# In Vitro and In Silico Evaluation of the Potential Anti-Prostate Cancer Activity of Rosmarinus officinalis L. Leaf Extracts

**Authors:** Samantha Franchette B. Austria, Mon-Juan Lee, Kathlia A. De Castro-Cruz, Pang-Hung Hsu, Cheng-Yang Hsieh, Steven Kuan-Hua Huang, Po-Wei Tsai

PMC · DOI: 10.3390/ijms26104650 · International Journal of Molecular Sciences · 2025-05-13

## TL;DR

This study shows that rosemary leaf extracts have anti-prostate cancer effects, with water extracts being more effective than ethanol ones.

## Contribution

The study combines in vitro and in silico methods to evaluate rosemary's anti-cancer potential against prostate cancer.

## Key findings

- Water extract of rosemary showed higher cytotoxicity than ethanol extract in DU-145 cells.
- Carnosol and rosmarinic acid showed strong interactions with key prostate cancer targets like TP53.
- Rosmarinic acid was identified as a promising candidate due to its low toxicity and strong binding.

## Abstract

Prostate cancer is one of the most prevalent cancer types diagnosed in older men. Investigations into traditional medicines like Rosmarinus officinalis L., popularly known as rosemary, are a current research interest due to its anti-cancer properties. This study investigates the cytotoxicity of aqueous and ethanolic rosemary leaf extracts in DU-145 cells and the interaction of its active metabolites with key prostate cancer targets using an in silico approach. The water extract of rosemary leaves showed greater cytotoxicity than the ethanol extract, with IC50 values of 1.4140 ± 0.1138 mg/mL and 1.8666 ± 0.0367 mg/mL, respectively; the highest cytotoxic effects for both extracts were observed at 5 mg/mL. These findings indicate significant cytotoxic differences based on concentration and solvent. Network pharmacology identified 37 genes linked to prostate adenocarcinoma, highlighting key genes like EGFR, TP53, ERBB2, IGFBP3, MMP-2, MMP-9, HDAC6, PDGFRB, and FGFR1. Molecular dynamics simulations and binding energy calculations revealed strong interactions between carnosol and rosmarinic acid with these targets, with TP53–carnosol showing the most stable conformation. Rosmarinic acid was identified as a promising candidate due to its low toxicity. This study demonstrates the potential anti-prostate cancer properties of rosemary leaf extracts for further investigations on the development of drugs against prostate cancer.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956], TP53 (tumor protein p53) [NCBI Gene 7157], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064], IGFBP3 (insulin like growth factor binding protein 3) [NCBI Gene 3486], MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313], MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318], HDAC6 (histone deacetylase 6) [NCBI Gene 10013], PDGFRB (platelet derived growth factor receptor beta) [NCBI Gene 5159], FGFR1 (fibroblast growth factor receptor 1) [NCBI Gene 2260]
- **Chemicals:** carnosol (PubChem CID 442009), rosmarinic acid (PubChem CID 639655)
- **Diseases:** prostate cancer (MONDO:0005159), prostate adenocarcinoma (MONDO:0005082)

## Full-text entities

- **Diseases:** cytotoxic (MESH:D064420), cancer (MESH:D009369), prostate adenocarcinoma (MESH:D000230), Prostate Cancer (MESH:D011471)
- **Chemicals:** water (MESH:D014867), ethanol (MESH:D000431), Rosmarinic acid (MESH:C041376), carnosol (MESH:C068623)
- **Species:** Homo sapiens (human, species) [taxon 9606], Salvia rosmarinus (rosemary, species) [taxon 39367]
- **Cell lines:** DU-145 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0105)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12111643/full.md

## References

119 references — full list in the complete paper: https://tomesphere.com/paper/PMC12111643/full.md

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Source: https://tomesphere.com/paper/PMC12111643