Isotretinoin as a Multifunctional Anticancer Agent: Molecular Mechanisms, Pharmacological Insights and Therapeutic
Pritam Sarkar1, Nasrin Sultana1, Prottoy Kumar Debnath1
1Pharmacy Discipline, Khulna University, Khulna, Bangladesh.
Abstract:
Despite notable advancements in conventional cancer therapies, challenges such as drug resistance, adverse effects, and high treatment costs remain significant obstacles. This situation calls for exploring new therapeutic options. One promising approach is drug repurposing, which uses existing medications with known effects to identify new anticancer agents. Isotretinoin (13-cis-retinoic acid), a vitamin A derivative typically used to treat severe acne, shows considerable potential as an anticancer agent. Recent studies suggest that isotretinoin has the potential to enhance the efficacy of cancer treatment and contribute to cancer inhibition by targeting specific molecular pathways. This review explores isotretinoin's chemistry, pharmacokinetics, and toxicity, emphasizing its role in cancer treatment through clinical and preclinical studies while elucidating its anticancer mechanisms. Both preclinical and clinical studies have revealed that isotretinoin can effectively inhibit the growth of tumor cells, induce apoptosis, and help regulate cellular differentiation in a range of cancers, including neuroblastoma, glioblastoma, breast, skin, lung, ovarian, cervical, and head and neck cancers. Isotretinoin works against cancer through several mechanisms. It activates retinoic acid receptors (RARs), suppresses oncogenic signaling pathways, and influences gene transcription related to cell cycle control and apoptosis. Moreover, combining isotretinoin with other treatments, like interferon-alpha, chemotherapy drugs, or other targeted inhibitors, can create synergistic effects that improve treatment effectiveness and potentially lessen side effects. Although isotretinoin holds great promise, we still need more research to address its limitations, such as its toxicity, risks during pregnancy, and differing responses in various cancer types. Current research focuses on optimizing isotretinoin-based therapies by refining dosage regimens to maximize efficacy and enhancing formulation strategies for improved absorption and reduced side effects. Ultimately, the use of isotretinoin in cancer treatment demonstrates the potential of repurposing established drugs and paves the way for more accessible and cost-effective cancer therapies.
Insights
Isotretinoin, a repurposed acne drug, shows promise in cancer treatment by inhibiting tumor growth and inducing apoptosis. Further research is needed to optimize its use and address toxicity for more accessible therapies.
Area of Science:
- Oncology
- Pharmacology
- Drug Repurposing
Background:
- Conventional cancer therapies face challenges like drug resistance, adverse effects, and high costs.
- Drug repurposing offers a promising avenue for identifying novel anticancer agents from existing medications.
Purpose of the Study:
- To review the chemistry, pharmacokinetics, toxicity, and anticancer mechanisms of isotretinoin.
- To explore the clinical and preclinical evidence supporting isotretinoin's role in cancer treatment.
Main Methods:
- Literature review of preclinical and clinical studies on isotretinoin in cancer.
- Analysis of isotretinoin's molecular mechanisms, including receptor activation and pathway modulation.
Main Results:
- Isotretinoin effectively inhibits tumor cell growth, induces apoptosis, and regulates differentiation across various cancers.
- Mechanisms include retinoic acid receptor (RAR) activation and suppression of oncogenic pathways.
- Combination therapies with isotretinoin show synergistic effects, potentially improving efficacy and reducing side effects.
Conclusions:
- Isotretinoin demonstrates significant potential as an anticancer agent through multiple mechanisms.
- Further research is required to optimize dosage, formulation, and address toxicity for broader clinical application.
- Drug repurposing of isotretinoin offers a pathway to more cost-effective cancer therapies.
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