Mirowski M, Rozalski M, Krajewska U, Hanausek M, Wierzbicki R
Department of Biochemistry, Medical University, Lodz, Poland.
Neoplasma. 1997;44(2):85-9.
We have tested the expression of a 65-kDa oncofetal protein (p65) after combined treatment with menadione and methotrexate in hamsters transplanted with Kirkman-Robins hepatoma. The treatment of tumor-bearing animals with these compounds significantly inhibited both the tumor development and the expression of p65. This inhibition in tumor tissue was calculated from densitograms of Western blots. The inhibition of p65 expression was also confirmed in the serum of hepatoma bearing animals by using solid-phase radioimmunoassay (RIA) to quantify the specificity of polyclonal antibodies to fetal p65 molecules. Additionally, p65 was shown to localize both in cytoplasm and in the nuclear extracts prepared from hepatoma tissue.
我们检测了在移植了柯克曼-罗宾斯肝癌的仓鼠中,维生素K3和甲氨蝶呤联合治疗后一种65千道尔顿癌胚蛋白(p65)的表达情况。用这些化合物处理荷瘤动物显著抑制了肿瘤发展和p65的表达。肿瘤组织中的这种抑制作用是根据蛋白质印迹法的光密度扫描图计算得出的。通过使用固相放射免疫测定法(RIA)来量化多克隆抗体对胎儿p65分子的特异性,荷瘤动物血清中p65表达的抑制也得到了证实。此外,p65在肝癌组织制备的细胞质和核提取物中均有定位。