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.
Keyphrases
- immune response
- mental health
- healthcare
- locally advanced
- insulin resistance
- blood glucose
- public health
- high intensity
- early stage
- papillary thyroid
- squamous cell carcinoma
- radiation therapy
- dendritic cells
- body mass index
- young adults
- risk assessment
- blood pressure
- squamous cell
- physical activity
- skeletal muscle
- weight gain
- mesenchymal stem cells
- cell therapy
- radiation induced
- weight loss
- human health
- health promotion
- childhood cancer
- chemotherapy induced