Narayan Shashi, Chandra Jagdish, Sharma Meenal, Naithani Rahul, Sharma Sunita
Department of Pathology, Lady Hardinge Medical College, Kalawati Saran Children's Hospital, New Delhi, India.
Hematology. 2007 Feb;12(1):39-43. doi: 10.1080/10245330600938125.
Twenty-five children (19 M:6 F) with newly diagnosed ALL with median age of 5.5 years (1 month-12 years) were enrolled in the study. Apoptosis regulator proteins bcl-2 and bax were measured in all patients using alkaline phosphatase anti-alkaline phosphatase method. Twenty-one patients were positive for bcl-2 and 23 cases for Bax, although expression levels varied. Patients who presented with splenomegaly or hepatomegaly < 5 cm expressed significantly higher levels of bcl-2 and bax protein expression. Neither of age ( < or >10 years), sex, generalized lymphadenopathy, WBC ( < or >50,000/mul) or FAB subtype was associated with high levels of bcl-2 or bax protein expression. Patients with higher mean hemoglobin levels (p = 0.009), high blast % in bone marrow (p = 0.02), immature immunophenotype (p = 0.001) exhibited signifxicantly higher bcl-2 levels. Bcl-2/bax ratio correlated inversely with TLC at presentation (p = 0.022; r = - 0.456) and in B-lineage leukemic cells as compared to T-lineage cells (p = 0.002). Bcl-2/bax ratio did not correlate with any other variable measured. Bcl-2 and bax protein co-express in ALL and high bcl-2/bax ratio correlates with good prognosis features.
25名新诊断为急性淋巴细胞白血病(ALL)的儿童(19名男性,6名女性)纳入本研究,中位年龄为5.5岁(1个月至12岁)。采用碱性磷酸酶抗碱性磷酸酶法检测所有患者的凋亡调节蛋白bcl-2和bax。21例患者bcl-2呈阳性,23例患者Bax呈阳性,尽管表达水平有所不同。出现脾肿大或肝肿大<5cm的患者bcl-2和bax蛋白表达水平明显更高。年龄(<或>10岁)、性别、全身淋巴结肿大、白细胞计数(<或>50,000/μl)或FAB亚型均与bcl-2或bax蛋白高表达无关。平均血红蛋白水平较高(p = 0.009)、骨髓原始细胞百分比高(p = 0.02)、免疫表型不成熟(p = 0.001)的患者bcl-2水平明显更高。bcl-2/bax比值与就诊时的总白细胞计数(TLC)呈负相关(p = 0.022;r = - 0.456),与B系白血病细胞相比,T系细胞中的bcl-2/bax比值也呈负相关(p = 0.002)。bcl-2/bax比值与其他任何测量变量均无相关性。bcl-2和bax蛋白在ALL中共表达,高bcl-2/bax比值与良好的预后特征相关。