Abaza H M H, Elmougy M I, El Maraghy H M A, Mahmoud H M
Clinical Pathology Department, Ain Shams University, Cairo, Egypt.
Int J Lab Hematol. 2016 Feb;38(1):81-9. doi: 10.1111/ijlh.12445. Epub 2015 Nov 7.
Stanniocalcin1 (STC1) is a hormone that regulates cell growth and survival; this study aimed to evaluate the STC1 gene expression in patients with acute leukemia and assess its prognostic significance.
Seventy-six patients with acute leukemia were enrolled for determination of mRNA STC1 by real-time quantitative polymerase chain reaction at diagnosis and at day 28.
Median STC1 gene expression was 16.2 and 4.43 in patients with acute myeloid leukemia and 9.67 and 2.37 in patients with acute lymphoblastic leukemia on days 0 and 28, respectively. A cutoff level for STC1 gene expression was established subdividing patients into high- and low-STC1 gene expression groups. Median STC1 gene expression at days 0 and 28 was significantly higher among patients who were nonresponders to therapy than among those who were therapy responders in both groups. Patients achieving complete remission had significantly lower baseline STC1 gene expression than those in relapse. High STC1 gene expression was associated with shorter overall and disease-free survival times.
STC1 gene expression at diagnosis might be a useful prognostic marker for clinical outcome and monitoring therapeutic response in patients with acute leukemia.
鲽源钙素1(STC1)是一种调节细胞生长和存活的激素;本研究旨在评估急性白血病患者中STC1基因的表达情况,并评估其预后意义。
纳入76例急性白血病患者,在诊断时及第28天通过实时定量聚合酶链反应测定STC1 mRNA。
急性髓系白血病患者在第0天和第28天的STC1基因表达中位数分别为16.2和4.43,急性淋巴细胞白血病患者分别为9.67和2.37。确定了STC1基因表达的临界值,将患者分为高STC1基因表达组和低STC1基因表达组。在两组中,治疗无反应者在第0天和第28天的STC1基因表达中位数均显著高于治疗有反应者。达到完全缓解的患者基线STC1基因表达显著低于复发患者。高STC1基因表达与较短的总生存期和无病生存期相关。
诊断时的STC1基因表达可能是急性白血病患者临床结局和监测治疗反应的有用预后标志物。