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丙酮酸脱氢酶激酶的表达模式可预测预后,并与透明细胞肾细胞癌的免疫耗竭相关。

The expression pattern of pyruvate dehydrogenase kinases predicts prognosis and correlates with immune exhaustion in clear cell renal cell carcinoma.

机构信息

Biomarkers in Cancer Unit, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.

Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway.

出版信息

Sci Rep. 2023 May 5;13(1):7339. doi: 10.1038/s41598-023-34087-x.

DOI:10.1038/s41598-023-34087-x
PMID:37147361
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10162970/
Abstract

Renal cancer cells constitute a paradigm of tumor cells with a glycolytic reprogramming which drives metabolic alterations favouring cell survival and transformation. We studied the expression and activity of pyruvate dehydrogenase kinases (PDK1-4), key enzymes of the energy metabolism, in renal cancer cells. We analysed the expression, subcellular distribution and clinicopathological correlations of PDK1-4 by immunohistochemistry of tumor tissue microarray samples from a cohort of 96 clear cell renal cell carcinoma (ccRCC) patients. Gene expression analysis was performed on whole tumor tissue sections of a subset of ccRCC samples. PDK2 and PDK3 protein expression in tumor cells correlated with lower patient overall survival, whereas PDK1 protein expression correlated with higher patient survival. Gene expression analysis revealed molecular association of PDK2 and PDK3 expression with PI3K signalling pathway, as well as with T cell infiltration and exhausted CD8 T cells. Inhibition of PDK by dichloroacetate in human renal cancer cell lines resulted in lower cell viability, which was accompanied by an increase in pAKT. Together, our findings suggest a differential role for PDK enzymes in ccRCC progression, and highlight PDK as actionable metabolic proteins in relation with PI3K signalling and exhausted CD8 T cells in ccRCC.

摘要

肾癌细胞是糖酵解重编程的肿瘤细胞范例,这种重编程促使代谢改变,有利于细胞存活和转化。我们研究了丙酮酸脱氢酶激酶(PDK1-4)在肾癌细胞中的表达和活性,PDK1-4 是能量代谢的关键酶。我们通过对 96 例透明细胞肾细胞癌(ccRCC)患者肿瘤组织微阵列样本的免疫组织化学分析,研究了 PDK1-4 的表达、亚细胞分布和临床病理相关性。我们对 ccRCC 样本的一部分进行了全肿瘤组织切片的基因表达分析。肿瘤细胞中 PDK2 和 PDK3 蛋白的表达与患者总生存期较短相关,而 PDK1 蛋白的表达与患者生存期较长相关。基因表达分析揭示了 PDK2 和 PDK3 表达与 PI3K 信号通路以及 T 细胞浸润和耗竭 CD8 T 细胞的分子关联。二氯乙酸抑制人肾癌细胞系中的 PDK 导致细胞活力降低,同时 AKT 的磷酸化增加。总之,我们的发现表明 PDK 酶在 ccRCC 进展中具有不同的作用,并强调 PDK 作为与 PI3K 信号和 ccRCC 中耗竭的 CD8 T 细胞相关的可操作代谢蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/f979235b3d08/41598_2023_34087_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/6eb398e4fe0e/41598_2023_34087_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/5db8de29ed3d/41598_2023_34087_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/9a4791e94273/41598_2023_34087_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/ecd7736c7dc7/41598_2023_34087_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/f979235b3d08/41598_2023_34087_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/6eb398e4fe0e/41598_2023_34087_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/5db8de29ed3d/41598_2023_34087_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/9a4791e94273/41598_2023_34087_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/ecd7736c7dc7/41598_2023_34087_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7417/10162970/f979235b3d08/41598_2023_34087_Fig5_HTML.jpg

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