EN
Investigation of Endoplasmic Reticulum Stress and Apoptosis Caused by Malachite Green-Mediated Sonodynamic Therapy in HL60 Cells
Abstract
Aim: Sonodynamic antitumor therapy is a promising, novel method for the treatment of cancer. To determine the effects of malachite green (MG) in the presence of ultrasound (US), MG was tested in vitro on HL60 cells at different concentrations as a sonodynamic compound. We investigated cell viability, morphology, and the occurrence of ER stress after MG-mediated sonodynamic therapy (SDT) in HL60 cells.
Aim: Sonodynamic antitumor therapy is a promising, novel method for the treatment of cancer. To determine the effects of malachite green (MG) in the presence of ultrasound (US), MG was tested in vitro on HL60 cells at different concentrations as a sonodynamic compound. We investigated cell viability, morphology, and the occurrence of endoplasmic reticulum (ER) stress after MG-mediated sonodynamic therapy (SDT) in HL60 cells.
Material and Method: Four groups were formed, including a control group, a group subjected to ultrasound (US) only, a group treated with various concentrations of MG, and a group treated with US using the same concentrations. The cells were treated with 1MHz ultrasound at 2 W/cm2 for 3 minutes. The assessment of cell viability was conducted 24 hours post-treatment through the utilization of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay. Cell morphology and apoptotic index were determined using Giemsa staining, while GRP78 and PERK expressions were determined through immunocytochemistry staining.
Results: The cell cytotoxicity of HL60 cells significantly increased after MG-mediated sonodynamic therapy. After treatment, apoptotic cells with micronuclei were observed morphologically. Significant levels of GRP78 and PERK expression were observed in all groups, except for PERK expression in the US group, compared to the control group.
Conclusion: The induction of ER stress, accompanied by intense apoptosis and a marked decrease in cell viability, demonstrates the potential of MG-mediated sonodynamic therapy in cancer treatment. Investigating ER stress as a molecular target may contribute to improving the treatment method.
Keywords
Destekleyen Kurum
The authors declared that this study has received no financial support.
Etik Beyan
Since the methodological structure of the study is a "cell culture study", it does not require ethics committee approval in accordance with the World Medical Association Declaration of Helsinki "Ethical Principles for Medical Research on Humans"
Kaynakça
- Miller KD, Nogueira L, Devasia T, et al. Cancer treatment and survivorship statistics. Cancer J Clin. 2022;72:409-36.
- Zou L, Wang H, He B, et al. Current approaches of photothermal therapy in treating cancer metastasis with nanotherapeutics.Theranostics. 2016;6:762-72.
- Correia JH, Rodrigues JA, Pimenta S, et al Photodynamic therapy review: principles, photosensitizers, applications, and future directions. Pharmaceutics. 2021;13:1332.
- Qian X, Zheng Y, Chen Y. Micro/nanoparticle-augmented sonodynamic therapy (SDT): breaking the depth shallow of photoactivation. Adv Mater. 2016;28:8097-129.
- Yumita N, Nishigaki R, Umemura K, Umemura S. Hematoporphyrin as a sensitizer of cell-damaging effect of ultrasound. Jpn J Cancer Res.1989;80:219-22.
- Gong F, Cheng L, Yang N, et al. Ultrasmall oxygen-deficient bimetallic oxide MnWOX nanoparticles for depletion of endogenous GSH and enhanced sonodynamic cancer therapy. Adv Mater. 2019;31:1900730.
- Son S, Kim JH, Wang X, et al. Multifunctional sonosensitizers in sonodynamic cancer therapy. Chem Soc Rev. 2020;49:3244-61.
- Chen H, Zhou X, Gao Y, et al. Recent progress in development of new sonosensitizers for sonodynamic cancer therapy. Drug DiscovToday. 2014;19:502-9.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Tıp Fiziği , Tıbbi ve Biyolojik Fizik (Diğer)
Bölüm
Araştırma Makalesi
Yayımlanma Tarihi
31 Ocak 2024
Gönderilme Tarihi
27 Kasım 2023
Kabul Tarihi
23 Aralık 2023
Yayımlandığı Sayı
Yıl 2024 Cilt: 6 Sayı: 1