Gabor F, Haberl I, Wirth M, Richter K, Theyer G, Baumgartner G, Wenzl E, Hamilton G
SALZBURG UNIV,SCH MED,DEPT SURG,A-5020 SALZBURG,AUSTRIA. SALZBURG UNIV,INST BIOCHEM,A-5020 SALZBURG,AUSTRIA. KH LAINZ,LUDWIG BOLTZMANN INST CLIN ONCOL,VIENNA,AUSTRIA.
Int J Oncol. 1996 Sep;9(3):527-31. doi: 10.3892/ijo.9.3.527.
The pseudoautosomal encoded MIC2 glycoprotein is a tumor-associated antigen of Ewing's sarcoma (ES) and closely related tumors of unknown function. To investigate the use of this protein as selective drug carrier recombinant MIC2 was coupled to doxorubicin by a two step glutaraldehyde method (molar ratio DOX/MIC2 of 32 and 16). The conjugates showed dose-dependent cytostatic activity against the ES cell line SK-ES1, the peripheral neuroectodermal line KAL and the prostate cancer cell line PC-3 concurrent with reduced toxicity against normal lymphoblasts. In comparison to free doxorubicin the MIC2-doxorubicin conjugates exhibited highest activity against the PC-3 cell line. Confocal microscopy showed intracellular accumulation of MIC2 conjugates.
假常染色体编码的MIC2糖蛋白是尤因肉瘤(ES)及功能未知的密切相关肿瘤的肿瘤相关抗原。为研究该蛋白作为选择性药物载体的用途,通过两步戊二醛法(阿霉素与MIC2的摩尔比为32和16)将重组MIC2与阿霉素偶联。这些偶联物对ES细胞系SK-ES1、外周神经外胚层系KAL和前列腺癌细胞系PC-3显示出剂量依赖性的细胞生长抑制活性,同时对正常淋巴细胞的毒性降低。与游离阿霉素相比,MIC2-阿霉素偶联物对PC-3细胞系表现出最高活性。共聚焦显微镜显示MIC2偶联物在细胞内积聚。