Ohyashiki J H, Ohyashiki K, Iwama H, Hayashi S, Toyama K, Shay J W
First Department of Internal Medicine, Tokyo Medical College, 6-7-1 Nishi-shinjuku, Shinjuku-ju, Tokyo 160, Japan.
Clin Cancer Res. 1997 Apr;3(4):619-25.
In the present study, we used the telomeric repeat amplification protocol assay, an internal telomerase assay standard, and an automatic DNA sequencer to detect and quantitate telomerase activity in blood samples obtained from normal and acute leukemia patients. Telomerase activity was analyzed in 78 acute leukemia patients and ranged from 0.65 to 147 relative to the internal standard. Compared to the age-matched normal levels of telomerase activity in the peripheral blood cells, we determined that 45 (81.8%) of 55 acute myeloid leukemia (AML) and 16 (69.6%) of 23 acute lymphoid leukemia patients had elevated telomerase activity. There was no relationship between peak telomere length and telomerase activity in both acute lymphoid leukemia and AML patients. In AML, the level of telomerase activity was associated with French-American-British subtypes and cytogenetics, and patients with elevated telomerase activity had high leukocyte counts and more frequent extramedullary involvement during the disease. Among 78 patients, 5 had high levels of telomerase activities similar to immortalized leukemia cell lines; these 5 patients had a very poor prognosis (P < 0.05). The levels of telomerase activity significantly decreased in patients in complete remission. Most of the patients in complete remission showed a normal level of telomerase activity; however, two of them had low to moderate telomerase activity, and they relapsed shortly after entering complete remission. In relapsed patients, there is a general trend for increased telomerase levels, and 2 of the 13 patients retained high telomerase activity, whereas the other 11 had normal to moderate telomerase activity. These results suggest that telomerase activity may be a useful additional method for monitoring the disease condition in acute leukemia patients.
在本研究中,我们使用端粒重复序列扩增协议检测法、一种内部端粒酶检测标准以及一台自动DNA测序仪,来检测和定量从正常人和急性白血病患者采集的血液样本中的端粒酶活性。对78例急性白血病患者的端粒酶活性进行了分析,相对于内标,其活性范围为0.65至147。与年龄匹配的外周血细胞中端粒酶活性的正常水平相比,我们确定55例急性髓系白血病(AML)患者中有45例(81.8%)以及23例急性淋巴细胞白血病患者中有16例(69.6%)的端粒酶活性升高。在急性淋巴细胞白血病和AML患者中,端粒峰值长度与端粒酶活性之间均无关联。在AML中,端粒酶活性水平与法美英亚型及细胞遗传学相关,端粒酶活性升高的患者白细胞计数高,且在疾病期间髓外浸润更频繁。在78例患者中,有5例的端粒酶活性水平与永生化白血病细胞系相似;这5例患者预后极差(P < 0.05)。完全缓解患者的端粒酶活性水平显著降低。大多数完全缓解患者的端粒酶活性水平正常;然而,其中有2例患者的端粒酶活性为低至中度,并且在进入完全缓解后不久复发。在复发患者中,端粒酶水平总体呈升高趋势,13例患者中有2例保持高端粒酶活性,而其他11例患者的端粒酶活性为正常至中度。这些结果表明,端粒酶活性可能是监测急性白血病患者病情的一种有用的辅助方法。