Targeted photothermal ablation of murine melanomas with melanocyte-stimulating hormone analog-conjugated hollow gold nanospheres.
Lu. Wei W; Xiong. Chiyi C; Zhang. Guodong G; Huang. Qian Q; Zhang. Rui R; Zhang. Jin Z JZ; Li. Chun C
Key Findings
- MSH‑analog‑coated gold nanospheres specifically bind to melanoma cells via the MC1R receptor
- Targeted particles accumulate in tumors and are taken up by cells through receptor‑mediated endocytosis
- Low‑dose infrared laser (30 J/cm²) successfully ablates tumors in mice
Practical Outcomes
- The study shows a promising experimental cancer therapy, but it offers no actionable guidance for longevity, metabolism, or performance. It remains a preclinical approach far from any DIY or clinical use for the biohacking community.
Summary
Scientists made tiny gold shells coated with a skin‑pigment hormone piece that sticks to melanoma cells. In mice, these particles gathered in the tumors and, when hit with a low‑energy infrared laser, they heated up and destroyed the cancer cells. This is a lab‑stage cancer treatment, not a health‑boosting tip for everyday use.
Abstract
To develop melanoma-targeted hollow gold nanospheres (HAuNS) and evaluate their potential utility for selective photothermal ablation in melanoma. A new class of photothermal coupling agents based on HAuNS was synthesized. HAuNS were stabilized with polyethylene glycol (PEG) coating and attached with alpha-melanocyte-stimulating hormone (MSH) analog, [Nle4,D-Phe7]alpha-MSH (NDP-MSH), which is a potent agonist of melanocortin type-1 receptor overexpressed in melanoma. The intracellular uptake of the NDP-MSH-conjugated PEGylated HAuNS (NDP-MSH-PEG-HAuNS) and the distribution of beta-arrestin were examined in murine B16/F10 melanoma cells. The biodistribution of NDP-MSH-PEG-HAuNS was assessed at 4 hours post i.v. injection in tumor-bearing nude mice. Photothermal ablation effect of the nanoparticles was evaluated both histologically using excised tissue and functionally by [18F]fluorodeoxyglucose positron emission tomography. NDP-MSH-PEG-HAuNS consist only of a thin gold wall with hollow interior (outer diameter, 43.5 +/- 2.3 nm; shell thickness, 3-4 nm), which displays strong and tunable resonance absorption in near-IR region (peak, 808 nm). The nanoparticles were specifically taken up by melanoma cells, which initiated the recruitment of beta-arrestins, the adapters to link the activated G-protein-coupled receptors to clathrin, indicating the involvement of receptor-mediated endocytosis. This resulted in enhanced extravasation of NDP-MSH-PEG-HAuNS from tumor blood vessels and their dispersion into tumor matrix compared with nonspecific PEGylated HAuNS. Successful selective photothermal ablation of B16/F10 melanoma with targeted HAuNS was confirmed by histologic and [18F]fluorodeoxyglucose positron emission tomography evaluation at 24 hours post near IR-region laser irradiation at a low-dose energy of 30 J/cm2. NDP-MSH-PEG-HAuNS have the potentials to mediate targeted photothermal ablation of melanoma.
Study Information
pubmed
2009
2009-02-01T00:00:00.000Z
10.1158/1078-0432.ccr-08-1480