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PGAM1 通过 cAMP/AMPK/CEBPB 通路调节 ASS1 促进乳腺癌的进展。

PGAM1 regulation of ASS1 contributes to the progression of breast cancer through the cAMP/AMPK/CEBPB pathway.

机构信息

Department of Immunology, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Cancer Immunology and Biotherapy, Tianjin's Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, China.

出版信息

Mol Oncol. 2022 Aug;16(15):2843-2860. doi: 10.1002/1878-0261.13259. Epub 2022 Jun 27.

Abstract

Phosphoglycerate mutase 1 (PGAM1) is a crucial glycolytic enzyme, and its expression status has been confirmed to be associated with tumor progression and metastasis. However, the precise role and other biological functions of PGAM1 remain unclear. Here, we report that PGAM1 expression is upregulated and related to poor prognosis in patients with breast cancer (BC). Functional experiments showed that knockdown of PGAM1 could suppress the proliferation, invasion, migration, and epithelial-mesenchymal transition of BC cells. Through RNA sequencing, we found that argininosuccinate synthase 1 (ASS1) expression was markedly upregulated in BC cells following PGAM1 knockdown, and it is required to suppress the malignant biological behavior of BC cells. Importantly, we demonstrated that PGAM1 negatively regulates ASS1 expression through the cAMP/AMPK/CEBPB axis. In vivo experiments further validated that PGAM1 promoted tumor growth in BC by altering ASS1 expression. Finally, immunohistochemical analysis showed that downregulated ASS1 levels were associated with PGAM1 expression and poor prognosis in patients with BC. Our study provides new insight into the regulatory mechanism of PGAM1-mediated BC progression that might shed new light on potential targets and combination therapeutic strategies for BC treatment.

摘要

磷酸甘油酸变位酶 1(PGAM1)是一种关键的糖酵解酶,其表达状态已被证实与肿瘤的进展和转移有关。然而,PGAM1 的确切作用和其他生物学功能仍不清楚。在这里,我们报告 PGAM1 的表达上调与乳腺癌(BC)患者的预后不良有关。功能实验表明,PGAM1 的敲低可抑制 BC 细胞的增殖、侵袭、迁移和上皮-间充质转化。通过 RNA 测序,我们发现 PGAM1 敲低后 BC 细胞中精氨琥珀酸合成酶 1(ASS1)的表达明显上调,而 ASS1 是抑制 BC 细胞恶性生物学行为所必需的。重要的是,我们证明了 PGAM1 通过 cAMP/AMPK/CEBPB 轴负调控 ASS1 的表达。体内实验进一步验证了 PGAM1 通过改变 ASS1 的表达促进了 BC 的肿瘤生长。最后,免疫组织化学分析表明,下调的 ASS1 水平与 BC 患者的 PGAM1 表达和预后不良有关。我们的研究为 PGAM1 介导的 BC 进展的调控机制提供了新的见解,可能为 BC 的治疗提供新的潜在靶点和联合治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f369/9348593/42ef67c6c925/MOL2-16-2843-g008.jpg

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