AMPK promotes the survival of colorectal cancer stem cells
Title
AMPK promotes the survival of colorectal cancer stem cells
Date
2018
Publisher
Wiley
Subject
AMP‐activated protein kinase
Cancer metabolism
Colorectal cancer stem cells
Patient‐derived xenograft
Cancer metabolism
Colorectal cancer stem cells
Patient‐derived xenograft
Language
English
Abstract
Background
Colorectal cancer (CRC) is the third most commonly diagnosed cancer in males and the second in females worldwide in 2012. In the past 20 years, strong evidence suggests that cancer stem cells are the main culprit of cancer metastasis, chemotherapy resistance, and relapse.
Methods
To further understand the unique biological properties of cancer stem cells and uncover novel molecular targets to eradicate them, we first established a panel of patient-derived xenograft (PDX) tumor models using tumors surgically removed from human colorectal cancer patients. We then isolated CRC cancer stem cells based on their ALDH activity using fluorescent-activated cell sorting (FACS) and characterized their metabolic properties.
Results
Interestingly, we found that the CRC cancer stem cells (ie, CRC cells with higher ALDH activity, or ALDH+) express higher level of antioxidant genes and have lower level of reactive oxygen species (ROS) than non-CRC cancer stem cells (ie, CRC cells with lower ALDH activity, or ALDH−). The CRC cancer stem cells also possess more mitochondria mass and show higher mitochondrial activity. More intriguingly, we observed higher AMP-activated protein kinase (AMPK) activities in these CRC cancer stem cells. Inhibition of the AMPK activity using 2 AMPK inhibitors, Compound C and Iodotubercidin, preferentially induces cell death in CRC cancer stem cells.
Conclusion
We propose that AMPK inhibitors may help to eradicate the CRC cancer stem cells and prevent the relapse of CRCs.
Colorectal cancer (CRC) is the third most commonly diagnosed cancer in males and the second in females worldwide in 2012. In the past 20 years, strong evidence suggests that cancer stem cells are the main culprit of cancer metastasis, chemotherapy resistance, and relapse.
Methods
To further understand the unique biological properties of cancer stem cells and uncover novel molecular targets to eradicate them, we first established a panel of patient-derived xenograft (PDX) tumor models using tumors surgically removed from human colorectal cancer patients. We then isolated CRC cancer stem cells based on their ALDH activity using fluorescent-activated cell sorting (FACS) and characterized their metabolic properties.
Results
Interestingly, we found that the CRC cancer stem cells (ie, CRC cells with higher ALDH activity, or ALDH+) express higher level of antioxidant genes and have lower level of reactive oxygen species (ROS) than non-CRC cancer stem cells (ie, CRC cells with lower ALDH activity, or ALDH−). The CRC cancer stem cells also possess more mitochondria mass and show higher mitochondrial activity. More intriguingly, we observed higher AMP-activated protein kinase (AMPK) activities in these CRC cancer stem cells. Inhibition of the AMPK activity using 2 AMPK inhibitors, Compound C and Iodotubercidin, preferentially induces cell death in CRC cancer stem cells.
Conclusion
We propose that AMPK inhibitors may help to eradicate the CRC cancer stem cells and prevent the relapse of CRCs.
Source
Animal Models and Experimental Medicine, Volume 1, Issue 2, July 2018, pages 134-142
Rights
CC BY-NC 4.0 DEED Attribution-NonCommercial 4.0 International
Format
PDF
Type
Text
Identifier
Bibliographic Citation
Guo, B., Han, X., Tkach, D., Huang, S., & Zhang, D. (2018). AMPK promotes the survival of colorectal cancer stem cells. In Animal Models and Experimental Medicine (Vol. 1, Issue 2, pp. 134–142). Wiley. https://doi.org/10.1002/ame2.12016
Files
Collection
Citation
Guo, B., Han, X., Tkach, D., Huang, S., & Zhang, D., AMPK promotes the survival of colorectal cancer stem cells. Animal Models and Experimental Medicine, Volume 1, Issue 2, July 2018, pages 134-142, New York Tech Institutional Repository, accessed September 15, 2024, https://repository.nyitlibrary.org/items/show/3754
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