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PTEN靶向PDK1调控肾透明细胞癌恶性生物学表型的作用机制研究

段霜霜 古丽乃再尔·阿卜杜赛麦提 张丽君 孙淼 柳惠斌

中国癌症杂志2025,Vol.35Issue(8):761-768,8.
中国癌症杂志2025,Vol.35Issue(8):761-768,8.DOI:10.19401/j.cnki.1007-3639.2025.08.004

PTEN靶向PDK1调控肾透明细胞癌恶性生物学表型的作用机制研究

Mechanisms of PTEN-regulated PDK1 in modulating malignant phenotypes of clear cell renal cell carcinoma

段霜霜 1古丽乃再尔·阿卜杜赛麦提 1张丽君 1孙淼 1柳惠斌2

作者信息

  • 1. 新疆医科大学药学院,新疆 乌鲁木齐 830000
  • 2. 新疆医科大学附属肿瘤医院药物临床试验机构,新疆 乌鲁木齐 830000
  • 折叠

摘要

Abstract

Background and purpose:The aberrant activation of pyruvate dehydrogenase kinase 1(PDK1)drives tumor microenvironment remodeling and metastasis through mediating the Warburg effect.As a critical tumor-suppressive phosphatase,phosphatase and tensin homolog deleted on chromoseme ten(PTEN)activates PDK1 via loss of expression to induce aerobic glycolysis and accelerate tumor progression.The molecular interplay between PDK1 and PTEN in kidney renal clear cell carcinoma(KIRC)urgently requires systematic elucidation.This study aimed to clarify how PTEN regulates PDK1 to inhibit malignant phenotypes in KIRC.Methods:Bioinformatics analysis was conducted to compare PTEN and PDK1 expression levels as well as their prognostic correlations in the Cancer Genome Atlas(TCGA)-KIRC datasets.KIRC cell models was established by either silencing PDK1 or enhancing its expression,subsequently evaluating their malignancy characteristics through cell counting kit-8(CCK-8)proliferation,colony formation,cell migration,and invasion assays.To validate the regulatory interactions,we used PDK1-overexpressing cells treated with a PTEN-specific inhibitor.Western blot was used to dectect the protein expression.Results:The TCGA-KIRC analysis found significantly higher mRNA levels of PTEN and PDK1 in tumor tissues compared to normal controls(P<0.05),yet this high expression was associated with improved overall survival(P<0.01).Besides,a strong positive correlation was observed between PTEN and PDK1 expressions(r=0.52,P<0.001).Functional assays demonstrated that PDK1 knockdown markedly promoted cell proliferation,migration,and invasion,whereas PDK1 overexpression exhibited opposing effects.Mechanistically,inhibiting PTEN worsened malignant behaviors(P<0.01),however,these effects were reversed by overexpressing PDK1.Conclusion:This study presents the first evidence of the dual tumor-suppressive function of the PTEN-PDK1 biological axis in renal cancer,which supports the development of precision treatment strategies based on novel targets.

关键词

肾透明细胞癌/PDK1/PTEN/分子机制/预后

Key words

Clear cell renal cell carcinoma/PDK1/PTEN/Molecular mechanisms/Prognosis

分类

医药卫生

引用本文复制引用

段霜霜,古丽乃再尔·阿卜杜赛麦提,张丽君,孙淼,柳惠斌..PTEN靶向PDK1调控肾透明细胞癌恶性生物学表型的作用机制研究[J].中国癌症杂志,2025,35(8):761-768,8.

基金项目

国家自然科学基金(2022D01C518). National Natural Science Foundation of China(2022D01C518). (2022D01C518)

中国癌症杂志

OA北大核心

1007-3639

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