Laboratory of Targeted Cancer Therapy, Institute of Health Sciences, Shanghai Institutes for Biological Sciences of Chinese Academy of Sciences & Shanghai Jiao-Tong University School of Medicine (SJTU-SM), Shanghai 200025, China.
J Med Chem. 2010 Aug 12;53(15):5502-10. doi: 10.1021/jm1001698.
Compound 1 ((-)-gossypol) has been long known as a chemical anticancer agent. With its low water solubility and toxicity, it is not widely used as a commercial drug. To overcome these disadvantages, several novel derivatives of gossypol were designed, synthesized, and analyzed. One of the derivatives, compound 7 (6-aminopenicillanic acid sodium-gossypolone), was identified with great water solubility and anticancer property, suggested by inducing a dramatically decrease in Bcl-2 and Bcl-xL protein expression level found in vitro and growth inhibition of murine colon tumor in vivo. Furthermore, it was also recognized with less toxicity than compound 1 in vivo and significantly increased chemotherapeutic sensitivity against colon cancer in combination with traditional chemotherapeutic agent 5-fluorouracil. Therefore, it is concluded that compound 7 is superior to parent compound 1, and further preclinical studies of compound 7 is necessary for colon cancer therapy.
化合物 1((-)-gossypol) 一直以来都被认为是一种化学抗癌剂。由于其水溶性低和毒性,它并没有被广泛用作商业药物。为了克服这些缺点,设计、合成并分析了几种新型的 gossypol 衍生物。其中一种衍生物,化合物 7(6-氨基青霉烷酸钠-gossypolone),具有很好的水溶性和抗癌特性,体外实验结果表明其能显著降低 Bcl-2 和 Bcl-xL 蛋白的表达水平,体内实验结果表明其对鼠结肠肿瘤的生长有抑制作用。此外,与母体化合物 1 相比,化合物 7 的体内毒性也较低,并且与传统化疗药物 5-氟尿嘧啶联合使用时,显著增加了对结肠癌的化疗敏感性。因此,化合物 7 优于母体化合物 1,有必要对化合物 7 进行进一步的临床前研究,以用于结肠癌的治疗。