# In Vitro Anti-Aging Effects of Yeast/Rice Fermentation Filtrate Combined with Sialic Acid in Cosmetic Applications

**Authors:** Fan Yang, Mingxuan Li, Yao Zuo, Lei Zhang, Jinyong Wu, Zhi Liu, Hua Wang

PMC · DOI: 10.3390/antiox14101184 · Antioxidants · 2025-09-28

## TL;DR

This study shows that combining yeast/rice fermentation filtrate with sialic acid boosts collagen production and reduces inflammation, offering a new approach for anti-aging cosmetics.

## Contribution

The study introduces a novel strategy to enhance collagen by simultaneously upregulating gene expression and stabilizing mRNA using RFF and SA.

## Key findings

- RFF and SA together significantly increased collagen gene transcription and mRNA stability.
- The combination reduced inflammatory markers like IL-1β, IL-6, and PGE2.
- RNA-seq showed modulation of genes in the IL-17 signaling pathway.

## Abstract

Oxidative stress and chronic inflammation are major contributors to skin aging, promoting collagen degradation and impairing dermal structure. These factors stimulate the expression of matrix metalloproteinases, accelerating collagen breakdown and leading to wrinkles, sagging, and loss of elasticity. Given the key role of collagen in maintaining skin firmness and integrity, strategies that enhance collagen synthesis are essential for anti-aging interventions. This study investigated the combined effects of Yeast/Rice Fermentation Filtrate (RFF) and sialic acid (SA) on collagen production, antioxidation, and anti-inflammation, as well as their underlying mechanisms. The combination of RFF and SA significantly increased collagen genes transcription and mRNA stability, thereby enhancing collagen accumulation in the extracellular matrix. RNA-seq analysis revealed that RFF and SA modulate genes involved in the IL-17 signaling pathway. Mechanistically, RFF enhanced collagen mRNA stability by regulating HuR, while SA promoted collagen gene transcription via the TGF-β/Smad pathway. Moreover, the combination reduced the expression of inflammatory markers (IL-1β, IL-6, IL-8, PGE2, and NO) and improved cellular resistance to oxidative and inflammatory stress. These findings support the application of RFF and SA in anti-aging cosmetics and propose a novel strategy to enhance collagen production by simultaneously upregulating gene expression and stabilizing collagen mRNA.

## Linked entities

- **Genes:** ELAVL1 (ELAV like RNA binding protein 1) [NCBI Gene 1994], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], Smox (Smad on X) [NCBI Gene 31738], IL1B (interleukin 1 beta) [NCBI Gene 3553], IL6 (interleukin 6) [NCBI Gene 3569], CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576], ptges2.L (prostaglandin E synthase 2 L homeolog) [NCBI Gene 100037123]
- **Chemicals:** sialic acid (PubChem CID 445063), RFF (PubChem CID 169408340), NO (PubChem CID 24822)

## Full-text entities

- **Diseases:** chronic inflammation (MESH:D007249)
- **Chemicals:** NO (MESH:D009614), SA (MESH:D019158)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12561143/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12561143/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12561143/full.md

---
Source: https://tomesphere.com/paper/PMC12561143