Debrock G, Vanhentenrijk V, Sciot R, Debiec-Rychter M, Oyen R, Van Oosterom A
Department of Medical Oncology, University Hospital Gasthuisberg, Universiteit Leuven, Herestraat 49, Leuven 3000, Belgium.
Br J Cancer. 2003 Oct 20;89(8):1409-12. doi: 10.1038/sj.bjc.6601306.
Agents of the thiazolidinedione drug family can terminally differentiate human liposarcoma cells in vitro by activating genes responsible for lipocyte differentiation. One study has shown clinical activity of troglitazone treatment in liposarcoma patients. We sought to find further evidence for this result. In all, 12 patients with a liposarcoma received rosiglitazone 4 mg b.d. They were followed clinically and with repeated biopsies for histological and biological studies. At the molecular level the mRNA translation of three genes that are induced by this treatment (peroxisome proliferator-activated receptor gamma (PPARgamma), adipsin and fatty acid binding protein) was determined. Nine patients were eligible for evaluation. One patient had to stop treatment due to hepatotoxicity. The mean time to progression was 6 months (2 - 16 months), with one patient still on treatment. We did not see any significant change in histologic appearance of the liposarcomas by the treatment. The level of gene expression changed significantly in two patients, but this did not result in a clinical response. Based on this study, rosiglitazone is not effective as an antitumoral drug in the treatment of liposarcomas. Increased PPARgamma activity does not correlate with the clinical evolution.
噻唑烷二酮类药物家族的药物可通过激活负责脂肪细胞分化的基因,在体外使人类脂肪肉瘤细胞终末分化。一项研究显示曲格列酮治疗脂肪肉瘤患者具有临床活性。我们试图为这一结果寻找更多证据。共有12例脂肪肉瘤患者接受罗格列酮每日两次、每次4毫克的治疗。对他们进行临床随访,并反复进行活检以进行组织学和生物学研究。在分子水平上,测定了这种治疗所诱导的三个基因(过氧化物酶体增殖物激活受体γ(PPARγ)、脂肪酶和脂肪酸结合蛋白)的mRNA翻译情况。九例患者符合评估条件。一名患者因肝毒性不得不停止治疗。平均进展时间为6个月(2至16个月),有一名患者仍在接受治疗。我们未观察到治疗使脂肪肉瘤的组织学外观有任何显著变化。两名患者的基因表达水平有显著改变,但这并未导致临床反应。基于这项研究,罗格列酮作为一种抗肿瘤药物在治疗脂肪肉瘤方面无效。PPARγ活性增加与临床进展无关。