4.6 Article

Choline Kinase Alpha2 Promotes Lipid Droplet Lipolysis in Non-Small-Cell Lung Carcinoma

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FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.848483

关键词

non-small-cell lung cancer; lipid metabolism; choline kinase; phosphorylation; prognostic biomarker

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资金

  1. Ministry of Science and Technology of the People's Republic of China [2020YFA0803300]
  2. National Natural Science Foundation of China [82188102, 82030074, 82122053, 32100574]
  3. R&D Program of Beijing Municipal Education commission [KJZD20191002302]
  4. CAMS Initiative for Innovative Medicine [2021-1-I2M-012]
  5. Aiyou Foundation [KY201701]
  6. Natural Science Foundation of Shandong Province [ZR2020QH191]
  7. Zhejiang Natural Science Foundation-Key Project [LD21H160003]
  8. Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang [2019R01001]

向作者/读者索取更多资源

The study revealed that under glutamine deficiency, CHKα2 plays a critical role in lipolysis of lipid droplets in non-small-cell lung cancer, sustaining tumor cell survival and proliferation. Additionally, the expression levels of ACC pS79 and CHKα2 pS279 are closely associated with patients' prognosis, with combined values being more predictive of patient survival.
BackgroundRapid tumor growth inevitably results in energy stress, including deficiency of glutamine, a critical amino acid for tumor cell proliferation. However, whether glutamine deficiency allows tumor cells to use lipid droplets as an energy resource and the mechanism underlying this potential regulation remain unclear. MethodsWe purified lipid droplets from H322 and H358 human non-small-cell lung cancer (NSCLC) cells under glutamine deprivation conditions and performed immunoblotting to determine the binding of choline kinase (CHK) alpha 2 to lipid droplets. Immunofluorescence was used to quantify lipid droplet numbers and sizes. Immunoprecipitation and immunoblotting were performed to examine AMPK activation and CHK alpha 2 phosphorylation. Cellular fatty acid levels, mitochondrial acetyl coenzyme A and ATP production, and cell apoptosis and proliferation were measured. Immunohistochemical analyses were performed to determine the expression levels of ACC pS79 and CHK alpha 2 pS279 in tumor specimens from NSCLC patients. The prognostic value of ACC pS79 and CHK alpha 2 pS279 was assessed using the Kaplan-Meier method and Cox regression models. ResultsGlutamine deficiency induces AMPK-mediated CHK alpha 2 S279 phosphorylation, which promotes the binding of CHK alpha 2 to lipid droplets, resulting in recruitment of cytosolic lipase ATGL and autophagosomes and subsequent lipolysis of lipid droplets to sustain tumor cell survival and proliferation. In addition, the levels of ACC pS79 and CHK alpha S279 were much higher in human NSCLC specimens than in their adjacent normal tissues and positively correlated with each other. Notably, ACC pS79 and CHK alpha pS279 expression levels alone were associated with poor prognosis of NSCLC patients, and combined values of both phosphorylation levels were correlated with worse prognosis of the patients. ConclusionCHK alpha 2 plays a critical role in lipolysis of lipid droplets in NSCLC. ACC pS79 and CHK alpha 2 pS279 alone or in combination can be used as prognostic markers in NSCLC.

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