Institute for Clinical & Experimental Surgery, University of Saarland, Homburg/Saar, Germany; Department of General, Visceral and Pediatric Surgery, University Medical Center, Georg August University, Göttingen, Germany.
J Surg Res. 2013 Dec;185(2):587-94. doi: 10.1016/j.jss.2013.06.005. Epub 2013 Jun 29.
Hepatic arterial infusion (HAI) of specific anti-tumor drugs can be more effective compared with systemic drug application. Herein, we studied whether HAI of temsirolimus is effective to inhibit tumor growth of colorectal liver metastases after liver resection.
Twenty-four Wistar Albino Glaxo from Rijswijk (WAG/Rij) rats were randomized to four groups and underwent subcapsular implantation of CC531 colorectal cancer cells in the left liver lobe. In two groups, a 70% liver resection (Phx) was performed simultaneously. After 10 d, animals received either a HAI of temsirolimus (CCI-779) or saline solution (controls). Tumor growth was determined on d 10 and 13 using three-dimensional ultrasound. On d 13, tumor tissue was removed for histologic and immunohistochemical analysis.
Sham controls revealed a tumor growth of ∼40% from d 10 to d 13. HAI of temsirolimus completely inhibited this tumor growth. Controls with Phx showed a tumor growth of >60%. In contrast, HAI of temsirolimus in Phx animals did not only inhibit tumor growth but was even capable of decreasing the tumor size by ∼8%. Immunohistochemical analysis of the tumors showed a decreased proliferation rate and an increased cleaved caspase-3 activity, which was associated with a significant reduction of platelet endothelial cell adhesion molecule (PECAM)-1-positive cells after HAI of temsirolimus.
HAI of temsirolimus inhibits tumor growth of CC531 colorectal liver metastases even if a growth-stimulating procedure like Phx is performed. Inhibition of tumor growth is provided by a decrease of tumor vascularization associated with an inhibition of tumor cell proliferation and an induction of tumor cell apoptosis.
与全身药物应用相比,肝动脉输注(HAI)特定的抗肿瘤药物可能更有效。在此,我们研究了肝切除术后 HAI 替西罗莫司是否能有效抑制结直肠肝转移的肿瘤生长。
24 只 Wistar Albino Glaxo from Rijswijk(WAG/Rij)大鼠随机分为四组,在左肝叶皮下植入 CC531 结直肠癌细胞。两组均同时行 70%肝切除术(Phx)。术后 10 d,动物分别接受替西罗莫司(CCI-779)HAI 或生理盐水(对照)治疗。第 10 天和第 13 天使用三维超声测量肿瘤生长情况。第 13 天,切除肿瘤组织进行组织学和免疫组化分析。
假手术对照显示,从第 10 天到第 13 天肿瘤生长约 40%。HAI 替西罗莫司完全抑制了这种肿瘤生长。Phx 对照组的肿瘤生长超过 60%。相比之下,Phx 动物中 HAI 替西罗莫司不仅抑制肿瘤生长,甚至能够使肿瘤体积缩小约 8%。肿瘤组织的免疫组化分析显示,增殖率降低,cleaved caspase-3 活性增加,这与 HAI 替西罗莫司后血小板内皮细胞黏附分子(PECAM)-1 阳性细胞显著减少有关。
即使进行 Phx 等促进生长的操作,HAI 替西罗莫司也能抑制 CC531 结直肠肝转移的肿瘤生长。肿瘤生长的抑制是通过降低与肿瘤细胞增殖抑制和肿瘤细胞凋亡诱导相关的肿瘤血管生成来实现的。