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Potential Role of Thymoquinone to Treat Gastrointestinal Cancers: Insights Into Its Molecular Mechanisms Publisher



Rahjoo T1, 2 ; Motamedzadeh A3 ; Ferdosi F4 ; Dadgostar E5, 6 ; Aschner M7 ; Mirzaei H8 ; Ghesmatpour S1, 2 ; Nabavizadeh F1, 2 ; Rahmatidehkordi F9 ; Tamtaji OR1, 2
Authors
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Authors Affiliations
  1. 1. Electrophysiology Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Internal Medicine, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran
  4. 4. Department of Radiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Behavioral Sciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  6. 6. Student Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran
  7. 7. Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, 10461, NY, United States
  8. 8. Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran
  9. 9. Students’ Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Naunyn-Schmiedeberg's Archives of Pharmacology Published:2025


Abstract

Gastrointestinal (GI) malignancies, including esophageal cancer, gastric cancer, and colon cancer, are associated with high mortality rates worldwide. Thymoquinone is one of the main bioactive components of Nigella sativa, and it has been documented to have anticancer effects including GI cancer. Thymoquinone inhibits GI cancer progression by inducing cell cycle arrest, apoptosis, and oxidative stress and inhibiting inflammation, migration, invasion, metastasis, histone deacetylases, STAT3, PI3K/AKT/mTOR, and Wnt/β-catenin signaling pathways. Although the beneficial effects of thymoquinone have been documented, some limitations, including poor bioavailability and hydrophobicity, have hindered its clinical application. Nanotechnology approaches bypass these limitations. In this review article, we outline the different cellular and molecular pathways influenced by thymoquinone and its nanoformulations in GI cancer. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2025.
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