Umeda Y, Tsuruo T, Mori S, Arimori S, Sugawara I
Department of Internal Medicine, School of Medicine, Tokai University, Kanagawa, Japan.
Tokai J Exp Clin Med. 1990 May;15(2-3):179-87.
Acquired resistance developed after chemotherapy is characterized by lower sensitivity to anticancer agents. We utilized two monoclonal antibodies (MABs): MRK16 which recognized 170 to 180 kD P-glycoprotein and MRK20 which recognized 85 kD protein, to investigate the frequency of multidrug-resistant cancer cells appearing during treatment of 23 cases of leukemias and 27 cases of malignant lymphomas. The reactivities of these MABs with lymphocytes and blastic cells were examined by flow cytometry and immunocytochemistry. The following findings were obtained. First, among 50 cases, increases in MRK16-reactive cells and MRK20-reactive cells were noted in 17 cases (34%) and 28 cases (56%), respectively. Second, the increase of MRK16-positive cells in three cases and the increase of MRK20-positive cells in two cases were correlated with dosages of the corresponding anticancer drugs used. Although we investigated the total amounts of anti-cancer drugs used, we were not able to detect exactly when P-glycoprotein recognized by MRK16 and the 85 kDa protein recognized by MRK20 appeared in these resistant cells during treatment. More cases will be required to investigate the significance between treatment and reactivity of MRK16 or MRK20 with leukemia or lymphomas cells.
化疗后产生的获得性耐药表现为对抗癌药物的敏感性降低。我们使用了两种单克隆抗体(MABs):识别170至180 kD P-糖蛋白的MRK16和识别85 kD蛋白的MRK20,以研究23例白血病和27例恶性淋巴瘤治疗期间出现的多药耐药癌细胞的频率。通过流式细胞术和免疫细胞化学检测这些MABs与淋巴细胞和母细胞的反应性。获得了以下结果。首先,在50例病例中,MRK16反应性细胞增加的有17例(34%),MRK20反应性细胞增加的有28例(56%)。其次,3例MRK16阳性细胞的增加和2例MRK20阳性细胞的增加与所用相应抗癌药物的剂量相关。虽然我们调查了所用抗癌药物的总量,但我们无法确切检测出在治疗期间MRK16识别的P-糖蛋白和MRK20识别的85 kDa蛋白是何时出现在这些耐药细胞中的。需要更多病例来研究MRK16或MRK20与白血病或淋巴瘤细胞的治疗和反应性之间的关系。