Helen F. Graham Cancer Center & Research Institute , Newark, Delaware 19713, United States.
ACS Nano. 2016 Dec 27;10(12):10631-10635. doi: 10.1021/acsnano.6b07673. Epub 2016 Dec 1.
Gold nanoparticles have received much attention recently as carriers for anticancer drugs and therapeutic oligonucleotides, but little research has investigated their potential to act as stand-alone therapeutics. Previous studies interrogating their short- and long-term systemic toxicity have found that although gold nanoparticles accumulate within and clear slowly from the liver and spleen, they do not appear to exert toxic effects in these organs. Interestingly, gold nanoparticles innately exhibit the ability to modulate the tumor microenvironment specifically by interfering with crosstalk between tumor cells and stromal cells. In this issue of ACS Nano, Mukherjee and colleagues demonstrate that bare gold nanoparticles can disturb crosstalk between pancreatic stellate cells and pancreatic cancer cells by modulating the cellular secretome to reduce the growth of desmoplastic tissue and inhibit tumor growth. In this Perspective, we highlight opportunities for anticancer targeting within the tumor microenvironment and discuss gold nanoparticles as potential mediators of microenvironment-targeted therapy.
金纳米颗粒作为抗癌药物和治疗性寡核苷酸的载体受到了广泛关注,但很少有研究探讨其作为独立治疗剂的潜力。以前的研究调查了它们的短期和长期系统毒性,发现尽管金纳米颗粒在肝脏和脾脏中积累并缓慢清除,但它们似乎没有在这些器官中产生毒性作用。有趣的是,金纳米颗粒天生就具有调节肿瘤微环境的能力,特别是通过干扰肿瘤细胞和基质细胞之间的串扰。在本期 ACS Nano 杂志上,Mukherjee 及其同事证明,裸金纳米颗粒可以通过调节细胞分泌组来减少纤维组织的生长并抑制肿瘤生长,从而干扰胰腺星状细胞和胰腺癌细胞之间的串扰。在这篇观点文章中,我们强调了在肿瘤微环境中进行抗癌靶向治疗的机会,并讨论了金纳米颗粒作为微环境靶向治疗的潜在介质。