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环状 RNA LIFR-007 通过促进乳腺癌中 hnRNPA1 的核输出和 YAP 磷酸化减少肝转移。

circLIFR-007 reduces liver metastasis via promoting hnRNPA1 nuclear export and YAP phosphorylation in breast cancer.

机构信息

State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.

The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, China.

出版信息

Cancer Lett. 2024 Jun 28;592:216907. doi: 10.1016/j.canlet.2024.216907. Epub 2024 Apr 27.

Abstract

Cancer metastasis is the major cause of death in patients with breast cancer (BC). The liver is a common site of breast cancer metastasis, and the 5-year survival rate of patients with breast cancer liver metastases (BCLMs) is only about 8.5 %. CircRNAs are involved in a variety of cancer-related pathological behaviors, and their unique structure and resistance to RNA degradation enable them to serve as ideal diagnostic biomarkers and therapeutic targets. Therefore, it is important to investigate the role and molecular mechanism of circRNAs in cancer metastasis. CircLIFR-007 was identified as a critical circular RNA in BC metastasis by circRNAs microarray and qRT-PCR experiment. Cell function assays were performed to explore the effect of circLIFR-007 in breast cancer cells. Experiments in vivo validated the function of circLIFR-007. Several molecular assays were performed to investigate the underlying mechanisms. We found that circLIFR-007 acted as a negative controller in breast cancer liver metastasis. CircLIFR-007 upregulates the phosphorylation level of YAP by exporting hnRNPA1 to promote the combination between hnRNPA1 and YAP in the cytoplasm. Overexpression of circLIFR-007 suppressed the expression of liver metastasis-related proteins, SREBF1 and SNAI1, which were regulated by transcription factor YAP. Functionally, circLIFR-007 inhibits the proliferation and metastasis of breast cancer cells both in vivo and in vitro.

摘要

癌症转移是乳腺癌(BC)患者死亡的主要原因。肝脏是乳腺癌转移的常见部位,乳腺癌肝转移(BCLM)患者的 5 年生存率仅约为 8.5%。CircRNAs 参与多种与癌症相关的病理行为,其独特的结构和对 RNA 降解的抗性使它们成为理想的诊断生物标志物和治疗靶点。因此,研究 circRNAs 在癌症转移中的作用和分子机制非常重要。CircLIFR-007 通过 circRNAs 微阵列和 qRT-PCR 实验被鉴定为 BC 转移中的关键环状 RNA。进行细胞功能测定以探讨 circLIFR-007 在乳腺癌细胞中的作用。体内实验验证了 circLIFR-007 的功能。进行了几种分子测定以研究潜在的机制。我们发现 circLIFR-007 作为乳腺癌肝转移的负调控因子发挥作用。CircLIFR-007 通过输出 hnRNPA1 来上调 YAP 的磷酸化水平,从而促进 hnRNPA1 和 YAP 在细胞质中的结合。circLIFR-007 的过表达抑制了受转录因子 YAP 调节的肝转移相关蛋白 SREBF1 和 SNAI1 的表达。功能上,circLIFR-007 抑制了体内和体外乳腺癌细胞的增殖和转移。

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