# Salacca zalacca extract's antiaging effect on aging genes, protein levels, and apoptosis in UV-induced fibroblast cells

**Authors:** Wahyu Widowati, Dani Dani, Vera Vera, Teresa L. Wargasetia, Fanny Rahardja, Fen Tih, Philips Onggowidjaja, Rita Tjokropranoto, Fadhilah H. Zahiroh, Rizal Azis, Didik Priyandoko, Wahyu Surakusumah, Dhanar S. Hadiprasetyo

PMC · DOI: 10.1016/j.jtumed.2025.05.005 · Journal of Taibah University Medical Sciences · 2025-06-09

## TL;DR

Snake fruit extract may help reduce skin aging caused by UV exposure by affecting genes and proteins linked to aging and cell death.

## Contribution

This study demonstrates the antiaging potential of Salacca zalacca extract in UV-induced fibroblast cells through gene and protein modulation.

## Key findings

- SZE increased COL1A1, FGF-2, and GPX-1 gene expression while decreasing MMP-1.
- SZE reduced levels of HAse, COX-2, and 8-OHdG proteins in UV-induced cells.
- SZE treatment reduced apoptosis and improved cell viability in fibroblasts.

## Abstract

Ultraviolet (UV) exposure can hasten the aging process of the skin. The use of chemicals for anti-aging has long-term adverse effects. The natural ingredients of snake fruit (Salacca zalacca L.) are known to have bioactive properties such as polyphenols, flavonoids, chlorogenic acid, and caffeic acid which have antiaging potential. The study aims to ascertain the potential of S. zalacca Extract (SZE) as an antiaging agent by in vitro assay.

The SZE compound content was analyzed by LC-MS/MS. SZE viability test on human skin fibroblast (BJ) cells was carried out using the WST assay. BJ cells were UV-induced as a cell model of premature aging. SZE 6.25, 12.5, and 25 μg/mL were administered to UV-induced BJ cells. The gene expression of COL1A1, MMP-1, FGF-2, and GPX-1 were analyzed by quantitative Real-Time PCR. Elastin (ELN), Hyaluronidase (HAse), Cyclooxigenase-2 (COX-2), 8-Hydroxydeoxyguanosine (8-OHdG), and Melatonin (MT) protein levels were analyzed by ELISA assay. The apoptosis of BJ cells was analyzed using flow cytometry. One-way ANOVA in SPSS Software was used for statistical analysis.

Treatment with SZE increased COL1A1, FGF-2, and GPX-1 gene expression and also decreased MMP-1 gene expression. SZE also increased ELN and MT levels in UV-induced BJ cells. After SZE treatment, the protein levels of HAse, COX-2, and 8-OHdG decreased compared to the positive control. SZE also succeeded in maintaining the lives of BJ cells and reducing apoptosis in BJ cells.

SZE has the potential to be an antiaging agent by in vitro assay.

## Linked entities

- **Genes:** COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277], MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312], FGF2 (fibroblast growth factor 2) [NCBI Gene 2247], GPX1 (glutathione peroxidase 1) [NCBI Gene 2876]
- **Proteins:** ELN (elastin), hasE (metalloprotease secretion protein), COX2 (cytochrome c oxidase subunit II), MCAT (malonyl-CoA-acyl carrier protein transacylase)
- **Chemicals:** chlorogenic acid (PubChem CID 1794427), caffeic acid (PubChem CID 689043)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277] {aka CAFYD, EDSARTH1, EDSC, OI1, OI2, OI3}, MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312] {aka CLG}, GPX1 (glutathione peroxidase 1) [NCBI Gene 2876] {aka GPXD, GSHPX1}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}
- **Chemicals:** flavonoids (MESH:D005419), polyphenols (MESH:D059808), S. zalacca Extract (-), 8-Hydroxydeoxyguanosine (MESH:D000080242), chlorogenic acid (MESH:D002726), MT (MESH:D008550), caffeic acid (MESH:C040048)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** BJ — Homo sapiens (Human), Telomerase immortalized cell line (CVCL_6573)

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12180987/full.md

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Source: https://tomesphere.com/paper/PMC12180987