Department of Oncology, Huashan Hospital Fudan University, 12 Middle Urumqi Road, Shanghai, 200000, China.
Shanghai Medical College, Fudan University, Shanghai, 200032, China.
J Transl Med. 2024 Jul 29;22(1):689. doi: 10.1186/s12967-024-05488-x.
Lung cancer stands as the second most prevalent malignant neoplasm worldwide. Addressing the underlying mechanisms propelling the progression of non-small cell lung cancer is of paramount importance. In this study, we have elucidated the pivotal role of PHF12 in this context.
We harnessed clinical lung cancer tissue samples and non-small cell lung cancer cell lines to discern the expression pattern of PHF12. In vitro assays probing cell proliferation were conducted to substantiate the functional impact of PHF12. Furthermore, an in vivo Xenograft model was employed to dissect the role of PHF12. Employing ChIP assays and qRT-PCR, we delved into the intricate binding dynamics between PHF12 and HDAC1. Mechanistic insights into the PHF12-HDAC1 axis in lung cancer progression were pursued via RNA-seq and GSEA analyses.
Notably, PHF12 exhibited a substantial upregulation within tumor tissue, concomitant with its correlation to HDAC1. The trilogy of cell proliferation assays, transwell assays, and the Xenograft model collectively underscored the promoting influence of PHF12 on lung cancer proliferation, both in vitro and in vivo. The ChIP assay unveiled the transcriptional regulatory role of PHF12 in governing HDAC1 expression. This correlation extended to both mRNA and protein levels. PHF12 promotes NSCLC progression through regulating HDCA1 expression. Intriguingly, the rescue of function within NSCLC cell lines post PHF12 knockdown was achievable through HDAC1 overexpression. Additionally, our findings unveiled the capacity of the PHF12-HDAC1 axis to activate the EGFR/AKT signaling pathway, thereby further corroborating its significance in lung cancer progression.
Our study identified PHF12 as an oncogenic role in lung cancer proliferation and migration for the first time. PHF12 transcriptionally regulate HDAC1 and activate EGFR/AKT signaling pathway in NSCLC progression. PHF12 may serve as an important target in lung cancer therapy.
肺癌是全球第二大常见恶性肿瘤。阐明推动非小细胞肺癌进展的潜在机制至关重要。在本研究中,我们阐明了 PHF12 在这方面的关键作用。
我们利用临床肺癌组织样本和非小细胞肺癌细胞系来辨别 PHF12 的表达模式。进行体外细胞增殖探测实验以证实 PHF12 的功能影响。此外,我们还使用了体内 Xenograft 模型来剖析 PHF12 的作用。通过 ChIP 实验和 qRT-PCR,我们深入研究了 PHF12 和 HDAC1 之间复杂的结合动态。通过 RNA-seq 和 GSEA 分析,我们探讨了 PHF12-HDAC1 轴在肺癌进展中的机制见解。
值得注意的是,PHF12 在肿瘤组织中显著上调,同时与 HDAC1 相关。细胞增殖实验、transwell 实验和 Xenograft 模型的三联实验共同强调了 PHF12 对肺癌增殖的促进作用,无论是在体外还是体内。ChIP 实验揭示了 PHF12 在调节 HDAC1 表达方面的转录调控作用。这种相关性延伸到 mRNA 和蛋白质水平。PHF12 通过调节 HDCA1 表达促进 NSCLC 进展。有趣的是,在 PHF12 敲低后,通过 HDAC1 过表达可以挽救 NSCLC 细胞系的功能。此外,我们的研究结果还揭示了 PHF12-HDAC1 轴激活 EGFR/AKT 信号通路的能力,从而进一步证实了其在肺癌进展中的重要性。
我们的研究首次发现 PHF12 在肺癌增殖和迁移中发挥致癌作用。PHF12 转录调控 HDAC1 并激活 EGFR/AKT 信号通路在 NSCLC 进展中。PHF12 可能成为肺癌治疗的一个重要靶点。