The activation of EP300 by F11R leads to EMT and acts as a prognostic factor in triple-negative breast cancers

IF 3.4 2区 医学 Q1 PATHOLOGY
Chien-Hsiu Li, Chih-Yeu Fang, Ming-Hsien Chan, Pei-Jung Lu, Luo-Ping Ger, Jan-Show Chu, Yu-Chan Chang, Chi-Long Chen, Michael Hsiao
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引用次数: 1

Abstract

Cancer progression is influenced by junctional adhesion molecule (JAM) family members. The relationship between JAM family members and different types of cancer was examined using The Cancer Genome Atlas dataset. mRNA levels of the F11R (F11 receptor) in tumours were inversely correlated to the expression of JAM-2 and JAM-3. This relationship was unique to breast cancer (BCa) and was associated with poor prognosis (p = 0.024, hazard ratio = 1.44 [1.05–1.99]). A 50-gene molecular signature (prediction analysis of microarray 50) was used to subtype BCa. F11R mRNA expression significantly increased in human epidermal growth factor receptor 2 (HER2)-enriched (p = 0.0035) and basal-like BCa tumours (p = 0.0005). We evaluated F11R protein levels in two different compositions of BCa subtype patient tissue array cohorts to determine the relationship between BCa subtype and prognosis. Immunohistochemistry staining revealed that a high F11R protein level was associated with poor overall survival (p < 0.001; Taipei Medical University [TMU] cohort, p < 0.001; Kaohsiung Veterans General Hospital [KVGH] cohort) or disease-free survival (p < 0.001 [TMU cohort], p = 0.034 [KVGH cohort]) in patients with BCa. Comparison of F11R levels in different subtypes revealed the association of poor prognosis with high levels of F11R among luminal (p < 0.001 [TMU cohort], p = 0.027 [KVGH cohort]), HER2 positive (p = 0.018 [TMU cohort], p = 0.037 [KVGH cohort]), and triple-negative (p = 0.013 [TMU cohort], p = 0.037 [KVGH cohort]) BCa. F11R-based RNA microarray analysis and Ingenuity Pathway Analysis were successful in profiling the detailed gene ontology of triple-negative BCa cells regulated by F11R. The EP300 transcription factor was highly correlated with F11R in BCa (R = 0.51, p < 0.001). By analysing these F11R-affected molecules with the L1000CDs datasets, we were able to predict some repurposing drugs for potential application in F11R-positive BCa treatment.

Abstract Image

F11R激活EP300导致EMT,并作为三阴性乳腺癌的预后因素
肿瘤进展受连接粘附分子(JAM)家族成员的影响。JAM家族成员与不同类型癌症之间的关系使用癌症基因组图谱数据集进行了检查。肿瘤中F11R (F11受体)的mRNA水平与JAM-2和JAM-3的表达呈负相关。这种关系仅存在于乳腺癌(BCa)中,且与预后不良相关(p = 0.024,风险比= 1.44[1.05-1.99])。采用50基因分子标记(微阵列50预测分析)对BCa亚型进行分型。F11R mRNA在人表皮生长因子受体2 (HER2)富集(p = 0.0035)和基底样BCa肿瘤中表达显著升高(p = 0.0005)。我们评估了两种不同组成的BCa亚型患者组织阵列队列中的F11R蛋白水平,以确定BCa亚型与预后之间的关系。免疫组织化学染色显示,高水平的F11R蛋白与较差的总生存率相关(p < 0.001;台北医科大学队列,p < 0.001;高雄退伍军人总医院[KVGH]队列)或无病生存率(p < 0.001 [TMU队列],p = 0.034 [KVGH队列])。不同亚型患者F11R水平的比较显示,在luminal (p < 0.001 [TMU队列],p = 0.027 [KVGH队列])、HER2阳性(p = 0.018 [TMU队列],p = 0.037 [KVGH队列])、三阴性(p = 0.013 [TMU队列],p = 0.037 [KVGH队列])BCa中,F11R水平高与预后相关。基于F11R的RNA微阵列分析和匠心通路分析成功地描绘了F11R调控的三阴性BCa细胞的详细基因本体。BCa中EP300转录因子与F11R高度相关(R = 0.51, p < 0.001)。通过使用L1000CDs数据集分析这些受f11r影响的分子,我们能够预测一些可能用于f11r阳性BCa治疗的再利用药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pathology Clinical Research
Journal of Pathology Clinical Research Medicine-Pathology and Forensic Medicine
CiteScore
7.40
自引率
2.40%
发文量
47
审稿时长
20 weeks
期刊介绍: The Journal of Pathology: Clinical Research and The Journal of Pathology serve as translational bridges between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The focus of The Journal of Pathology: Clinical Research is the publication of studies that illuminate the clinical relevance of research in the broad area of the study of disease. Appropriately powered and validated studies with novel diagnostic, prognostic and predictive significance, and biomarker discover and validation, will be welcomed. Studies with a predominantly mechanistic basis will be more appropriate for the companion Journal of Pathology.
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