Sharma Pankaj, Perez Diego, Cabrera Armando, Rosas Noe, Arias Jose Luis
Instituto De Química, UNAM Circuito Exterior, Coyoacan México DF.04510, Mexico.
Acta Pharmacol Sin. 2008 Aug;29(8):881-90. doi: 10.1111/j.1745-7254.2008.00818.x.
Antimony, a natural element that has been used as a drug for over more than 100 years, has remarkable therapeutic efficacy in patients with acute promyelocytic leukemia. This review focuses on recent advances in developing antimony anticancer agents with an emphasis on antimony coordination complexes, Sb (III) and Sb (V). These complexes, which include many organometallic complexes, may provide a broader spectrum of antitumoral activity. They were compared with classical platinum anticancer drugs. The review covers the literature data published up to 2007. A number of antimonials with different antitumoral activities are known and have diverse applications, even though little research has been done on their possibilities. It might be feasible to develop more specific and effective inhibitors for phosphatase-targeted, anticancer therapeutics through the screening of sodium stibogluconate (SSG) and potassium antimonyltartrate-related compounds, which are comprised of antimony conjugated to different organic moieties. For example, SSG appears to be a better inhibitor than suramin which is a compound known for its antineoplastic activity against several types of cancers.
锑是一种天然元素,用作药物已有100多年历史,对急性早幼粒细胞白血病患者具有显著的治疗效果。本综述重点关注锑类抗癌药物的最新进展,重点是锑配位络合物、Sb(III)和Sb(V)。这些络合物,包括许多有机金属络合物,可能具有更广泛的抗肿瘤活性。将它们与经典的铂类抗癌药物进行了比较。本综述涵盖了截至2007年发表的文献数据。已知有多种具有不同抗肿瘤活性的锑剂,其应用也多种多样,尽管对其潜力的研究较少。通过筛选葡糖酸锑钠(SSG)和酒石酸锑钾相关化合物(它们由与不同有机部分共轭的锑组成),开发针对磷酸酶的更特异性和有效的抗癌治疗抑制剂可能是可行的。例如,SSG似乎比苏拉明(一种以对几种癌症具有抗肿瘤活性而闻名的化合物)是更好的抑制剂。