Department of Anatomy II: Experimental Morphology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Oncol Res. 2010;18(8):387-93. doi: 10.3727/096504010x12644422320708.
Rosiglitazone, a peroxisome proliferator activated receptor-gamma (PPAR-gamma) agonist used in clinical practice to treat type 2 diabetes, has been shown to inhibit neuroblastoma cell proliferation in vitro. In the present study, SK-N-SH neuroblastoma cells were subcutaneously injected into SCID mice and their growth and metastatic behavior under the treatment with rosiglitazone was analyzed. Therapeutic effects were evaluated comparing primary tumor weight, cell proliferation, apoptosis, and number of pulmonary metastasis. Rosiglitazone significantly decreased cell proliferation of the SK-N-SH neuroblastomas from 57.0% in the solvent control to 45.0% and 47.0% in the two treatment groups, respectively. However, primary tumor weight, apoptosis, and metastasis were not considerably influenced. These results indicate that the PPAR-gamma agonist rosiglitazone has only slight antitumor effects on SK-N-SH neuroblastoma growth in vivo in contrast to in vitro.
罗格列酮,一种临床上用于治疗 2 型糖尿病的过氧化物酶体增殖物激活受体-γ(PPAR-γ)激动剂,已被证明可抑制体外神经母细胞瘤细胞的增殖。在本研究中,将 SK-N-SH 神经母细胞瘤细胞皮下注射到 SCID 小鼠中,并分析罗格列酮处理下它们的生长和转移行为。通过比较原发性肿瘤重量、细胞增殖、凋亡和肺转移的数量来评估治疗效果。罗格列酮显著降低了 SK-N-SH 神经母细胞瘤的细胞增殖,从溶剂对照组的 57.0%分别降至两个治疗组的 45.0%和 47.0%。然而,原发性肿瘤重量、凋亡和转移并没有受到明显影响。这些结果表明,与体外相比,PPAR-γ 激动剂罗格列酮对 SK-N-SH 神经母细胞瘤在体内的生长仅有轻微的抗肿瘤作用。