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信号肽 CUB 域表皮生长因子样模体蛋白 3(SCUBE3)是乳腺癌独立的不良预后因素。

SCUBE3 serves as an independent poor prognostic factor in breast cancer.

作者信息

Huo Qin, He Xi, Li Zhenwei, Yang Fan, He Shengnan, Shao Ling, Hu Ye, Chen Siqi, Xie Ni

机构信息

Biobank, Institute of Translational Medicine, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen, 518035, China.

The Eighth Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518033, China.

出版信息

Cancer Cell Int. 2021 May 18;21(1):268. doi: 10.1186/s12935-021-01947-3.

Abstract

BACKGROUND

Accumulating evidences indicate that the signal peptide-CUB-EGF-like domain-containing protein 3 (SCUBE3) plays a key role in the development and progression of many human cancers. However, the underlying mechanism and prognosis value of SCUBE3 in breast cancer are still unclear.

METHODS

The clinical data of 137 patients with breast cancer who underwent surgical resection in Taizhou Hospital of Zhejiang Province were retrospectively analyzed. We first conducted a comprehensive study on the expression pattern of SCUBE3 using the Tumor Immune Estimation Resource (TIMER) and UALCAN databases. In addition, the expression of SCUBE3 in breast tumor tissues was confirmed by immunohistochemistry. The protein-protein interaction analysis and functional enrichment analysis of SCUBE3 were analyzed using the STRING and Enrichr databases. Moreover, tissue microarray (TMA) was used to analyze the relationship between SCUBE3 expression levels and clinical-pathological parameters, such as histological type, grade, the status of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor (HER2). We further supplemented and identified the above results using the UALCAN and bc-GenExMiner v4.4 databases from TCGA data. The correlation between the expression of SCUBE3 and survival was calculated by multivariate Cox regression analysis to investigate whether SCUBE3 expression may be an independent prognostic factor of breast cancer.

RESULTS

We found that the expression level of SCUBE3 was significantly upregulated in breast cancer tissue compared with adjacent normal tissues. The results showed that the distribution of breast cancer patients in the high expression group and the low expression group was significantly different in ER, PR, HER2, E-cadherin, and survival state (p < 0.05), but there was no significant difference in histologic grade, histologic type, tumor size, lymph node metastasis, TMN stage, subtypes, or recurrence (p > 0.05). In addition, the high expression of SCUBE3 was associated with relatively poor prognosis of ER- (p = 0.012), PR- (p = 0.029), HER2 + (p = 0.007). The multivariate Cox regression analysis showed that the hazard ratio (HR) was 2.80 (95% CI 1.20-6.51, p = 0.0168) in individuals with high SCUBE3 expression, and HR was increased by 1.86 (95% CI 1.06-3.25, p = 0.0300) for per 1-point increase of SCUBE3 expression.

CONCLUSIONS

These findings demonstrate that the high expression of SCUBE3 indicates poor prognosis in breast cancer. SCUBE3 expression may serve as a potential diagnostic indicator of breast cancer.

摘要

背景

越来越多的证据表明,含信号肽-CUB-EGF样结构域蛋白3(SCUBE3)在多种人类癌症的发生和发展中起关键作用。然而,SCUBE3在乳腺癌中的潜在机制和预后价值仍不清楚。

方法

回顾性分析浙江省台州医院137例行手术切除的乳腺癌患者的临床资料。我们首先使用肿瘤免疫评估资源(TIMER)和UALCAN数据库对SCUBE3的表达模式进行了全面研究。此外,通过免疫组织化学证实了SCUBE3在乳腺肿瘤组织中的表达。使用STRING和Enrichr数据库对SCUBE3进行蛋白质-蛋白质相互作用分析和功能富集分析。此外,组织芯片(TMA)用于分析SCUBE3表达水平与临床病理参数之间的关系,如组织学类型、分级、雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体(HER2)的状态。我们使用来自TCGA数据的UALCAN和bc-GenExMiner v4.4数据库进一步补充和验证上述结果。通过多因素Cox回归分析计算SCUBE3表达与生存之间的相关性,以研究SCUBE3表达是否可能是乳腺癌的独立预后因素。

结果

我们发现,与相邻正常组织相比,SCUBE3在乳腺癌组织中的表达水平显著上调。结果显示,高表达组和低表达组乳腺癌患者在ER、PR、HER2、E-钙黏蛋白和生存状态方面的分布有显著差异(p<0.05),但在组织学分级、组织学类型、肿瘤大小、淋巴结转移、TMN分期、亚型或复发方面无显著差异(p>0.05)。此外,SCUBE3的高表达与ER-(p=0.012)、PR-(p=0.029)、HER2+(p=0.007)患者相对较差的预后相关。多因素Cox回归分析显示,SCUBE3高表达个体的风险比(HR)为2.80(95%CI 1.20-6.51,p=0.0168),SCUBE3表达每增加1分,HR增加1.86(95%CI 1.06-3.25,p=0.0300)。

结论

这些发现表明,SCUBE3的高表达表明乳腺癌预后不良。SCUBE3表达可能作为乳腺癌的潜在诊断指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d200/8130162/dd9a48284b8f/12935_2021_1947_Fig1_HTML.jpg

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