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缺氧和转录因子 HIF-1α 及 JMJD1A 水平对头颈部鳞状细胞癌细胞系上皮-间充质转化的影响。

Impact of Hypoxia and the Levels of Transcription Factor HIF-1α and JMJD1A on Epithelial-Mesenchymal Transition in Head and Neck Squamous Cell Carcinoma Cell Lines.

机构信息

Department of Oto-Rhino-Laryngology, Head and Neck Surgery, University Hospital Wuerzburg, Wuerzburg, Germany

Department of Oto-Rhino-Laryngology, Head and Neck Surgery, University Hospital Wuerzburg, Wuerzburg, Germany.

出版信息

Cancer Genomics Proteomics. 2024 Nov-Dec;21(6):591-607. doi: 10.21873/cgp.20476.

Abstract

BACKGROUND/AIM: This study aimed to assess the impact of hypoxia on epithelial-mesenchymal transition (EMT) in head and neck squamous cell carcinoma (HNSCC), focusing on the involvement of transcription factors hypoxia inducible factor 1 (HIF-1α) and Jumonji Domain-Containing Protein 1A (JMJD1A).

MATERIALS AND METHODS

FaDu and Cal33 cell lines were subjected to hypoxic and normoxic conditions. Cell proliferation was quantified electronically, while PCR and western blot analyses were used to measure mRNA and protein levels of HIF-1α, JMJD1A, and EMT markers. EMT was further characterized through immunofluorescence, migration, and invasion assays.

RESULTS

Hypoxic conditions significantly reduced cell proliferation after 48 hours in both cell lines. HIF-1α mRNA levels increased initially during short-term hypoxia but declined thereafter, while JMJD1A mRNA levels showed a sustained increase with prolonged hypoxia. Western blot analysis revealed contrasting trends in protein levels. EMT marker expression varied markedly over time at both the mRNA and protein levels, suggesting EMT induction in hypoxia within 24 hours. Immunofluorescence, migration, and invasion assays supported these findings.

CONCLUSION

The study provides evidence of hypoxia-induced EMT in HNSCC, although conflicting results suggest a complex interplay among molecular regulators involved in this process.

摘要

背景/目的:本研究旨在评估缺氧对头颈鳞状细胞癌(HNSCC)上皮-间充质转化(EMT)的影响,重点关注转录因子缺氧诱导因子 1(HIF-1α)和含 Jumonji 结构域的蛋白 1A(JMJD1A)的参与。

材料和方法

FaDu 和 Cal33 细胞系分别置于缺氧和常氧条件下。电子细胞增殖定量检测,PCR 和 Western blot 分析用于测量 HIF-1α、JMJD1A 和 EMT 标志物的 mRNA 和蛋白水平。通过免疫荧光、迁移和侵袭实验进一步表征 EMT。

结果

在两种细胞系中,缺氧条件在 48 小时后均显著降低细胞增殖。HIF-1α mRNA 水平在短期缺氧时最初增加,但随后下降,而 JMJD1A mRNA 水平在长期缺氧时持续增加。Western blot 分析显示蛋白水平呈现相反的趋势。EMT 标志物的表达在 mRNA 和蛋白水平上随时间变化差异显著,提示在 24 小时内缺氧诱导 EMT。免疫荧光、迁移和侵袭实验支持这些发现。

结论

本研究提供了 HNSCC 中缺氧诱导 EMT 的证据,尽管存在矛盾的结果,但表明这一过程中涉及的分子调节剂之间存在复杂的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ea1/11534036/7e6671b47361/cgp-21-593-g0001.jpg

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