Schadendorf Dirk
Department of Dermatology, Venerology, and Allergology, University Hospital Essen, Essen, Germany.
J Invest Dermatol. 2009 May;129(5):1061-3. doi: 10.1038/jid.2009.56.
Accumulating evidence suggests that peroxisome proliferator-activated receptor-gamma (PPARgamma)-binding ligands, currently used to treat diabetes, could be used to treat melanoma. Dissociation of their effects on apoptosis from pharmacological activity (i.e., PPARgamma activation) provides a molecular basis for exploiting these compounds to develop molecularly targeted anticancer agents. In this issue, Botton and co-workers demonstrate in vitro and in vivo antimelanoma effects of ciglitazone, a synthetic ligand-activating PPARgamma.
越来越多的证据表明,目前用于治疗糖尿病的过氧化物酶体增殖物激活受体γ(PPARγ)结合配体可用于治疗黑色素瘤。将它们对细胞凋亡的作用与药理活性(即PPARγ激活)分离,为利用这些化合物开发分子靶向抗癌药物提供了分子基础。在本期中,博顿及其同事证明了吡格列酮(一种激活PPARγ的合成配体)在体外和体内的抗黑色素瘤作用。