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An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
Combined Effects of Gold Nanoparticles and Ionizing Radiation on Human Prostate and Lung Cancer Cell Migration
Elham Shahhoseini1, Bryce N Feltis2, Masao Nakayama3
1Discipline of Medical Radiation, School of Health and Biomedical Sciences, RMIT University, Bundoora 3083, Victoria, Australia. elham.shahhoseini@rmit.edu.au.
Abstract:
The effect of 15 nm-sized gold nanoparticles (AuNPs) and/or ionizing radiation (IR) on the migration and adhesion of human prostate (DU145) and lung (A549) cancer cell lines was investigated. Cell migration was measured by observing the closing of a gap created by a pipette tip on cell monolayers grown in 6-well plates. The ratio of the gap areas at 0 h and 24 h were used to calculate the relative migration. The relative migration of cells irradiated with 5 Gy was found to be 89% and 86% for DU145 and A549 cells respectively. When the cells were treated with 1 mM AuNPs this fell to ~75% for both cell lines. However, when the cells were treated with both AuNPs and IR an additive effect was seen, as the relative migration rate fell to ~60%. Of interest was that when the cells were exposed to either 2 or 5 Gy IR, their ability to adhere to the surface of a polystyrene culture plate was significantly enhanced, unlike that seen for AuNPs. The delays in gap filling (cell migration) in cells treated with IR and/or AuNPs can be attributed to cellular changes which also may have altered cell motility. In addition, changes in the cytoskeleton of the cancer cells may have also affected adhesiveness and thus the cancer cell's motility response to IR.
Insights
Gold nanoparticles (AuNPs) and ionizing radiation (IR) significantly reduced cancer cell migration. Combining AuNPs with IR had an additive effect, decreasing migration further and enhancing cell adhesion, suggesting potential therapeutic strategies.
Area of Science:
- Nanomedicine
- Radiation Oncology
- Cancer Biology
Background:
- Gold nanoparticles (AuNPs) are explored for cancer therapy.
- Ionizing radiation (IR) is a standard cancer treatment.
- Understanding combined effects on cancer cell behavior is crucial.
Purpose of the Study:
- To investigate the impact of 15 nm AuNPs and/or IR on human prostate (DU145) and lung (A549) cancer cell migration and adhesion.
- To determine if AuNPs and IR have additive or synergistic effects on cancer cell motility.
Main Methods:
- Cell migration assay: measuring gap closure in cell monolayers over 24 hours.
- Cell adhesion assay: assessing adherence to polystyrene culture plates.
- Treatment groups: control, AuNPs only, IR only (2 or 5 Gy), and combined AuNPs + IR.
Main Results:
- IR (5 Gy) reduced relative migration to 86-89%.
- 1 mM AuNPs reduced relative migration to ~75%.
- Combined AuNPs + IR reduced relative migration to ~60%, showing an additive effect.
- IR significantly enhanced cell adhesion, while AuNPs did not.
Conclusions:
- Combined AuNPs and IR exhibit an additive inhibitory effect on cancer cell migration.
- IR enhances cancer cell adhesion, a finding not observed with AuNPs.
- Observed changes in migration and adhesion may be linked to alterations in cell motility and cytoskeleton.
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