Rupertus Kathrin, Senger Sebastian, Menger Michael D, Schilling Martin K, Kollmar Otto
Department of General, Visceral, Vascular and Pediatric Surgery, University of Saarland, Homburg/Saar, Germany.
J Surg Res. 2012 Aug;176(2):517-23. doi: 10.1016/j.jss.2011.09.062. Epub 2011 Oct 25.
The erythropoietin-analogue darbepoetin-α (DPO) improves liver function and regeneration after hepatectomy (Phx), however, also enhances Phx-induced tumor cell engraftment and neovascularization. Because it is unknown whether DPO also enhances the growth of established tumors, we herein studied the effect of DPO on established colorectal liver metastases after Phx.
CT26.WT cells were implanted into the liver of BALB/c mice. Five days after tumor establishment, animals underwent 50% Phx and received 10 μg/kgBW DPO or saline. Non-Phx animals with DPO or saline-treatment served as controls. Seven days after Phx tumors were analyzed regarding blood vessel formation, leukocyte adhesion, cell proliferation, apoptotic cell death, and growth using intravital fluorescence microscopy, histology, and immunohistochemistry.
The growth of established colorectal liver metastases was slightly stimulated after DPO-treatment in hepatectomized and non-hepatectomized animals. However, tumor vessel formation and tumor cell proliferation were significantly enhanced after DPO-treatment in hepatectomized and non-hepatectomized mice compared with controls. Apoptotic cell death and leukocyte-endothelial cell interaction were significantly reduced after DPO-treatment.
Our study indicates that DPO-treatment promotes neovascularization and cell proliferation in established colorectal liver metastases of hepatectomized and non-hepatectomized mice. DPO-application in patients with colorectal liver metastases might promote tumor progression and should therefore be avoided.
促红细胞生成素类似物达贝泊汀-α(DPO)可改善肝切除术后(Phx)的肝功能和肝脏再生,但也会增强Phx诱导的肿瘤细胞植入和新生血管形成。由于尚不清楚DPO是否也会促进已形成肿瘤的生长,我们在此研究了DPO对Phx术后已形成的结直肠癌肝转移灶的影响。
将CT26.WT细胞植入BALB/c小鼠肝脏。肿瘤形成5天后,动物接受50%肝切除术,并接受10μg/kg体重的DPO或生理盐水。接受DPO或生理盐水治疗的未进行肝切除术的动物作为对照。肝切除术后7天,使用活体荧光显微镜、组织学和免疫组织化学分析肿瘤的血管形成、白细胞黏附、细胞增殖、凋亡性细胞死亡和生长情况。
在肝切除和未肝切除的动物中,DPO治疗后已形成的结直肠癌肝转移灶的生长略有促进。然而,与对照组相比,肝切除和未肝切除的小鼠在DPO治疗后肿瘤血管形成和肿瘤细胞增殖显著增强。DPO治疗后凋亡性细胞死亡和白细胞-内皮细胞相互作用显著减少。
我们的研究表明,DPO治疗可促进肝切除和未肝切除小鼠已形成的结直肠癌肝转移灶的新生血管形成和细胞增殖。在结直肠癌肝转移患者中应用DPO可能会促进肿瘤进展,因此应避免使用。