Analysis of the molecular alterations in cancer cells following nanotechnology-assisted targeted radiotherapy using Raman spectroscopy.

Cancer Molecular changes Radiotherapy Raman spectroscopy Targeted-therapy

Journal

Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine
ISSN: 1872-9800
Titre abrégé: Appl Radiat Isot
Pays: England
ID NLM: 9306253

Informations de publication

Date de publication:
01 Feb 2024
Historique:
received: 01 10 2023
revised: 27 01 2024
accepted: 31 01 2024
medline: 7 2 2024
pubmed: 7 2 2024
entrez: 6 2 2024
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 38320379
pii: S0969-8043(24)00051-4
doi: 10.1016/j.apradiso.2024.111223
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111223

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Fereshteh Koosha reports financial support was provided by Shahid Beheshti University of Medical Sciences.

Auteurs

Naser Jafarzadeh (N)

Department of Medical Physics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. Electronic address: naser.jafarzadeh@modares.ac.ir.

Rasoul Malekfar (R)

Atomic & Molecular Group, Department of Physics, Tarbiat Modares University, Tehran, Iran.

Marzieh Nadafan (M)

Department of Physics, Shahid Rajaee Teacher Training University, Tehran, P. O. Box 16788-15811, Iran.

Samira Eynali (S)

Radiation Biology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.

Fereshteh Koosha (F)

Department of Radiology Technology, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: f.koosha@sbmu.ac.ir.

Mohammad Satari (M)

Department of Biology, Faculty of Science, Malayer University, Malayer, Iran.

Classifications MeSH