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纳米工程化间充质干细胞向转移性乳腺癌细胞递送纳米颗粒

Nanoparticle delivery to metastatic breast cancer cells by nanoengineered mesenchymal stem cells.

作者信息

Saulite Liga, Pleiko Karlis, Popena Ineta, Dapkute Dominyka, Rotomskis Ricardas, Riekstina Una

机构信息

Faculty of Medicine, University of Latvia, Raina Blvd. 19, LV-1586 Riga, Latvia.

Biomedical Physics Laboratory, National Cancer Institute, P. Baublio Street 3b, LT-08406 Vilnius, Lithuania.

出版信息

Beilstein J Nanotechnol. 2018 Jan 29;9:321-332. doi: 10.3762/bjnano.9.32. eCollection 2018.

Abstract

We created a 3D cell co-culture model by combining nanoengineered mesenchymal stem cells (MSCs) with the metastatic breast cancer cell line MDA-MD-231 and primary breast cancer cell line MCF7 to explore the transfer of quantum dots (QDs) to cancer cells. First, the optimal conditions for high-content QD loading in MSCs were established. Then, QD uptake in breast cancer cells was assessed after 24 h in a 3D co-culture with nanoengineered MSCs. We found that incubation of MSCs with QDs in a serum-free medium provided the best accumulation results. It was found that 24 h post-labelling QDs were eliminated from MSCs. Our results demonstrate that breast cancer cells efficiently uptake QDs that are released from nanoengineered MSCs in a 3D co-culture. Moreover, the uptake is considerably enhanced in metastatic MDA-MB-231 cells compared with MCF7 primary breast cancer cells. Our findings suggest that nanoengineered MSCs could serve as a vehicle for targeted drug delivery to metastatic cancer.

摘要

我们通过将纳米工程化间充质干细胞(MSCs)与转移性乳腺癌细胞系MDA-MD-231和原发性乳腺癌细胞系MCF7相结合,创建了一个3D细胞共培养模型,以探索量子点(QDs)向癌细胞的转移。首先,确定了MSCs中高含量QD负载的最佳条件。然后,在与纳米工程化MSCs进行3D共培养24小时后,评估乳腺癌细胞对QD的摄取情况。我们发现,在无血清培养基中用QD孵育MSCs可提供最佳的积累结果。结果发现,标记后24小时,QD从MSCs中被清除。我们的结果表明,在3D共培养中,乳腺癌细胞能有效摄取从纳米工程化MSCs释放的QD。此外,与MCF7原发性乳腺癌细胞相比,转移性MDA-MB-231细胞中的摄取显著增强。我们的研究结果表明,纳米工程化MSCs可作为向转移性癌症进行靶向药物递送的载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7644/5815277/c3a999f957c3/Beilstein_J_Nanotechnol-09-321-g002.jpg

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