NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore , Singapore 117456, Singapore.
Centre for Advanced 2D Materials and Graphene Research Centre, National University of Singapore , Singapore 117546, Singapore.
ACS Nano. 2016 Mar 22;10(3):3424-34. doi: 10.1021/acsnano.5b07409. Epub 2016 Mar 7.
Graphene nanomaterials have been actively investigated for biomedical and biological applications, including that of cancer. Despite progress made, most of such studies are conducted on dispersed graphene nanosheets in solution. Consequently, the use of planar graphene films, especially in cancer research, has not been fully explored. Here, we investigate the cellular interactions between the graphene material films and breast cancer cell lines, specifically the effects these films have on cellular proliferation, spreading area, and cytotoxicity. We demonstrate that the graphene oxide (GO) film selectively accelerates the proliferation of both metastatic (MDA-MB-231) and nonmetastatic (MCF-7) breast cancer cells, but not that of noncancer breast epithelial cells (MCF-10A). Contrastingly, this accelerated proliferation is not observed with the use of graphene (G) film. Moreover, GO induces negligible cytotoxicity on these cells. We suggest that the observed phenomena originate from the synergistic effect resulted from the high loading capacity and conformational change of cellular attachment proteins on the GO film, and the high amount of oxygenated groups present in the material. We anticipate that our findings can further shed light on the graphene-cancer cellular interactions and provide better understanding for the future design and application of graphene-based nanomaterials in cancer research.
石墨烯纳米材料在生物医学和生物学应用中得到了广泛的研究,包括癌症。尽管已经取得了进展,但大多数此类研究都是在溶液中分散的石墨烯纳米片中进行的。因此,平面石墨烯薄膜的应用,特别是在癌症研究中的应用,尚未得到充分探索。在这里,我们研究了石墨烯材料薄膜与乳腺癌细胞系之间的细胞相互作用,特别是这些薄膜对细胞增殖、扩散面积和细胞毒性的影响。我们证明氧化石墨烯(GO)薄膜选择性地加速了转移性(MDA-MB-231)和非转移性(MCF-7)乳腺癌细胞的增殖,但不能加速非癌细胞乳腺癌上皮细胞(MCF-10A)的增殖。相比之下,使用石墨烯(G)薄膜则不会观察到这种加速增殖现象。此外,GO 对这些细胞的细胞毒性可以忽略不计。我们认为,观察到的现象源于高载药能力和细胞附着蛋白构象变化与材料中存在大量含氧基团之间的协同作用。我们期望我们的发现可以进一步阐明石墨烯与癌症的细胞相互作用,并为未来基于石墨烯的纳米材料在癌症研究中的设计和应用提供更好的理解。