Fu Chengcheng, Chen Zixing
First Affiliated Hospital, Suzhou University, Jiangsu Institute of Hematology, Suzhou 215006, China.
Chin Med J (Engl). 2002 Oct;115(10):1475-8.
To study telomerase activity (TA) and its variation in bone marrow mononuclear cells from patients with myelodysplastic syndrome (MDS) at different stages in comparison with normal bone marrow cells and leukemic cells.
The TA was semi-quantitatively determined in mononuclear cells from 20 normal bone marrow samples, 21 patients with MDS at different stages and 32 cases of acute leukemia by using a polymerase chain reaction-enzyme linked immuno-sorben assay (PCR-ELISA) kit.
The TA in normal bone marrow cells was in the range of 0 to 0.3 units (U) with a mean of 0.11 +/- 0.08 U. Among them, 3 samples were considered positive in accordance with the standard recommended by the kit's pamphlet. In bone marrow cells from patients with acute leukemia, the TA was ranging from 0 to 0.96 U with a mean value of 0.42 +/- 0.26 U. The positive rate was 78.1% which was significantly different from that in normal bone marrow (BM) (P < 0.01). In case of myelodysplastic syndrome, the average level of TA was 0.27 +/- 0.19 U (ranging from 0 to 0.97 U) with a positive rate of 66.7%. In comparison with normal BM cells, the difference was significant (P < 0.05). Particularly, the MDS high-risk subgroup exhibited a significantly higher activity of telomerase (P < 0.05). In comparison with INT-1 and INT-2 subgroups in MDS patients based on international prognostic scoring system (IPPS), the difference in TA was also significant (P < 0.05). The abnormality in cell karyotype was not correlated with TA.
The normal bone marrow cells demonstrate TA at a marginal level while a remarkably increasing level may be seen in acute leukemia patients. The BM cells from MDS patients display a moderate TA among which the high risk MDS subgroup with a poor prognostic IPPS score exhibited markedly higher TA.
研究骨髓增生异常综合征(MDS)患者不同阶段骨髓单个核细胞中端粒酶活性(TA)及其变化,并与正常骨髓细胞和白血病细胞进行比较。
采用聚合酶链反应-酶联免疫吸附测定(PCR-ELISA)试剂盒,对20例正常骨髓样本、21例不同阶段的MDS患者及32例急性白血病患者的单个核细胞中端粒酶活性进行半定量测定。
正常骨髓细胞中端粒酶活性在0至0.3单位(U)之间,平均为0.11±0.08 U。其中,按照试剂盒说明书推荐标准,3份样本被判定为阳性。急性白血病患者骨髓细胞中端粒酶活性范围为0至0.96 U,平均值为0.42±0.26 U,阳性率为78.1%,与正常骨髓相比差异有统计学意义(P<0.01)。骨髓增生异常综合征患者中端粒酶活性平均水平为0.27±0.19 U(范围为0至0.97 U),阳性率为66.7%,与正常骨髓细胞相比差异有统计学意义(P<0.05)。特别是MDS高危亚组端粒酶活性明显更高(P<0.05)。与基于国际预后评分系统(IPSS)的MDS患者INT-1和INT-2亚组相比,端粒酶活性差异也有统计学意义(P<0.05)。细胞染色体核型异常与端粒酶活性无关。
正常骨髓细胞端粒酶活性处于较低水平,而急性白血病患者端粒酶活性显著升高。MDS患者骨髓细胞端粒酶活性呈中等水平,其中IPSS预后评分差的高危MDS亚组端粒酶活性明显更高。