High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy.
Hongbing MaShuyu ZhengXiaozhi ZhangTuotuo GongXin LvShenbo FuShuqun ZhangXiaoran YinJingcan HaoChangyou ShanShan HuangPublished in: Cell death & disease (2019)
Resistance to radiotherapy results in relapse and treatment failure in locally advanced esophageal squamous cell carcinoma (ESCC). High mobility group box 1 (HMGB1) is reported to be associated with the radioresistance in bladder and breast cancer. However, the role of HMGB1 in the radiotherapy response in ESCC has not been fully elucidated. Here, we investigated the role of HMGB1 to radioresistance in ESCC clinical samples and cell lines. We found that HMGB1 expression was associated with tumor recurrence after postoperative radiotherapy in locally advanced ESCC patients. HMGB1 knockdown in ESCC cells resulted in increased radiosensitivity both in vitro and in vivo. Autophagy level was found depressed in HMGB1 inhibition cells and activation of autophagy brought back cell's radioresistance. Our results demonstrate that HMGB1 activate autophagy and consequently promote radioresistance. HMGB1 may be used as a predictor of poor response to radiotherapy in ESCC patients. Our finding also highlights the importance of the utility of HMGB1 in ESCC radiosensitization.
Keyphrases
- locally advanced
- cell death
- induced apoptosis
- endoplasmic reticulum stress
- rectal cancer
- early stage
- end stage renal disease
- squamous cell carcinoma
- radiation therapy
- signaling pathway
- neoadjuvant chemotherapy
- dna damage response
- oxidative stress
- cell cycle arrest
- ejection fraction
- newly diagnosed
- chronic kidney disease
- radiation induced
- prognostic factors
- transcription factor
- phase ii study
- binding protein
- spinal cord injury
- poor prognosis
- patients undergoing
- single cell
- patient reported outcomes
- study protocol
- young adults
- dna damage
- mesenchymal stem cells
- lymph node