Evaluation of Anti-Tumor Effects of Whole-Body Low-Dose Irradiation in Metastatic Mouse Models.
Kyung-Hee SongSeung-Youn JungJeong-In ParkJiyeon AhnJong-Kuk ParkSang-Gu HwangEun-Ho KimSeon Young NamSeungwoo ParkHunjoo HaJie-Young SongPublished in: Cancers (2020)
Low-dose irradiation (LDI) has recently been shown to have various beneficial effects on human health, such as on cellular metabolic activities, DNA repair, antioxidant activity, homeostasis potency, and immune activation. Although studies on the immunogenic effects of LDI are rapidly accumulating, clinical trials for cancer treatment are considered premature owing to the lack of available preclinical results and protocols. Here, we aim to investigate anti-tumor and anti-metastatic effects of whole-body LDI in several tumor-bearing mouse models. Mice were exposed to single or fractionated whole-body LDI prior to tumor transplantation, and tumor growth and metastatic potential were determined, along with analysis of immune cell populations and expression of epithelial-mesenchymal transition (EMT) markers. Whole-body fractionated-LDI decreased tumor development and lung metastasis not only by infiltration of CD4+, CD8+ T-cells, and dendritic cells (DCs) but also by attenuating EMT. Moreover, a combination of whole-body LDI with localized high-dose radiation therapy reduced the non-irradiated abscopal tumor growth and increased infiltration of effector T cells and DCs. Therefore, whole-body LDI in combination with high-dose radiation therapy could be a potential therapeutic strategy for treating cancer.
Keyphrases
- high dose
- low dose
- epithelial mesenchymal transition
- radiation therapy
- dendritic cells
- human health
- dna repair
- clinical trial
- small cell lung cancer
- squamous cell carcinoma
- risk assessment
- mouse model
- stem cell transplantation
- dna damage
- climate change
- metabolic syndrome
- poor prognosis
- signaling pathway
- radiation induced
- type diabetes
- randomized controlled trial
- stem cells
- regulatory t cells
- papillary thyroid
- long non coding rna
- rectal cancer
- insulin resistance
- squamous cell
- study protocol
- phase iii