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D-Allose: Molecular Pathways and Therapeutic Capacity in Cancer Publisher Pubmed



Khajeh S1 ; Ganjavi M2 ; Panahi G3 ; Zare M4 ; Zare M4 ; Tahami SM1 ; Razban V6, 7
Authors
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Authors Affiliations
  1. 1. Bone and Joint Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  2. 2. Nutritional Sciences Pro-gram, School of Community Health & Policy, Morgan State University, MD, United States
  3. 3. Department of Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  5. 5. School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  6. 6. Department of Molecular Medicine, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
  7. 7. Stem Cell Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

Source: Current Molecular Pharmacology Published:2023


Abstract

Background: Despite the implementation of various cancer therapies, adequate therapeutic efficacy has not been achieved. A growing number of studies have been dedicated to the discovery of new molecules to combat refractory cancer cells efficiently. Recently, the use of a rare type of sugar, D-allose, has attracted the attention of research communities. In combination with the first-line treatment of cancers, including different types of radiotherapies and chemotherapies, D-allose has been detected with favorable complementary effects. Understanding the mechanism of therapeutic target molecules will enable us to develop new strategies for cancer patients that do not currently respond to the present therapies. Objective: We aimed to provide a review of the effects of D-allose in cancer treatment, its mechanisms of action, and gaps in this field that require more investigations. Discussion: With rare exceptions, in many cancer types, including head and neck, lung, liver, bladder, blood, and breast, D-allose consistently has exhibited anticancer activity in vitro and/or in vivo. Most of the D-allose functions are mediated through thioredoxin-interacting protein molecules. D-allose exerts its effects via reactive oxygen species regulation, cell cycle arrest, metabolic reprogramming, au-tophagy, apoptosis induction, and sensitizing tumors to radiotherapy and chemotherapy. Conclusion: D-allose has shown great promise for combating tumor cells with no side effects, especially in combination with first-line drugs; however, its potential for cancer therapy has not been com-prehensively investigated in vitro or in vivo. © 2023 Bentham Science Publishers.