دورية أكاديمية

AMP‐activated protein kinase β1 or β2 deletion enhances colon cancer cell growth and tumorigenesis

التفاصيل البيبلوغرافية
العنوان: AMP‐activated protein kinase β1 or β2 deletion enhances colon cancer cell growth and tumorigenesis
المؤلفون: Shi Fuli, Tang Zhimin, Jiang Shanshan, Xiong Zhijuan, Zhang Wansi, Li Yuanjun, Lin Hui, Luo Zhijun, Ying Ying
المصدر: Acta Biochimica et Biophysica Sinica, Vol 54, Pp 1140-1147 (2022)
بيانات النشر: China Science Publishing & Media Ltd., 2022.
سنة النشر: 2022
المجموعة: LCC:Biochemistry
LCC:Genetics
مصطلحات موضوعية: AMPKβ1, AMPKβ2, Warburg effect, tumorigenesis, colon cancer, Biochemistry, QD415-436, Genetics, QH426-470
الوصف: Abnormal metabolism is a major hallmark of cancer and has been validated as a therapeutic target. Adenine monophosphate‐activated protein kinase (AMPK), an αβγ heterotrimer, performs essential functions in cancer progression due to its central role in maintaining the homeostasis of cellular energy. While the contributions of AMPKα and AMPKγ subunits to cancer development have been established, specific roles of AMPKβ1 and AMPKβ2 isoforms in cancer development are poorly understood. Here, we show the functions of AMPKβ1 and AMPKβ2 in colon cancer. Specifically, deletion of AMPKβ1 or AMPKβ2 leads to increased cell proliferation, colony formation, migration, and tumorigenesis in HCT116 and HT29 colon cancer cells. Interestingly, the AMPKβ1 and AMPKβ2 isoforms have slightly different effects on regulating cancer metabolism, as colon cancer cells with AMPKβ1 knockout showed decreased rates of glycolysis-related oxygen consumption, while AMPKβ2 deletion led to enhanced rates of oxygen consumption due to oxidative phosphorylation. These results demonstrate that functional AMPKβ1 and AMPKβ2 inhibit growth and tumorigenesis in colon cancer cells, suggesting their potential as effective targets for colon cancer therapy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1672-9145
Relation: https://doaj.org/toc/1672-9145
DOI: 10.3724/abbs.2022086
URL الوصول: https://doaj.org/article/5d87dadd7c71494795b69143356b85bf
رقم الأكسشن: edsdoj.5d87dadd7c71494795b69143356b85bf
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16729145
DOI:10.3724/abbs.2022086