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Surface-enhanced Resonance Raman Scattering Nanoprobe Ratiometry for Detecting Microscopic Ovarian Cancer via Folate Receptor Targeting
Published on: March 25, 2019
Analysis of the molecular alterations in cancer cells following nanotechnology-assisted targeted radiotherapy using
Naser Jafarzadeh1, Rasoul Malekfar2, Marzieh Nadafan3
1Department of Medical Physics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Abstract:
The study unveiled an innovative strategy for precise radiation targeting in cancer treatment, along with the monitoring of molecular changes induced by this therapeutic approach. In this research, we explored the impact of administering anti-HER2-AgNPs nanoconjugates either individually or in conjunction with gamma irradiation on the viability of SKBR3 breast cancer cells. The utilization of nanoconjugates resulted in an enhancement of cellular sensitivity toward radiation. The viability of the cells exhibited a decline as the dose of irradiation increased, and this decrease was further exacerbated by the passage of time following irradiation. The analysis of RS revealed distinct cellular responses in varying conditions. The observed increase in SERS intensity, resulting from the increment in dose from 0 to 2 Gy, can be attributed to the probable upregulation of HER2 expression induced by irradiation. The observed decrease in SERS intensity at doses of 4 and 6 Gy can be attributed to the likely reduction in HER2 expression. It was illustrated that the analysis of Raman spectroscopy data can aid in the identification of radiation-induced biochemical alterations in cancer cells during the application of nanoconjugates-based radiotherapy. The findings revealed that nanoconjugates have the potential to enhance cellular sensitivity to radiation along with facilitating the detection of radiation-induced biochemical alterations within cancer cells.
Insights
This study shows that anti-HER2-AgNPs nanoconjugates improve cancer cells' sensitivity to radiation therapy. Raman spectroscopy detected radiation-induced molecular changes, aiding treatment monitoring.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Cancer radiotherapy faces challenges in precise targeting and monitoring molecular responses.
- HER2-positive breast cancers are a significant clinical concern.
- Nanoparticle-drug conjugates offer potential for targeted cancer therapy.
Purpose of the Study:
- To investigate the combined effect of anti-HER2-AgNPs nanoconjugates and gamma irradiation on SKBR3 breast cancer cell viability.
- To monitor radiation-induced molecular alterations using Raman spectroscopy (RS) in conjunction with nanoconjugates.
Main Methods:
- SKBR3 breast cancer cells were treated with anti-HER2-AgNPs nanoconjugates alone or combined with varying doses of gamma irradiation.
- Cell viability was assessed after irradiation.
- Surface-enhanced Raman spectroscopy (SERS) was employed to analyze molecular changes.
Main Results:
- Nanoconjugates enhanced cellular sensitivity to radiation therapy.
- Increased irradiation dose led to decreased cell viability, with effects amplified over time.
- RS analysis indicated dose-dependent changes in HER2 expression, with potential upregulation at 2 Gy and downregulation at 4-6 Gy.
- SERS intensity correlated with irradiation dose, reflecting biochemical alterations.
Conclusions:
- Anti-HER2-AgNPs nanoconjugates can potentiate radiation therapy efficacy in HER2-positive breast cancer cells.
- Raman spectroscopy analysis of nanoconjugate-treated cells can identify radiation-induced biochemical changes.
- This approach holds promise for monitoring and optimizing nanoconjugate-based radiotherapy.
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