Yiling Jiang, Hailong Li, Sixuan Wu, Baohong Jiang, Lijun Zeng, Yuanbin Tang, Lunqi Luo, Lianjie Ouyang, Wei Du, Yuehua Li
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Functional studies included tumor growth assays, MOSPD1 suppression and overexpression experiments, and testing BC cell responses to anti-PD-L1 therapy.</p><p><strong>Results: </strong>MOSPD1 expression was significantly higher in BC samples than normal tissues, correlating with poor clinical outcomes in BC patients. MOSPD1 suppression inhibited tumor growth, while overexpression accelerated it. Silencing MOSPD1 enhanced BC cell sensitivity to anti-PD-L1 therapy and decreased Th2 cell activity. In vivo experiments supported these findings, showing the impact of MOSPD1 on tumor growth and response to therapy.</p><p><strong>Conclusions: </strong>Elevated MOSPD1 levels in BC suggest its potential as a biomarker for adverse outcomes. Targeting MOSPD1, particularly with anti-PD-L1 therapy, may effectively inhibit BC tumor growth and modulate immune responses. 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引用次数: 0
摘要
背景:含精子结构域的运动蛋白1(MOSPD1)与乳腺癌(BC)的病理生理学有关,但其确切作用仍不清楚。本研究旨在评估MOSPD1在乳腺癌与正常组织中的表达水平,并探讨其诊断潜力:方法:分析 MOSPD1 在 BC 和正常组织中的表达,并利用接收者操作特征分析进行诊断评估。采用免疫组化方法进行验证。功能研究包括肿瘤生长实验、MOSPD1抑制和过表达实验,以及测试BC细胞对抗PD-L1疗法的反应:结果:MOSPD1在BC样本中的表达明显高于正常组织,与BC患者的不良临床预后相关。抑制MOSPD1可抑制肿瘤生长,而过表达则会加速肿瘤生长。沉默MOSPD1可增强BC细胞对抗PD-L1疗法的敏感性,并降低Th2细胞的活性。体内实验支持了这些发现,显示了MOSPD1对肿瘤生长和治疗反应的影响:结论:BC 中 MOSPD1 水平的升高表明它有可能成为不良后果的生物标志物。以MOSPD1为靶点,尤其是使用抗PD-L1疗法,可有效抑制BC肿瘤的生长并调节免疫反应。这项研究强调了MOSPD1在BC病理生理学中的重要性,并突出了其作为治疗靶点的前景。
Deciphering MOSPD1's impact on breast cancer progression and therapeutic response.
Background: Motile Sperm Domain-Containing Protein 1 (MOSPD1) has been implicated in breast cancer (BC) pathophysiology, but its exact role remains unclear. This study aimed to assess MOSPD1 expression levels in BC versus normal tissues and investigate its diagnostic potential.
Methods: MOSPD1 expression was analyzed in BC and normal tissues, with Receiver Operating Characteristic analysis for diagnostic evaluation. Validation was performed using immunohistochemistry. Functional studies included tumor growth assays, MOSPD1 suppression and overexpression experiments, and testing BC cell responses to anti-PD-L1 therapy.
Results: MOSPD1 expression was significantly higher in BC samples than normal tissues, correlating with poor clinical outcomes in BC patients. MOSPD1 suppression inhibited tumor growth, while overexpression accelerated it. Silencing MOSPD1 enhanced BC cell sensitivity to anti-PD-L1 therapy and decreased Th2 cell activity. In vivo experiments supported these findings, showing the impact of MOSPD1 on tumor growth and response to therapy.
Conclusions: Elevated MOSPD1 levels in BC suggest its potential as a biomarker for adverse outcomes. Targeting MOSPD1, particularly with anti-PD-L1 therapy, may effectively inhibit BC tumor growth and modulate immune responses. This study emphasizes the significance of MOSPD1 in BC pathophysiology and highlights its promise as a therapeutic target.
期刊介绍:
Biology Direct serves the life science research community as an open access, peer-reviewed online journal, providing authors and readers with an alternative to the traditional model of peer review. Biology Direct considers original research articles, hypotheses, comments, discovery notes and reviews in subject areas currently identified as those most conducive to the open review approach, primarily those with a significant non-experimental component.