# Exploring the Anticancer Potential of the Multistrain Probiotic Formulation OxxySlab in Bladder Cancer Cell Lines

**Authors:** Valeria Ciummo, Alessia Ciafarone, Serena Altamura, Francesca Lombardi, Marcella Reale, Maria Grazia Cifone, Benedetta Cinque, Paola Palumbo

PMC · DOI: 10.3390/antiox14111282 · 2025-10-26

## TL;DR

A new probiotic called OxxySlab may help treat bladder cancer by stopping cancer cell growth and migration while protecting healthy cells.

## Contribution

OxxySlab shows selective anticancer effects in bladder cancer cells through redox-mediated senescence and EMT inhibition.

## Key findings

- OxxySlab inhibited bladder cancer cell proliferation, clonogenicity, and migration.
- The treatment suppressed EMT and induced senescence in cancer cells.
- Normal urothelial cells remained unaffected, showing treatment selectivity.

## Abstract

Bladder cancer (BC), particularly its muscle-invasive subtype (MIBC), remains a clinical challenge due to high recurrence and limited therapeutic options. Emerging evidence suggests that probiotics may offer selective anticancer effects while preserving healthy tissue. In this study, we evaluated the antitumor potential of OxxySlab, a multistrain probiotic formulation, in two BC cell lines (T24 and 5637) and a non-tumorigenic urothelial cell line (SV-HUC1). OxxySlab lysate dose-dependently inhibited BC cell proliferation, clonogenicity, and migration, while sparing normal cells. Mechanistically, the treatment suppressed epithelial–mesenchymal transition (EMT), induced senescence, and disrupted redox homeostasis in malignant cells. These effects were associated with the induction of oxidative stress and impaired antioxidant defenses. Co-treatment with vitamin C attenuated ROS accumulation and senescence, implicating oxidative stress as a key mediator. Notably, SV-HUC1 cells retained viability and phenotype, confirming the formulation’s selectivity. Overall, these findings support OxxySlab as a promising adjunctive strategy in BC therapy, capable of reducing tumor aggressiveness through redox-mediated senescence and EMT inhibition without harming normal urothelial cells.

## Linked entities

- **Chemicals:** vitamin C (PubChem CID 54670067)
- **Diseases:** bladder cancer (MONDO:0004986)

## Full-text entities

- **Diseases:** tumor (MESH:D009369), BC (MESH:D001749)
- **Chemicals:** vitamin C (MESH:D001205), OxxySlab (-)
- **Cell lines:** SV-HUC1 — Homo sapiens (Human), Transformed cell line (CVCL_3798), 5637 — Homo sapiens (Human), Bladder carcinoma, Cancer cell line (CVCL_0126), T24 — Homo sapiens (Human), Bladder carcinoma, Cancer cell line (CVCL_0554)

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12649232/full.md

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Source: https://tomesphere.com/paper/PMC12649232