Sublethal irradiation promotes the metastatic potential of hepatocellular carcinoma cells.
Yulin CaoYuan YinXue WangZhifeng WuYuhang LiuFuzheng ZhangJunhua LinZhaohui HuangLeyuan ZhouPublished in: Cancer science (2020)
Radiotherapy (RT) represents one of the major treatment methods for cancers. However, many studies have observed that in descendant surviving tumor cells, sublethal irradiation can promote metastatic ability, which is closely related to the tumor microenvironment. We therefore investigated the functions and mechanisms of sublethal irradiated liver nonparenchymal cells (NPCs) in hepatocellular carcinoma (HCC). In this study, primary rat NPCs and McA-RH7777 hepatoma cells were irradiated with 6 Gy X-ray. Conditioned media (CM) from nonirradiated (SnonR), irradiated (SR), or irradiated plus radiosensitizer celecoxib-treated (S[R + D]) NPCs were collected and added to sublethal irradiated McA-RH7777 cells. We showed that CM from sublethal irradiated NPCs significantly promoted the migration and invasion ability of sublethal irradiated McA-RH7777 cells, which was reversed by celecoxib. The differentially expressed genes in differently treated McA-RH7777 cells were enriched mostly in the AMP-activated protein kinase/mammalian target of rapamycin (AMPK/mTOR) signaling pathway. SR increased the migration and invasion ability of HCC cells by inhibiting AMPK/mTOR signaling, which was enhanced by the AMPK inhibitor compound C and blocked by the AMPK activator GSK-621. Analyses of HCC tissues after neoadjuvant radiotherapy confirmed the effects of radiation on the AMPK/mTOR pathway. Cytokine antibody arrays and further functional investigations showed that matrix metalloproteinase-8 (MMP-8) partly mediates the promotion effects of SR on the migration and invasion ability of HCC cells by regulating AMPK/mTOR signaling. In summary, our data indicate that MMP-8 secreted by irradiated NPCs enhanced the migration and invasion of HCC by regulating AMPK/mTOR signaling, revealing a novel mechanism mediating sublethal irradiation-induced HCC metastasis at the level of the tumor microenvironment.
Keyphrases
- induced apoptosis
- signaling pathway
- cell cycle arrest
- protein kinase
- skeletal muscle
- cell proliferation
- endoplasmic reticulum stress
- squamous cell carcinoma
- small cell lung cancer
- pi k akt
- oxidative stress
- magnetic resonance imaging
- cell death
- computed tomography
- radiation therapy
- radiation induced
- rectal cancer
- magnetic resonance
- climate change
- locally advanced
- inflammatory response
- deep learning
- dna methylation
- endothelial cells
- diabetic rats
- nuclear factor