Tamoxifen Citrate- loaded synthetic high-density lipoproteins: Assessment of cellular toxicity in breast cancer cells

Ameerah A. Radhi, Wedad K. Ali, Fitua Al-Saedi
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Abstract

Tamoxifen Citrate (TC) is the standard endocrine therapy for estrogen receptor (ER) positive breast cancer. TC is a selective estrogen receptor modulator (SERM) whose estrogenic properties in uterus have been linked to increased side effects like blood clots, endometrial polyps and cancer. Therefore, significant amount of research has been carried out to develop tamoxifen loaded nano-formulations with a preferential accumulation in tumor tissue rather than healthy tissues. Synthetic high-density lipoproteins (sHDL) are novel nanocarriers with inherent active-targeting ability towards tumor cells through the ligand–receptor interaction between apolipoprotein A-I (Apo A-I) and scavenger receptor class B type I (SR-BI) overexpressed in various malignant cells. The current study was carried out to investigate whether encapsulation of TC in sHDL could improve the cytotoxic effect of TC against malignant cells. For this purpose, the cytotoxicity of TC-sHDL was evaluated in MCF-7 cell line in vitro. MTT assay demonstrated the increased cytotoxicity of TC-sHDL against cancer cells as compared with the cytotoxic effect of the free drug.
负载柠檬酸他莫昔芬的合成高密度脂蛋白:乳腺癌细胞毒性的评估
柠檬酸他莫昔芬(TC)是雌激素受体(ER)阳性乳腺癌的标准内分泌治疗药物。TC是一种选择性雌激素受体调节剂(SERM),其在子宫中的雌激素特性与血凝块、子宫内膜息肉和癌症等副作用增加有关。因此,人们进行了大量的研究,以开发负载他莫昔芬的纳米配方,使其优先在肿瘤组织而不是健康组织中积累。合成高密度脂蛋白(sHDL)是一种新型纳米载体,通过载脂蛋白A-I (Apo A-I)与各种恶性细胞中过表达的清道夫受体B类I型(SR-BI)之间的配体-受体相互作用,具有固有的靶向肿瘤细胞的活性。本研究旨在探讨sHDL包封TC是否能提高TC对恶性细胞的细胞毒作用。为此,我们在体外对MCF-7细胞株进行了细胞毒性评价。MTT试验表明,与游离药物相比,TC-sHDL对癌细胞的细胞毒性增加。
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