Witty J P, Jensen R A, Johnson A L
Department of Biological Sciences, University of Notre Dame, IN 46556, USA.
Anticancer Res. 1998 Mar-Apr;18(2B):1223-30.
Interactions between Bcl-2 and its related proteins regulate cell death in a number of tissues including the ovary. Some Bcl-2-related proteins (Bcl-2, Bcl-xLong, MCl-1, and Dad-1) function as cell death repressors, whereas others (Bax, Bcl-xShort, Bak, and Bad) facilitate apoptosis.
Immunoblotting and immunohistochemistry using specific antisera were performed with a panel of human ovarian carcinomas and normal human ovaries.
All Bcl-2 related proteins were expressed in normal and malignant ovarian tissues. Higher levels of Bcl-2 versus Bcl-xLong were observed in normal ovary by immunoblotting, compared to a majority of cancer samples. Increased levels of death-inducing Bax were related to malignant transformation across all types of ovarian cancer included in this study.
The results provide further evidence that a balance of expression among Bcl-2 family members may regulate ovarian cancer cell survival.
Bcl-2与其相关蛋白之间的相互作用在包括卵巢在内的多种组织中调节细胞死亡。一些Bcl-2相关蛋白(Bcl-2、Bcl-xL、Mcl-1和Dad-1)发挥细胞死亡抑制因子的作用,而其他蛋白(Bax、Bcl-xS、Bak和Bad)则促进细胞凋亡。
使用特异性抗血清对一组人卵巢癌和正常人类卵巢进行免疫印迹和免疫组织化学检测。
所有Bcl-2相关蛋白均在正常和恶性卵巢组织中表达。通过免疫印迹法观察到,与大多数癌症样本相比,正常卵巢中Bcl-2的水平高于Bcl-xL。在本研究纳入的所有类型卵巢癌中,诱导死亡的Bax水平升高与恶性转化有关。
这些结果进一步证明,Bcl-2家族成员之间表达的平衡可能调节卵巢癌细胞的存活。