Mechanical Engineering Department, Texas Tech University, Lubbock, TX 79409, USA.
Int J Mol Sci. 2024 May 14;25(10):5348. doi: 10.3390/ijms25105348.
Metastasis in breast cancer is the major cause of death in females (about 30%). Based on our earlier observation that Vitamin D3 downregulates mTOR, we hypothesized that Vitamin D3 conjugated to gold nanoparticles (VD3-GNPs) reduces breast cancer aggressiveness by downregulating the key cancer controller PI3K/AKT/mTOR. Western blots, migration/invasion assays, and other cell-based, biophysical, and bioinformatics studies are used to study breast cancer cell aggressiveness and nanoparticle characterization. Our VD3-GNP treatment of breast cancer cells (MCF-7 and MDA-MB-231) significantly reduces the aggressiveness (cancer cell migration and invasion rates > 45%) via the simultaneous downregulation of ETV7 and the Hippo pathway. Consistent with our hypothesis, we, indeed, found a downregulation of the PI3K/AKT/mTOR pathway. It is surprising that the extremely low dose of VD3 in the nano formulation (three orders of magnitude lower than in earlier studies) is quite effective in the alteration of cancer invasiveness and cell signaling pathways. Clearly, VD3-GNPs are a viable candidate for non-toxic, low-cost treatment for reducing breast cancer aggressiveness.
乳腺癌转移是女性死亡的主要原因(约 30%)。基于我们之前观察到维生素 D3 下调 mTOR,我们假设将维生素 D3 与金纳米粒子(VD3-GNPs)结合可以通过下调关键的癌症控制器 PI3K/AKT/mTOR 来降低乳腺癌的侵袭性。我们使用 Western blot、迁移/侵袭测定以及其他基于细胞的、生物物理和生物信息学研究来研究乳腺癌细胞的侵袭性和纳米粒子的特性。我们用 VD3-GNP 处理乳腺癌细胞(MCF-7 和 MDA-MB-231),通过同时下调 ETV7 和 Hippo 通路,显著降低了侵袭性(癌细胞迁移和侵袭率>45%)。与我们的假设一致,我们确实发现 PI3K/AKT/mTOR 通路被下调。令人惊讶的是,纳米制剂中维生素 D3 的极低剂量(比早期研究低三个数量级)在改变癌症侵袭性和细胞信号通路方面非常有效。显然,VD3-GNPs 是一种可行的候选物,可用于非毒性、低成本治疗,以降低乳腺癌的侵袭性。