SOX13-mediated transcription of LRP11 enhances malignant properties of tumor cells and CD8+ T cell inactivation in breast cancer through the β-catenin/PD-L1 axis

IF 4.4 2区 生物学 Q2 CELL BIOLOGY
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Abstract

Background

High expression of low-density lipoprotein receptor related protein 11 (LRP11) has been associated with unfavorable prognosis of breast cancer (BC). This study explores the exact roles of LRP11 in BC progression and investigates the associated mechanism.

Methods

LRP11 expression in BC tissues and cells was determined by immunohistochemistry or RT-qPCR. LRP11 upregulation was induced in two human BC cell lines to investigate its impact on cell proliferation, migration, and invasion. Its regulation on immune activity was assessed by detecting PD-L1 protein levels and generating a co-culture system of cancer cells and CD8+ T cells. Mouse allograft tumor models were generated to analyze the function of LRP11 in tumorigenesis and immune activity in vivo. Gain-of-function assays of SRY-box transcription factor 13 (SOX13) were performed to investigate its function in development and immunosuppression of BC.

Results

LRP11 was found to be highly expressed in BC tissues and cells, presenting an association with unfavorable prognosis of patients. Artificial upregulation of LRP11 in BC cells triggered malignant properties of cells, enhancing β-catenin-mediated transcriptional activation of PD-L1, thus decreasing immune activity of the co-cultured CD8+ T cells. Consistently, LRP11 upregulation in mouse 4 T1 cells and promoted tumorigenesis and immune evasion in mice. SOX13 was found to bind the LRP11 promoter for transcriptional activation. Upregulation of SOX13 similarly promoted growth of BC cells and immunosuppression, with its oncogenic effects blocked by the additional LRP11 knockdown.

Conclusion

This study demonstrates that SOX13 is responsible for LRP11 transcription activation, leading to increased malignant phenotype of BC cells and diminished activity CD8+ T cells. This evidence highlights SOX13 and LRP11 as promising novel therapeutic targets to reduce malignant phenotype of BC cells and overcome immunosuppression.

Abstract Image

SOX13介导的LRP11转录通过β-catenin/PD-L1轴增强了肿瘤细胞的恶性特性和乳腺癌CD8+T细胞的失活。
背景:低密度脂蛋白受体相关蛋白11(LRP11)的高表达与乳腺癌(BC)的不良预后有关。本研究探讨了 LRP11 在乳腺癌进展中的确切作用,并研究了相关机制:方法:通过免疫组化或 RT-qPCR 检测 LRP11 在 BC 组织和细胞中的表达。在两种人类 BC 细胞系中诱导 LRP11 上调,研究其对细胞增殖、迁移和侵袭的影响。通过检测 PD-L1 蛋白水平和生成癌细胞与 CD8+ T 细胞的共培养系统,评估了 LRP11 对免疫活性的调节作用。为了分析 LRP11 在体内肿瘤发生和免疫活动中的功能,我们制作了小鼠异种移植肿瘤模型。对SRY-box转录因子13(SOX13)进行了功能增益分析,以研究其在BC的发育和免疫抑制中的功能:结果:研究发现 LRP11 在 BC 组织和细胞中高表达,与患者的不良预后有关。LRP11在BC细胞中的人为上调会激发细胞的恶性特性,增强β-catenin介导的PD-L1转录激活,从而降低共培养CD8+ T细胞的免疫活性。同样,LRP11 在小鼠 4 T1 细胞中上调,促进了小鼠的肿瘤发生和免疫逃避。研究发现,SOX13 可与 LRP11 启动子结合以激活转录。SOX13的上调同样促进了BC细胞的生长和免疫抑制,其致癌作用被额外的LRP11敲除所阻断:这项研究表明,SOX13是LRP11转录激活的原因,导致BC细胞恶性表型增加和CD8+ T细胞活性降低。这些证据表明,SOX13和LRP11是降低BC细胞恶性表型和克服免疫抑制的有希望的新型治疗靶点。
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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