急性
白血病患者中有
70%到
80%的人都会复发。其原因是数量极少的白血病干细胞反复分裂,使白血病细胞大量增殖。抗癌药物虽然能够杀灭白血病细胞,但难以杀灭其中的白血病干细胞,造成急性白血病屡治屡发。东京大学教授黑川峰夫等人注意到,急性白血病复发患者体内的基因
“Evi-
1”在造血干细胞中非常活跃,他们推测这一基因可能同样作用于白血病干细胞,使其不断分裂,导致白血病细胞大量增殖。
研究小组从患白血病的实验鼠体内取出白血病细胞,去除了
“Evi-
1”基因后再移植到
10只健康实验鼠体内。研究小组还给另外
10只健康实验鼠完整移植了白血病细胞(含
“Evi-
1”)。结果发现,前一组实验鼠比后一组实验鼠平均晚发病一个月;而在杀灭两组实验鼠体内的白血病细胞后,前一组实验鼠没有复发急性白血病,后一组却再次发病。(
Bioon.com)
研究人员认为,对照实验已经说明,
“Evi-
1”对急性白血病的发作和复发有推动作用,而这与它作用于白血病干细胞有直接关系。(
生物谷Bioon.com)
生物谷
推荐原始出处:
Cell Stem Cell
,
Vol 3, 207-220, 07 August 2008,
usumu Goyama, Mineo Kurokawa
Evi-1 Is a Critical Regulator for Hematopoietic Stem Cells and Transformed Leukemic Cells
1
Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, The University of Tokyo Hospital,
2
Department of Cell Therapy and Transplantation Medicine, Graduate School of Medicine, University of Tokyo, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan
3
Department of Regeneration Medicine for Hematopoiesis, Graduate School of Medicine, University of Tokyo, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan
Corresponding author
Mineo Kurokawa
kurokawa-tky@umin.ac.jp
Summary
Evi-1 has been recognized as one of the dominant oncogenes associated with murine and human myeloid leukemia. Here, we show that hematopoietic stem cells (HSCs) inEvi-1-deficient embryos are severely reduced in number with defective proliferative and repopulating capacity. Selective ablation of Evi






