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一种新型水溶性棉酚衍生物可提高结肠癌化疗敏感性并促进生长抑制。

A novel water-soluble gossypol derivative increases chemotherapeutic sensitivity and promotes growth inhibition in colon cancer.

机构信息

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.

出版信息

J Med Chem. 2010 Aug 12;53(15):5502-10. doi: 10.1021/jm1001698.

Abstract

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.

摘要

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。

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