Tontonoz P, Singer S, Forman B M, Sarraf P, Fletcher J A, Fletcher C D, Brun R P, Mueller E, Altiok S, Oppenheim H, Evans R M, Spiegelman B M
Dana-Farber Cancer Institute, Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 1997 Jan 7;94(1):237-41. doi: 10.1073/pnas.94.1.237.
Induction of terminal differentiation represents a promising therapeutic approach to certain human malignancies. The peroxisome proliferator-activated receptor gamma (PPAR gamma) and the retinoid X receptor alpha (RXR alpha) form a heterodimeric complex that functions as a central regulator of adipocyte differentiation. Natural and synthetic ligands for both receptors have been identified. We demonstrate here that PPAR gamma is expressed at high levels in each of the major histologic types of human liposarcoma. Moreover, primary human liposarcoma cells can be induced to undergo terminal differentiation by treatment with the PPAR gamma ligand pioglitazone, suggesting that the differentiation block in these cells can be overcome by maximal activation of the PPAR pathway. We further demonstrate that RXR-specific ligands are also potent adipogenic agents in cells expressing the PPAR gamma/RXR alpha heterodimer, and that simultaneous treatment of liposarcoma cells with both PPAR gamma- and RXR-specific ligands results in an additive stimulation of differentiation. Liposarcoma cell differentiation is characterized by accumulation of intracellular lipid, induction of adipocyte-specific genes, and withdrawal from the cell cycle. These results suggest that PPAR gamma ligands such as thiazolidinediones and RXR-specific retinoids may be useful therapeutic agents for the treatment of liposarcoma.
诱导终末分化是治疗某些人类恶性肿瘤的一种有前景的方法。过氧化物酶体增殖物激活受体γ(PPARγ)和视黄酸X受体α(RXRα)形成一种异二聚体复合物,作为脂肪细胞分化的核心调节因子发挥作用。已经鉴定出这两种受体的天然和合成配体。我们在此证明,PPARγ在人类脂肪肉瘤的每种主要组织学类型中均高表达。此外,用PPARγ配体吡格列酮处理可诱导原代人脂肪肉瘤细胞发生终末分化,这表明通过最大程度激活PPAR途径可以克服这些细胞中的分化阻滞。我们进一步证明,RXR特异性配体在表达PPARγ/RXRα异二聚体的细胞中也是有效的脂肪生成剂,并且用PPARγ特异性配体和RXR特异性配体同时处理脂肪肉瘤细胞会导致分化的累加刺激。脂肪肉瘤细胞分化的特征是细胞内脂质积累、脂肪细胞特异性基因的诱导以及退出细胞周期。这些结果表明,噻唑烷二酮类等PPARγ配体和RXR特异性类视黄醇可能是治疗脂肪肉瘤的有用治疗药物。