# Photobiomodulation Modulates the Response of Zoledronic-Acid-Treated Osteoblast-like SaOs-2 Cells: Implications for Bisphosphonate-Related Osteonecrosis

**Authors:** Rodrigo Antonio Carvalho Andraus, Ana Flávia Spadaccini Silva de Oliveira, Mário Celso Teixeira Lopes, Diego César Marques, Vanessa Gabriela Gonzales Marques, Deise Aparecida de Almeida Pires de Oliveira, Rodrigo Franco de Oliveira, Orlando Aguirres Guedes, Helder Fernandes de Oliveira, João Pedro Ribeiro Afonso, Iransé Oliveira Silva, Luiz Vicente Franco de Oliveira, Claudia Santos Oliveira, Regina Célia Poli, Luciana Prado Maia

PMC · DOI: 10.3390/bioengineering13010088 · Bioengineering · 2026-01-12

## TL;DR

This study shows that laser therapy can reduce the harmful effects of a drug used to treat bone diseases in lab cells, suggesting potential for preventing a rare but serious side effect.

## Contribution

The study demonstrates that photobiomodulation can modulate zoledronic acid-induced effects in osteoblast-like cells in a wavelength- and dose-dependent manner.

## Key findings

- PBM at 808 nm with 1 J increased metabolic activity in ZA-treated SaOs-2 cells.
- BCL-2 gene expression was upregulated by PBM at specific wavelengths and doses.
- PBM did not reverse apoptosis caused by zoledronic acid.

## Abstract

This study aimed to evaluate the effects of laser photobiomodulation (PBM) therapy in SaOs-2 osteosarcoma cells treated with zoledronic acid (ZA), a bisphosphonate, in vitro, mimicking a bisphosphonate-related osteonecrosis of the jaw (BRONJ) situation. Cells were treated with 100 μM ZA for 24 h and subjected to PBM using wavelengths of 660 nm and 808 nm at energy delivered of 1, 5, 10, and 20 J. After 24 h, metabolic activity, apoptosis, and BAX and BCL-2 gene expression were analyzed. Data were compared using one-way ANOVA followed by Tukey’s post hoc test (p < 0.05). ZA significantly reduced metabolic activity (p < 0.05), an effect attenuated by PBM at 808 nm with 1 J, while BCL-2 expression increased with 1 J at 660 nm and with 1 J and 20 J at 808 nm. However, PBM did not reverse ZA-induced apoptosis. In conclusion, PBM modulated the response of SaOs-2 osteoblastic cells treated with ZA in a wavelength- and dose-dependent manner. PBM at 808 nm and 1 J stimulated cell metabolic activity and upregulated BCL-2 expression, suggesting a potential protective effect against ZA-induced cytotoxicity.

## Linked entities

- **Genes:** BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596]
- **Chemicals:** zoledronic acid (PubChem CID 68740)

## Full-text entities

- **Genes:** BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}
- **Diseases:** osteosarcoma (MESH:D012516), Osteonecrosis (MESH:D010020), cytotoxicity (MESH:D064420), osteonecrosis of the jaw (MESH:D059266)
- **Chemicals:** ZA (MESH:D000077211), Bisphosphonate (MESH:D004164)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12838379/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12838379/full.md

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Source: https://tomesphere.com/paper/PMC12838379