# Cannabidiol as a Prophylactic Agent Against Glioblastoma Growth: A Preclinical Investigation

**Authors:** Lei P. Wang, Bidhan Bhandari, Sahar Emami Naeini, Breanna Hill, Hannah M. Rogers, Jules Gouron, Nayeli Perez-Morales, Aruba Khan, William Meeks, Ahmed El-Marakby, Nancy Young, Fernando L. Vale, Salman Ali, Gerald Wallace, Jack C. Yu, Ali S. Arbab, Évila Lopes Salles, Babak Baban

PMC · DOI: 10.3390/ijms27020757 · 2026-01-12

## TL;DR

CBD pretreatment may help prevent glioblastoma growth by altering the tumor environment and immune response.

## Contribution

This study is the first to show CBD pretreatment can reduce glioblastoma progression by modulating immune and molecular factors.

## Key findings

- CBD pretreatment for 14 days significantly reduced tumor burden in mice.
- CBD pretreatment decreased expressions of IDO, PD-L1, MGMT, and Ki67, indicating a less aggressive tumor phenotype.
- CBD exposure primed the tumor microenvironment toward an anti-tumor state.

## Abstract

Glioblastoma (GBM) remains one of the most lethal brain tumors, with current therapies offering limited benefits and high relapse rates. This study presents the first preclinical evidence that pretreatment with inhaled cannabidiol (CBD) before tumor establishment can markedly inhibit GBM progression. We hypothesized that early CBD exposure could prime the immune and molecular landscape to resist tumor growth. C57BL/6 mice were pretreated with inhaled CBD for 3 or 14 days, or with placebo, prior to intracranial implantation of glioblastoma cells. Tumor growth, immune checkpoint expressions (IDO, PD-L1), and key biomarkers (MGMT, Ki67) were analyzed to evaluate tumor dynamics and immune modulation. Fourteen-day CBD pretreatment significantly reduced tumor burden compared with both placebo and 3-day CBD groups, accompanied by decreased IDO, PD-L1, MGMT, and Ki67 expression, which are signatures of a less aggressive tumor phenotype. These findings suggest that prolonged CBD exposure can precondition the tumor microenvironment toward an anti-tumor state, improving disease control and potentially lowering relapse risk. This study introduces a novel concept of CBD pretreatment as an immune-modulatory strategy with high translational potential for glioblastoma management.

## Linked entities

- **Genes:** IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620], CD274 (CD274 molecule) [NCBI Gene 29126], MGMT (O-6-methylguanine-DNA methyltransferase) [NCBI Gene 4255], Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345]
- **Chemicals:** cannabidiol (PubChem CID 644019), CBD (PubChem CID 644019)
- **Diseases:** glioblastoma (MONDO:0018177), GBM (MONDO:0018177)

## Full-text entities

- **Genes:** Cd274 (CD274 antigen) [NCBI Gene 60533] {aka A530045L16Rik, B7h1, Pdcd1l1, Pdcd1lg1, Pdl1}, Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345] {aka D630048A14Rik, Ki-67, Ki67}, Ido1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 15930] {aka Ido, Indo}, Mgmt (O-6-methylguanine-DNA methyltransferase) [NCBI Gene 17314] {aka AGT, Agat}
- **Diseases:** brain tumors (MESH:D001932), GBM (MESH:D005909), Tumor (MESH:D009369)
- **Chemicals:** CBD (MESH:D002185)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12841290/full.md

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Source: https://tomesphere.com/paper/PMC12841290