4.6 Review

Antitumoral Effects of Tricyclic Antidepressants: Beyond Neuropathic Pain Treatment

Journal

CANCERS
Volume 14, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/cancers14133248

Keywords

tricyclic antidepressants; antitumor therapy; imipramine; central nervous system; drug repurposing

Categories

Funding

  1. Instituto de Salud Carlos III (Spanish Ministry of Health)
  2. FEDER funds [PI15/00626, PI18/00144, ICI20/00044]
  3. Spanish Society of Hematology and Hemotherapy (FEHH/Janssen)
  4. Ministry of Universities, Government of Spain

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This review discusses the application of tricyclic antidepressants (TCAs) in the field of cancer treatment. The current evidence shows that TCAs can safely and effectively treat neuropathic pain and have anti-tumor effects by blocking crucial molecular pathways in cancer cells. Ongoing clinical trials provide new directions for the use of TCAs as antineoplastic drugs.
Simple Summary Tricyclic antidepressants (TCAs) are old and known therapeutic agents whose good safety profile makes them good candidates for drug repurposing. As the relevance of nerves in cancer development and progression is being unveiled, attention now turns to the use of nerve-targeting drugs, such as TCAs, as an interesting approach to combat cancer. In this review, we discuss current evidence about the safety of TCAs, their application to treat neuropathic pain in cancer patients, and in vitro and in vivo demonstrations of the antitumoral effects of TCAs. Finally, the results of ongoing clinical trials and future directions are discussed. Growing evidence shows that nerves play an active role in cancer development and progression by altering crucial molecular pathways and cell functions. Conversely, the use of neurotropic drugs, such as tricyclic antidepressants (TCAs), may modulate these molecular signals with a therapeutic purpose based on a direct antitumoral effect and beyond the TCA use to treat neuropathic pain in oncology patients. In this review, we discuss the TCAs' safety and their central effects against neuropathic pain in cancer, and the antitumoral effects of TCAs in in vitro and preclinical studies, as well as in the clinical setting. The current evidence points out that TCAs are safe and beneficial to treat neuropathic pain associated with cancer and chemotherapy, and they block different molecular pathways used by cancer cells from different locations for tumor growth and promotion. Likewise, ongoing clinical trials evaluating the antineoplastic effects of TCAs are discussed. TCAs are very biologically active compounds, and their repurposing as antitumoral drugs is a promising and straightforward approach to treat specific cancer subtypes and to further define their molecular targets, as well as an interesting starting point to design analogues with increased antitumoral activity.

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