Olszewski M, Huang W, Chou P M, Duerst R, Kletzel M
Stem Cell Processing, Children's Memorial Hospital, Chicago, Illinois 60614, USA.
Cytotherapy. 2005;7(1):57-61. doi: 10.1080/14653240510018046.
Wilms' tumor 1 (WT1) gene expression is seen in a significant number of cases of human neoplasia; however, the mechanism of action remains to be clarified. We hypothesized that WT1 gene is a surrogate marker of proliferation in normal hematopoietic cells and leukemias. While we and others have recognized its value as a tool for the detection of minimal residual disease (MRD), the objective of this study was to confirm our hypothesis regarding normal.
Samples from healthy donors (n=16) and UC blood (n=9) were cultured in Methocult for 21 days. Colonies were analyzed on days 7, 14 and 21 by RT-PCR for WT1 gene expression. Our positive controls were samples from patients with leukemia (n=91). Negative controls were from normal volunteers without stimulation (n=26).
Results showed a statistically significant difference (P<0.0001) between cultured groups, with the highest level of WT1 gene expression in the positive controls and on day 14, when cells are at their maximal proliferation.
In conclusion, WT1 gene expression in the proliferating colonies was highest on day 14, although less than in leukemia samples, confirming our hypothesis that WT1 gene is a surrogate marker of proliferation, not only in leukemogenesis but also, to a lesser degree, in normal cell proliferation.
在大量人类肿瘤病例中可观察到威尔姆斯瘤1(WT1)基因表达;然而,其作用机制仍有待阐明。我们推测WT1基因是正常造血细胞和白血病中增殖的替代标志物。虽然我们和其他人已经认识到其作为检测微小残留病(MRD)工具的价值,但本研究的目的是证实我们关于正常情况的假设。
将来自健康供体(n = 16)和脐血(n = 9)的样本在甲基纤维素培养基中培养21天。在第7天、14天和21天通过逆转录聚合酶链反应(RT-PCR)分析集落中WT1基因的表达。我们的阳性对照是白血病患者的样本(n = 91)。阴性对照来自未受刺激的正常志愿者(n = 26)。
结果显示培养组之间存在统计学显著差异(P < 0.0001),阳性对照中WT1基因表达水平最高,且在第14天,此时细胞处于最大增殖状态。
总之,增殖集落中WT1基因表达在第14天最高,尽管低于白血病样本,这证实了我们的假设,即WT1基因不仅在白血病发生过程中,而且在较小程度上在正常细胞增殖中都是增殖的替代标志物。