# Cannabinoid Signaling and Autophagy in Oral Disease: Molecular Mechanisms and Therapeutic Implications

**Authors:** Undral Munkhsaikhan, Md Ataur Rahman, Alivia Shasteen, Karima Ait-Aissa, Amal M. Sahyoun, Rajat Das Gupta, Modar Kassan, Ehsanul Hoque Apu, Ammaar H. Abidi

PMC · DOI: 10.3390/ijms27010525 · International Journal of Molecular Sciences · 2026-01-04

## TL;DR

This paper explores how cannabinoids affect autophagy in oral diseases, suggesting potential new therapies for conditions like oral cancer and gum disease.

## Contribution

The paper reviews novel molecular mechanisms linking cannabinoid signaling to autophagy regulation in oral tissues and highlights therapeutic opportunities.

## Key findings

- Cannabinoids modulate autophagy via mTOR, AMPK, and Beclin-1 pathways in oral tissues.
- Cannabinoid-induced autophagy may enhance stem cell survival and aid dental pulp regeneration.
- Challenges include receptor selectivity, bioavailability, and regulatory constraints for clinical use.

## Abstract

Autophagy is a well-preserved biological mechanism that is essential for sustaining homeostasis by degradation and recycling damaged organelles, misfolded proteins, and other cytoplasmic detritus. Cannabinoid signaling has emerged as a prospective regulator of diverse cellular functions, including immunological modulation, oxidative stress response, apoptosis, and autophagy. Dysregulation of autophagy contributes to pathogenesis and treatment resistance of several oral diseases, including oral squamous cell carcinoma (OSCC), periodontitis, and gingival inflammation. This review delineates the molecular crosstalk between cannabinoid receptor type I (CB1) and type II (CB2) activation and autophagic pathways across oral tissues. Cannabinoids, including cannabidiol (CBD) and tetrahydrocannabinol (THC), modulate key regulators like mTOR, AMPK, and Beclin-1, thereby influencing autophagic flux, inflammation, and apoptosis. Experimental studies indicate that cannabinoids inhibit the PI3K/AKT/mTOR pathway, promote reactive oxygen species (ROS)-induced autophagy, and modulate cytokine secretion, mechanisms that underline their dual anti-inflammatory and anti-cancer capabilities. In addition, cannabinoid-induced autophagy has been shown to enhance stem cell survival and differentiation, offering promise for dental pulp regeneration. Despite these promising prospects, several challenges remain, including receptor selectivity, dose-dependent variability, limited oral bioavailability, and ongoing regulatory constraints. A deeper understanding of the context-dependent regulation of autophagy by cannabinoid signaling could pave the way for innovative therapeutic interventions in dentistry. Tailored cannabinoid-based formulations, engineered for receptor specificity, tissue selectivity, and optimized delivery, hold significant potential to revolutionize oral healthcare by modulating autophagy-related molecular pathways involved in disease resolution and tissue regeneration.

## Linked entities

- **Proteins:** MTOR (mechanistic target of rapamycin kinase), PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1), BECN1 (beclin 1), PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1)
- **Chemicals:** cannabidiol (PubChem CID 644019), tetrahydrocannabinol (PubChem CID 16078)
- **Diseases:** oral squamous cell carcinoma (MONDO:0004958), periodontitis (MONDO:0005076)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, CNR2 (cannabinoid receptor 2) [NCBI Gene 1269] {aka CB-2, CB2, CX5}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562] {aka AMPK, AMPK alpha 1, AMPKa1}, CNR1 (cannabinoid receptor 1) [NCBI Gene 1268] {aka CANN6, CB-R, CB1, CB1A, CB1K5, CB1R}, BECN1 (beclin 1) [NCBI Gene 8678] {aka ATG6, VPS30, beclin1}
- **Diseases:** periodontitis (MESH:D010518), gingival inflammation (MESH:D007249), cancer (MESH:D009369), Oral Disease (MESH:D009059), OSCC (MESH:D000077195)
- **Chemicals:** CBD (MESH:D002185), ROS (MESH:D017382), THC (MESH:D013759), Cannabinoid (MESH:D002186)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786432/full.md

## References

101 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786432/full.md

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Source: https://tomesphere.com/paper/PMC12786432