The First Affiliated Hospital of University of South China, Hengyang, Hunan Province, China.
College of Chemistry and Materials Science, Hengyang Normal University, Hengyang, Hunan Province, China.
Kaohsiung J Med Sci. 2022 Sep;38(9):848-857. doi: 10.1002/kjm2.12573. Epub 2022 Jul 21.
Numerous long noncoding RNAs (lncRNAs) are abnormally expressed in breast cancer (BC), but the underlying mechanisms remain large unknown. Here, we aimed to investigate the functions and mechanisms of lncRNA cancer susceptibility candidate 9 (CASC9) in BC. Western blotting and quantitative real-time PCR (qRT-PCR) were performed to assess gene and protein expression, respectively. The proliferative and metastatic abilities of BC cells were tested by cell counting kit-8 and transwell assays, respectively. The formation of lymphatic vessels was detected by tube formation assay. Chromatin immunoprecipitation (ChIP) and dual luciferase reporter assays were performed to verify molecular interactions. CASC9 was found to be highly expressed in BC tissues and cell lines, and ectopic overexpression was positively associated with tumor volume, TNM stage, and lymph node metastasis. In addition, CASC9 silencing significantly inhibited the proliferation and invasion of BC cells, as well as BC-associated invasion and formation of lymphatic vessels of human dermal lymphatic endothelial cells. Mechanical studies demonstrated that CASC9 could be transcriptionally activated by STAT3 and elevate SOX4 expression by enhancing the acetylation of its promoter region. Our results illustrated that STAT3-activated CASC9 served as a tumor-promoting gene involved in promoting BC invasion and BC-associated formation of lymphatic vessels by upregulating SOX4 through altering H3K27ac level. This finding elucidated a new underlying network of CASC9 in the metastasis of BC.
许多长链非编码 RNA(lncRNA)在乳腺癌(BC)中异常表达,但潜在机制仍不清楚。在这里,我们旨在研究 lncRNA 癌症易感性候选物 9(CASC9)在 BC 中的功能和机制。通过 Western blot 和定量实时 PCR(qRT-PCR)分别评估基因和蛋白质表达。通过细胞计数试剂盒-8 和 Transwell 分析分别测试 BC 细胞的增殖和迁移能力。通过管形成测定检测淋巴管的形成。进行染色质免疫沉淀(ChIP)和双荧光素酶报告基因测定以验证分子相互作用。发现 CASC9 在 BC 组织和细胞系中高度表达,并且异位过表达与肿瘤体积、TNM 分期和淋巴结转移呈正相关。此外,CASC9 沉默显著抑制 BC 细胞的增殖和侵袭,以及 BC 相关的人真皮淋巴管内皮细胞的侵袭和淋巴管形成。机械研究表明,CASC9 可被 STAT3 转录激活,并通过增强其启动子区域的乙酰化来升高 SOX4 的表达。我们的研究结果表明,STAT3 激活的 CASC9 作为一种促进肿瘤的基因,通过改变 H3K27ac 水平,通过上调 SOX4 促进 BC 侵袭和 BC 相关的淋巴管形成。这一发现阐明了 CASC9 在 BC 转移中的新潜在网络。