Metge Brandon J, Elbahoty Mohamed H, Elhamamsy Amr R, Popple Anne E, Papineni Bhavya, Samant Rajeev S, Shevde Lalita A
Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.
Birmingham VA Medical Center, Birmingham, AL, USA.
Cell Death Dis. 2025 Aug 22;16(1):638. doi: 10.1038/s41419-025-07963-9.
Metastasis is the leading cause of poor clinical outcomes in solid tumors; yet despite recent advances many of the driving factors of metastasis remain poorly understood. Tumor cells that successfully metastasize are subject to numerous stress points from intrinsic and extrinsic factors that the cell must overcome to survive and colonize a secondary site. The nucleolus, the site of ribosome biogenesis, serves as a central hub for sensing and responding to cellular stress and plays a crucial role in this process; furthermore, emerging evidence highlights the potential role of ribosome biogenesis in driving metastasis. To further elucidate the interplay between nucleolar function and metastasis, we performed a comprehensive analysis of nucleolar proteomes from primary and metastatic breast cancer cell lines and identified proteins differentially enriched in the nucleoli of metastatic cells, of which 48 showed statistically significant enrichment. Among these, S100A16 was the most significantly enriched nucleolar protein. Notably, chromatin immunoprecipitation mass spectrometry (ChIP-MS) revealed that S100A16 was associated at rDNA loci with RPA194, the catalytic subunit of RNA Polymerase I, indicating a role in rRNA biosynthesis. Functionally, loss of S100A16 disrupted RNA Polymerase I activation and subsequent rRNA synthesis, reversed epithelial-to-mesenchymal transition, inhibited invasion, and reduced metastatic incidence in animal models of breast cancer. Clinically, elevated S100A16 expression correlated with enrichment of ribosome biogenesis pathways and reduced relapse-free survival in metastatic breast cancer patients. In summary, we identified a critical role for S100A16 as a molecular modulator in the nucleolus that impinges upon breast cancer metastasis.
转移是实体瘤临床预后不良的主要原因;然而,尽管最近取得了进展,但许多转移的驱动因素仍知之甚少。成功转移的肿瘤细胞会受到来自内在和外在因素的众多应激点影响,细胞必须克服这些应激点才能在继发部位存活和定植。核仁是核糖体生物合成的场所,作为感知和应对细胞应激的中心枢纽,在这一过程中发挥着关键作用;此外,新出现的证据突出了核糖体生物合成在驱动转移中的潜在作用。为了进一步阐明核仁功能与转移之间的相互作用,我们对原发性和转移性乳腺癌细胞系的核仁蛋白质组进行了全面分析,确定了在转移细胞的核仁中差异富集的蛋白质,其中48种显示出统计学上的显著富集。其中,S100A16是最显著富集的核仁蛋白。值得注意的是,染色质免疫沉淀质谱分析(ChIP-MS)显示,S100A16在rDNA位点与RNA聚合酶I的催化亚基RPA194相关联,表明其在rRNA生物合成中发挥作用。在功能上,S100A16的缺失破坏了RNA聚合酶I的激活及随后的rRNA合成,逆转了上皮-间质转化,抑制了侵袭,并降低了乳腺癌动物模型中的转移发生率。在临床上,S100A16表达升高与核糖体生物合成途径的富集相关,并降低了转移性乳腺癌患者的无复发生存率。总之,我们确定了S100A16作为核仁中的分子调节因子在影响乳腺癌转移方面的关键作用。