Hsa_Circ_002144通过miR-326/PKM轴促进糖酵解和乳腺癌的免疫逃逸

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yong Yang, Tianhao Xie, Peng Gao, Weijun Han, Yuhong Liu, Yanmei Wang
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引用次数: 0

摘要

背景:乳腺癌是全球女性因癌症死亡的主要原因之一,对女性健康构成重大威胁。因此,为乳腺癌患者寻找新的治疗靶点和预后生物标志物至关重要。研究方法采用生物信息学分析、定量实时 PCR(qRT-PCR)和荧光原位杂交(FISH)等方法研究 hsa_circ_002144 在乳腺癌中的表达。此外,还利用Transwell试验、Western印迹和细胞活力试验评估了hsa_circ_002144对乳腺癌细胞增殖、迁移和侵袭的影响。此外,还建立了一个小鼠模型来验证其功能。采用流式细胞术、WB 分析、酶联免疫吸附试验(ELISA)、qRT-PCR、外泌体分离和共培养系统来阐明巨噬细胞极化的分子机制。结果:我们首次发现了 hsa_circ_002144 在乳腺癌中的高表达。它影响肿瘤的生长和转移,并能通过糖酵解途径影响巨噬细胞的极化。结论这一发现为乳腺癌的治疗和预后评估提供了新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hsa_Circ_002144 Promotes Glycolysis and Immune Escape of Breast Cancer Through miR-326/PKM Axis.

Background: Breast cancer is a leading cause of cancer-related deaths in women worldwide, posing a significant threat to female health. Therefore, it is crucial to search for new therapeutic targets and prognostic biomarkers for breast cancer patients. Method: Bioinformatics analysis, quantitative real-time PCR (qRT-PCR), and fluorescence in situ hybridization (FISH) were employed to investigate the expression of hsa_circ_002144 in breast cancer. Transwell assay, Western blotting, and cell viability assay were utilized to assess the impact of hsa_circ_002144 on the proliferation, migration, and invasion of breast cancer cells. Additionally, a mouse model was established to validate its functionality. Flow cytometry, WB analysis, enzyme-linked immunosorbent assay (ELISA), qRT-PCR, exosomes isolation, and co-culture system were employed to elucidate the molecular mechanism underlying macrophage polarization. Result: we have discovered for the first time that hsa_circ_002144 is highly expressed in breast cancer. It affected tumor growth and metastasis and could influence macrophage polarization through the glycolytic pathway. Conclusion: This finding provides a new direction for breast cancer treatment and prognosis assessment.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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