Krishna Narla R, Navara C, Sarquis M, Uckun F M
Parker Hughes Cancer Center, Children's Cancer Group ALL Biology Reference Laboratory and Department of Oncology, Parker Hughes Institute, St. Paul, MN 55113, USA.
Leuk Lymphoma. 2001 May;41(5-6):615-23. doi: 10.3109/10428190109060352.
The TEL-AML1 fusion which results from a cryptic t(12;21) translocation is the most frequently occurring genetic abnormality in childhood acute lymphoblastic leukemia (ALL) and has been associated with an excellent treatment outcome. In the present study, we examined the FAS/BCL-2 expression profiles and chemosensitivity of primary leukemic cells from children with newly diagnosed t(12;21)TEL-AML1 fusion transcript-positive versus t(12;21)TEL-AML1 fusion transcript-negative standard risk ALL. TEL-AML1(+) ALL cells expressed higher levels of the pro-apoptotic protein Fas and lower levels of the anti-apoptotic protein Bcl2 than TEL-AML1(-) ALL cells, as determined by confocal laser scanning microscopy. TEL-AML1(+) ALL cells were more sensitive to the apoptosis-inducing effects of serum deprivation, dexamethasone and vincristine than TEL-AML1(-) ALL cells. This study provides novel mechanistic insights regarding the chemosensitivity of TEL-AML1(+) ALL cells and provides a cogent explanation for the excellent leukemia-free survival outcome of children with TEL-AML1(+) ALL treated on contemporary chemotherapy programs.
由隐匿性t(12;21)易位导致的TEL-AML1融合是儿童急性淋巴细胞白血病(ALL)中最常见的基因异常,并且与良好的治疗结果相关。在本研究中,我们检测了新诊断的t(12;21)TEL-AML1融合转录本阳性与t(12;21)TEL-AML1融合转录本阴性的标准风险ALL患儿原代白血病细胞的FAS/BCL-2表达谱和化疗敏感性。通过共聚焦激光扫描显微镜测定,与TEL-AML1(-) ALL细胞相比,TEL-AML1(+) ALL细胞表达更高水平的促凋亡蛋白Fas和更低水平的抗凋亡蛋白Bcl2。与TEL-AML1(-) ALL细胞相比,TEL-AML1(+) ALL细胞对血清剥夺、地塞米松和长春新碱的凋亡诱导作用更敏感。本研究为TEL-AML1(+) ALL细胞的化疗敏感性提供了新的机制见解,并为接受当代化疗方案治疗的TEL-AML1(+) ALL患儿无白血病生存的良好结果提供了有力解释。