# Gene expression analysis of epithelial-mesenchymal transition markers in oral submucous fibrosis fibroblasts treated with arecoline

**Authors:** Jigar P Thakkar, Gopal Srivastava, Khushali Shah, Vipin Arora, Mony Behera, Sameer Gupta

PMC · DOI: 10.6026/973206300213871 · 2025-10-31

## TL;DR

This study shows that curcumin and EGCG can reverse arecoline-induced changes in fibroblasts linked to oral submucous fibrosis.

## Contribution

The study demonstrates that curcumin is more effective than EGCG in inhibiting EMT caused by arecoline in OSF fibroblasts.

## Key findings

- Arecoline induces EMT by reducing E-cadherin and increasing N-cadherin, vimentin, α-SMA, Snail, and Twist.
- Curcumin and EGCG significantly reverse arecoline-induced EMT markers and migration in OSF fibroblasts.
- Curcumin shows greater efficacy than EGCG in inhibiting EMT in OSF fibroblasts.

## Abstract

Oral submucous fibrosis (OSF), a potentially malignant disorder, is strongly linked to areca nut consumption, with arecoline inducing
epithelial-mesenchymal transition (EMT) in fibroblasts. Therfeore, it is of interest to investigate EMT marker expression in OSF
fibroblasts exposed to arecoline and assessed the inhibitory effects of curcumin and epigallocatechin-3-gallate (EGCG). Primary
fibroblasts from OSF and normal mucosa were treated and EMT markers were analyzed by RT-qPCR, Western blotting and wound healing assays.
Arecoline decreased E-cadherin and increased N-cadherin, vimentin, α-SMA, Snail, Twist and migration rate, whereas co-treatment with
curcumin or EGCG significantly reversed these effects, with curcumin showing greater efficacy. Thus, we show that curcumin and EGCG
inhibit arecoline-induced EMT and may serve as potential therapeutic agents in OSF management.

## Linked entities

- **Genes:** shg (shotgun) [NCBI Gene 37386], CadN (Cadherin-N) [NCBI Gene 35070], PRELID1 (PRELI domain containing 1) [NCBI Gene 737446], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58], SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615], TWIST1 (twist family bHLH transcription factor 1) [NCBI Gene 7291]
- **Chemicals:** arecoline (PubChem CID 2230), curcumin (PubChem CID 969516), epigallocatechin-3-gallate (PubChem CID 65064), EGCG (PubChem CID 65064)
- **Diseases:** oral submucous fibrosis (MONDO:0018166)

## Full-text entities

- **Genes:** CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}, SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615] {aka SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1}, TWIST1 (twist family bHLH transcription factor 1) [NCBI Gene 7291] {aka ACS3, BPES2, BPES3, CRS, CRS1, CSO}, CDH2 (cadherin 2) [NCBI Gene 1000] {aka ACOGS, ADHD8, ARVD14, CD325, CDHN, CDw325}, VIM (vimentin) [NCBI Gene 7431]
- **Diseases:** OSF (MESH:D009914)
- **Chemicals:** Arecoline (MESH:D001115), curcumin (MESH:D003474), EGCG (MESH:C045651)

---
Source: https://tomesphere.com/paper/PMC12859285