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The role and its mechanism of intermittent fasting in tumors: friend or foe?
- Source :
- Cancer Biology & Medicine, Cancer Biology & Medicine, Vol 18, Iss 1, Pp 63-73 (2021)
- Publication Year :
- 2021
- Publisher :
- Compuscript, 2021.
-
Abstract
- Intermittent fasting (IF) is becoming a prevailing topic worldwide, as it can cause changes in the body's energy metabolism processes, improve health, and affect the progression of many diseases, particularly in the circumstance of oncology. Recent research has shown that IF can alter the energy metabolism of tumor cells, thereby inhibiting tumor growth and improving antitumor immune responses. Furthermore, IF can increase cancer sensitivity to chemotherapy and radiotherapy and reduce the side effects of these traditional anticancer treatments. IF is therefore emerging as a promising approach to clinical cancer treatment. However, the balance between long-term benefits of IF compared with the harm from insufficient caloric intake is not well understood. In this article, we review the role of IF in tumorigenesis and tumor therapy, and discuss some scientific problems that remain to be clarified, which might provide some assistance in the application of IF in clinical tumor therapy.
- Subjects :
- 0301 basic medicine
Cancer Research
tumor
Diet, Reducing
Carcinogenesis
medicine.medical_treatment
Intermittent fasting
Review
Bioinformatics
medicine.disease_cause
lcsh:RC254-282
03 medical and health sciences
0302 clinical medicine
Immune system
Neoplasms
energy metabolism
medicine
Animals
Humans
Chemotherapy
Mechanism (biology)
business.industry
immune escape
Cancer
Immunotherapy
Fasting
medicine.disease
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Radiation therapy
030104 developmental biology
Oncology
030220 oncology & carcinogenesis
Tumor Escape
immunotherapy
business
Subjects
Details
- Language :
- English
- ISSN :
- 20953941
- Volume :
- 18
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Cancer Biology & Medicine
- Accession number :
- edsair.doi.dedup.....9e6d2dde283039022e09555d9693d80a