Sela B
Department of Pathological Chemistry, Sheva Medical Center, Tel-Hashomer, Department of Clinical Biochemistry, Sackler Faculty of Medicine, Tel-Aviv University, Israel.
Harefuah. 2002 Jan;141(1):103-7, 123.
The recently discovered 16.5 kDa protein survivin was found to inhibit the two early apoptotic enzymes caspase-3 and caspase-7, thus preventing programmed cell death. Survivin may act simultaneously with the bel-2 family proteins, but has a different apoptosis inhibitory mechanism. Numerous reports have demonstrated the expression of survivin in various tumors such as neuroblastoma, melanoma, bladder carcinoma, breast and lung non-small cell tumors, esophegeal and colo-rectal carcinomas and leukemic cells. In contrast, this protein was not traced in adjacent normal tissues by either immunohistochemical staining or by PCR analysis of the expression of survivin mRNA. Importantly, there seems to be a positive correlation between survivin expression and tumor grading, as well as an indication of tumor recurrence after resection or chemotherapy. Potentially, this protein could add to the repertory of diagnostic and prognostic markers in monitoring oncologic patients.
最近发现的16.5 kDa蛋白存活素被发现可抑制两种早期凋亡酶——半胱天冬酶-3和半胱天冬酶-7,从而防止程序性细胞死亡。存活素可能与bcl-2家族蛋白同时发挥作用,但具有不同的凋亡抑制机制。大量报告表明,存活素在各种肿瘤中表达,如神经母细胞瘤、黑色素瘤、膀胱癌、乳腺和肺非小细胞肿瘤、食管癌和结直肠癌以及白血病细胞。相比之下,通过免疫组织化学染色或存活素mRNA表达的PCR分析,在相邻正常组织中均未检测到该蛋白。重要的是,存活素表达与肿瘤分级之间似乎存在正相关,并且提示切除或化疗后肿瘤复发。潜在地,这种蛋白可能会增加监测肿瘤患者的诊断和预后标志物种类。