemia subgroups and increased proliferation is associated with increased in vitro sensitivity to several anticancer agents in initial ALL.
|British Journal of Cancer|
|Organisation||Department of Pediatrics|
Kaaijk, P, Creutzig, U, Veerman, A.J.P, Kaspers, G.J.L, van Wering, E.R, Broekema, G.J, … Henze, G. (2003). Cell proliferation is related to in vitro drug resistance in childhood acute leukaemia. British Journal of Cancer, 88(5), 775–781. doi:10.1038/sj.bjc.6600787