Belotecan in ovarian cancer anti-inflammatory potential and mechanistic insight to nano-formulations
Abstract Background Ovarian cancer is a major gynecologic malignancy with high morbidity and mortality rates. Current treatment options have limited long-term effectiveness due to tumor resistance and significant side effects. Main body This article explores the potential of belotecan, a derivative of camptothecin, as a promising therapeutic agent for ovarian cancer. Belotecan’s ability to inhibit topoisomerase I, induce DNA damage, and modulate inflammation positions it as a strong candidate for enhancing ovarian cancer treatment. However, challenges such as poor bioavailability, rapid systemic clearance, and dose-limiting toxicity remain. To overcome these issues, nano-formulation strategies are proposed to improve pharmacokinetics, solubility, and tumor-specific targeting. These strategies may enhance belotecan's stability, increase its therapeutic efficacy, and minimize off-target effects. Conclusion This review provides a detailed examination of belotecan’s molecular mechanisms, its anti-inflammatory and anti-cancer properties, and the advances in nano-formulation technologies. The integration of these strategies could lead to more effective treatments and improved outcomes for ovarian cancer patients. Graphical abstract
Authors
- Shafiul Haque (ORCID: https://orcid.org/0000-0002-2989-121X)
- Dr Gesu Singla
- Bunty Sharma
- Sandeep Kaur
- Ajay Kumar
- Poonam Chaturvedi
- Amita
- Brahmjot Singh
- Pooja Sharma
Institutions
- Chandigarh University (IN)
- Maharishi Markandeshwar University, Mullana (IN)
- Guru Jambheshwar University of Science and Technology (IN)
- Guru Nanak Dev University (IN)
- Adesh University (IN)
- Universidad Espíritu Santo (EC)
- Graphic Era University (IN)
- Jazan University (SA)
Publication Details
- Journal
- Future Journal of Pharmaceutical Sciences
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1186/s43094-026-00940-9
- Primary Topic
- Cancer therapeutics and mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00