Division of Pharmaceutics, College of Pharmacy, The Ohio State University, 500 West 12th Avenue, Columbus, Ohio 43210, USA.
Pharm Res. 2011 Dec;28(12):3256-64. doi: 10.1007/s11095-011-0498-2. Epub 2011 Jun 28.
We have demonstrated that (-)-gossypol-enriched cottonseed oil [(-)-GPCSO] can down-regulate Bcl-2 expression in MCF-7 and primary cultured human breast cancer epithelial cells (PCHBCECs). However, this agent has not been evaluated in vivo due to its limited solubility. We aimed to develop liposomes containing (-)-GPCSO to suppress Bcl-2/Bcl-xL expression.
(-)-GPCSO liposomes were prepared and evaluated for effects on breast cancer cell viability, MDA-MB-231 xenograft tumor growth, cellular Bcl-2 and Bcl-xL mRNA levels, and chemosensitivity to paclitaxel.
(-)-GPCSO liposomes prepared had excellent stability. Cytotoxicity of (-)-GPCSO liposomes was significantly reduced compared to (-)-GPCSO in culture medium. Bcl-2 and Bcl-xL mRNA expression was down-regulated by (-)-GPCSO in culture medium or (-)-GPCSO liposomes in MDA-MB-231 cells. In PCHBCECs, Bcl-2 and Bcl-xL expression were down-regulated by (-)-GPCSO liposomes. (-)-GPCSO in culture medium induced only a mild reduction in Bcl-xL. In the MDA-MB-231 xenograft tumor model, (-)-GPCSO liposomes exhibited tumor-suppressive activity and significantly reduced intratumoral Bcl-2 and Bcl-xL expression. Cytotoxicity of paclitaxel was increased by pretreatment with (-)-GPCSO liposomes in MDA-MB-231 and PCHBCECs.
Findings suggest that (-)-GPCSO liposomes warrant continued investigation as a chemosensitizer for breast cancers exhibiting Bcl-2-/Bcl-xL-mediated drug resistance.
我们已经证明,(-)-棉酚富集棉籽油[(-)-GPCSO]可以下调 MCF-7 和原代培养的人乳腺癌上皮细胞(PCHBCECs)中的 Bcl-2 表达。然而,由于其溶解度有限,该药物尚未在体内进行评估。我们旨在开发含有(-)-GPCSO 的脂质体来抑制 Bcl-2/Bcl-xL 的表达。
制备(-)-GPCSO 脂质体并评估其对乳腺癌细胞活力、MDA-MB-231 异种移植肿瘤生长、细胞 Bcl-2 和 Bcl-xL mRNA 水平以及紫杉醇化疗敏感性的影响。
制备的(-)-GPCSO 脂质体具有优异的稳定性。与培养基中的(-)-GPCSO 相比,(-)-GPCSO 脂质体的细胞毒性显著降低。(-)-GPCSO 在培养基或(-)-GPCSO 脂质体中均可下调 MDA-MB-231 细胞中的 Bcl-2 和 Bcl-xL mRNA 表达。在 PCHBCECs 中,(-)-GPCSO 脂质体下调 Bcl-2 和 Bcl-xL 的表达。培养基中的(-)-GPCSO 仅诱导 Bcl-xL 轻度减少。在 MDA-MB-231 异种移植肿瘤模型中,(-)-GPCSO 脂质体表现出肿瘤抑制活性,并显著降低肿瘤内 Bcl-2 和 Bcl-xL 的表达。在 MDA-MB-231 和 PCHBCECs 中,用(-)-GPCSO 脂质体预处理可增加紫杉醇的细胞毒性。
研究结果表明,(-)-GPCSO 脂质体作为 Bcl-2-/Bcl-xL 介导的耐药性乳腺癌的化疗增敏剂值得进一步研究。