Clinical significance of leukemia stem/progenitor cell related gene expression in acute leukemia.
- Author:
Hai-Bo ZHU
1
;
Ming-Feng ZHAO
;
Fang XIE
;
Xia XIAO
;
Xin-Nü XU
;
Juan MU
;
Jiao-Wa YANG
;
Peng-Jian LIU
;
Hai-Rong LÜ
;
Yu-Min LI
Author Information
1. Department of Hematology, Tianjin First Central Hospital, Tianjin, China.
- Publication Type:Journal Article
- MeSH:
ATP Binding Cassette Transporter, Sub-Family B;
ATP-Binding Cassette, Sub-Family B, Member 1;
genetics;
metabolism;
Adolescent;
Adult;
Aged;
Female;
Gene Expression;
Homeodomain Proteins;
genetics;
metabolism;
Humans;
Immunophenotyping;
Leukemia, Myeloid, Acute;
genetics;
metabolism;
Male;
Middle Aged;
Neoplastic Stem Cells;
metabolism;
Polycomb Repressive Complex 1;
genetics;
metabolism;
Transcription Factors;
genetics;
metabolism;
Young Adult
- From:
Journal of Experimental Hematology
2011;19(5):1150-1155
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to detect the expression of leukemia stem/progenitor cell (LSPC) related genes (ABCB1, BMI-1, HOXB4) in the patients with acute leukemia, and to explore its clinical significance in acute leukemia. Bone marrow samples were collected from de novo acute leukemia patients (41 cases), patients with complete remission (CR, 16 cases) and the patients with non-malignant hematologic diseases (10 cases) respectively. And the expressions of ABCB1, BMI-1, HOXB4 genes were detected by comparative real-time quantitative PCR (RQ-PCR) with SYBR Green assay. The results showed that the expressions of ABCB1, BMI-1, HOXB4 were not detected in the patients with non-malignant hematologic diseases, but were higher (relative expressive level: 4.26 ± 2.26, 3.72 ± 1.91, 3.74 ± 2.38) in de novo acute leukemia patients and lower (relative expressive level: 2.14 ± 1.47, 2.07 ± 0.99, 1.47 ± 0.89) in the acute leukemia patients with CR (p < 0.05). The expressions of LSPC related genes were lower (relative expressive level: 1.77 ± 1.29, 2.09 ± 1.26, 1.78 ± 1.49) in the patients acquired CR/partial remission (PR) than those in the patients not acquired CR/PR (relative expressive level: 7.23 ± 1.78, 3.96 ± 0.92, 4.48 ± 2.57) (p < 0.01). Univariate analysis revealed that there were more cases with the expression of LSPC immunophenotype (CD34(+)CD38(-)CD96(+) and CD34(+)CD38(-)CD123(+)) and more hyperleukocytosis cases in patients with any higher expression of LSPC related gene (p < 0.05). Analysis of multiple parameters discovered larger significance (p < 0.01). It is concluded that there is a good relationship between LSPC related genes (ABCB1, BMI-1, HOXB4) and LSPC immunophenotype. The expression of LSPC-related genes is higher in de novo acute leukemia patients, and lower in patients acquired CR/PR. The patients with higher expressed LSPC-related genes display worse response to chemotherapy, lower CR/PR rate and higher leukocytosis, the analysis of multiple parameters may be a good method for assessing the therapeutic efficacy/prognosis of acute leukemia.
