Schumacher Guido, Oidtmann Marijke, Rueggeberg Anne, Jacob Dietmar, Jonas Sven, Langrehr Jan-M, Neuhaus Ruth, Bahra Marcus, Neuhaus Peter
Department of General, Visceral, and Transplantation Surgery, Charite Campus Virchow Klinikum, Humboldt University, Augustenburger Platz 1, Berlin 13353, Germany.
World J Gastroenterol. 2005 Mar 14;11(10):1420-5. doi: 10.3748/wjg.v11.i10.1420.
Standard immunosuppression after organ transplantation stimulates tumor growth. Sirolimus has a strong antiproliferative and a tumor inhibiting effect. The purpose is to assess the effect on tumor growth of the immuno-suppressive compounds sirolimus and tacrolimus alone and in combination on cells of human hepatocellular carcinoma.
We used the human cell lines SK-Hep 1 and Hep 3B derived from hepatocellular carcinoma. Proliferation analyses after treatment with sirolimus, tacrolimus, or the combination of both were performed. FACS analyses were done to reveal cell cycle changes and apoptotic cell death. The expression of apoptosis-related proteins was estimated by Western blots.
Sirolimus alone or combined with tacrolimus inhibited the growth of both cell lines after 5 d by up to 35% in SK-Hep 1 cells, and by up to 68% in Hep 3B cells at 25 ng/mL. Tacrolimus alone stimulated the growth by 12% after 5 ng/mL and by 25% after 25 ng/mL in Hep 3B cells. We found an increase of apoptotic Hep 3B cells from 6 to 16%, and a G1-arrest in SK-Hep 1 cells with an increase of cells from 61 to 82%, when sirolimus and tacrolimus were combined. Bcl-2 was down-regulated in Hep 3B, but not in SK-Hep 1 cells after combined treatment.
Sirolimus appears to inhibit the growth of hepatocellular carcinoma cells alone and in combination with tacrolimus. Sirolimus seems to inhibit the growth stimulation of tacrolimus.
器官移植后的标准免疫抑制会刺激肿瘤生长。西罗莫司具有强大的抗增殖和肿瘤抑制作用。本研究旨在评估免疫抑制化合物西罗莫司和他克莫司单独及联合使用对人肝癌细胞肿瘤生长的影响。
我们使用了源自肝细胞癌的人细胞系SK-Hep 1和Hep 3B。在用西罗莫司、他克莫司或两者联合处理后进行增殖分析。通过流式细胞术分析揭示细胞周期变化和凋亡性细胞死亡。通过蛋白质免疫印迹法评估凋亡相关蛋白的表达。
单独使用西罗莫司或与他克莫司联合使用,5天后两种细胞系的生长均受到抑制,在SK-Hep 1细胞中抑制率高达35%,在Hep 3B细胞中,25 ng/mL时抑制率高达68%。单独使用他克莫司时,在Hep 3B细胞中,5 ng/mL处理5天后细胞生长刺激了12%,25 ng/mL处理后刺激了25%。当西罗莫司和他克莫司联合使用时,我们发现Hep 3B细胞的凋亡率从6%增加到16%,SK-Hep 1细胞出现G1期阻滞,细胞比例从61%增加到82%。联合处理后,Hep 3B细胞中的Bcl-2表达下调,但SK-Hep 1细胞中未下调。
西罗莫司单独及与他克莫司联合使用似乎均可抑制肝癌细胞的生长。西罗莫司似乎可抑制他克莫司的生长刺激作用。