Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/81524
Title: Dynamics of oxygen level-driven regulators in modulating autophagy in colorectal cancer cells
Authors: Tam, SY 
Wu, VWC 
Law, HKW 
Keywords: Autophagy
Autophagy regulator
Colorectal cancer cell
Hypoxia
Oxygen level
Issue Date: 2019
Publisher: Elsevier
Source: Biochemical and biophysical research communications, 2019, v. 517, no. 2, p. 193-200 How to cite?
Journal: Biochemical and biophysical research communications 
Abstract: Colorectal cancer is a common cancer with metachronous distant metastases still threatening overall survival. Tumor oxygen level influences tumor radiosensitivity in relation to autophagy and apoptosis. The objective of this study is to evaluate the expression and interaction between multiple key regulators in different oxygen levels. Human colorectal adenocarcinoma HT-29 cells were cultured in 1% or 10% oxygen level and irradiated by 2 Gy with different incubation time. Autophagy key regulators, AMPK, HIFs and JNK were evaluated by Western blot. Sequential autophagy key regulator activation was observed in the order of AMPK, HIF-1α, HIF-2α and JNK. 10% oxygen level could promote autophagy with similar degree of autophagy activation as 1% oxygen level in 48-h while irradiation could slightly inhibit autophagy. The results of this study supported prior evaluation of oxygen level and autophagy regulators for improving treatment efficacy and indicated the possible directions in developing individualized radiotherapy by selective targeting of hypoxic regions.
URI: http://hdl.handle.net/10397/81524
ISSN: 0006-291X
EISSN: 1090-2104
DOI: 10.1016/j.bbrc.2019.07.043
Rights: © 2019 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
The following publication Tam, S. Y., Wu, V. W., & Law, H. K. (2019). Dynamics of oxygen level-driven regulators in modulating autophagy in colorectal cancer cells. Biochemical and biophysical research communications, 517(2), 193-200 is available at https://doi.org/10.1016/j.bbrc.2019.07.043
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