Rosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Department of Human Genetics, McGill University, Montreal, QC, Canada.
Oncogene. 2024 Jun;43(26):2015-2024. doi: 10.1038/s41388-024-03051-y. Epub 2024 May 14.
Somatic copy number alterations (SCNAs) are prevalent in cancer and play a significant role in both tumorigenesis and therapeutic resistance. While focal SCNAs have been extensively studied, the impact of larger arm-level SCNAs remains poorly understood. Here, we investigated the association between arm-level SCNAs and overall survival in triple-negative breast cancer (TNBC), an aggressive subtype of breast cancer lacking targeted therapies. We identified frequent arm-level SCNAs, including 21q gain and 7p gain, which correlated with poor overall survival in TNBC patients. Further, we identified the expression of specific genes within these SCNAs associated with survival. Notably, we found that the expression of RIPK4, a gene located on 21q, exhibited a strong correlation with poor overall survival. In functional assays, we demonstrated that targeting Ripk4 in a murine lung metastatic TNBC model significantly reduced tumor burden, improved survival, and increased CD4 and CD8 T cell infiltration. RIPK4 enhanced the survival of triple-negative breast cancer cells at secondary sites, thereby facilitating the formation of metastatic lesions. Our findings highlight the significance of arm-level SCNAs in breast cancer progression and identify RIPK4 as a putative driver of TNBC metastasis and immunosuppression.
体细胞拷贝数改变(SCNAs)在癌症中普遍存在,在肿瘤发生和治疗耐药性中发挥重要作用。虽然局灶性 SCNAs 已经得到了广泛研究,但更大臂级别的 SCNAs 的影响仍知之甚少。在这里,我们研究了臂级别的 SCNAs 与三阴性乳腺癌(TNBC)患者总体生存之间的关联,TNBC 是一种缺乏靶向治疗的侵袭性乳腺癌亚型。我们确定了频繁的臂级别的 SCNAs,包括 21q 增益和 7p 增益,它们与 TNBC 患者的总体生存不良相关。此外,我们还确定了这些 SCNAs 中与生存相关的特定基因的表达。值得注意的是,我们发现位于 21q 上的基因 RIPK4 的表达与总体生存不良具有很强的相关性。在功能测定中,我们证明了在鼠肺转移 TNBC 模型中靶向 Ripk4 可显著降低肿瘤负担、提高生存率并增加 CD4 和 CD8 T 细胞浸润。RIPK4 增强了三阴性乳腺癌细胞在次级部位的存活能力,从而促进了转移性病变的形成。我们的研究结果强调了臂级别的 SCNAs 在乳腺癌进展中的重要性,并确定 RIPK4 是 TNBC 转移和免疫抑制的潜在驱动因素。