High levels of lung resistance related protein mRNA in leukaemic cells from patients with acute myelogenous leukaemia are associated with inferior response to chemotherapy and prior treatment with mitoxantrone

Citation
Dw. Xu et al., High levels of lung resistance related protein mRNA in leukaemic cells from patients with acute myelogenous leukaemia are associated with inferior response to chemotherapy and prior treatment with mitoxantrone, BR J HAEM, 106(3), 1999, pp. 627-633
Citations number
34
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BRITISH JOURNAL OF HAEMATOLOGY
ISSN journal
00071048 → ACNP
Volume
106
Issue
3
Year of publication
1999
Pages
627 - 633
Database
ISI
SICI code
0007-1048(199909)106:3<627:HLOLRR>2.0.ZU;2-3
Abstract
Expression of the mdr1 (multidrug resistance), mrp (multidrug resistance as sociated protein), and lrp (lung resistance related protein! genes is assoc iated with transport related MDR (multidrug resistance). We quantified mRNA levels of these genes using competitive reverse transcription polymerase c hain reaction (RT-PCR) in 128 samples of leukaemic cells from 92 patients w ith acute myelogenous leukaemia (AML). There was a wide variation between the samples in mRNA levels of all three genes, The mean mdr1 mRNA level was 1.3 transcripts per cell (range undetec table to 15.8), the mean mrp level was 7.9 (range 0.1-36.2) and mean lrp 3. 9 (range 0.1-29). Lrp mRNA levels were higher in samples drawn at diagnosis from the 15 patie nts with resistant disease than from the 37 with chemosensitive disease (4. 9 SD 3.1 v 2.9 SD 2.3, P=0.016). Neither mdr1 nor mrp mRNA levels were pred ictive for response to chemotherapy. In samples from patients who had recei ved chemotherapy, those that had received mitoxantrone (n = 24) had higher lrp mRNA levels (mean 4.8, SD 2.5) than those that had not (n = 20, mean 2. 8, SD 2.4, P=0.012). In conclusion, the results indicate that lrp expression is associated with inferior response to chemotherapy in AML and that lrp expression increases after exposure to mitoxantrone.