免疫组化检测乳腺癌中syndecan-1的价值

Q4 Medicine Libri Oncologici Pub Date : 2021-05-25 DOI:10.20471/LO.2021.49.01.04
Ivana Miše
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引用次数: 0

摘要

Syndecan-1(Sdc1)是一种跨膜硫酸乙酰肝素蛋白多糖,一种细胞外基质受体和细胞基质粘附组织者,包括在所有细胞接触表面的粘附中。它整合不同的细胞信号和生长因子之间的信号,并调节细胞增殖、致癌、迁移和血管生成。细胞运动和入侵首先需要失去Sdc1。Sdc1表达在细胞改变形状或位置前不久丧失,这降低了粘附性,但增强了细胞的移动性及其侵袭潜力。Sdc1从细胞表面的释放(脱落)使肿瘤生长和转移成为可能。Sdc1表达的这种变化对于侵袭性乳腺癌向转移表型的转变具有至关重要的价值,并且它是上皮向间充质转变(EMT)的一部分。EMT中包含的分子是抗癌药物治疗和控制肿瘤转移的潜在靶点。从不溶性(膜结合辅助感受器)到可溶性Sdc1的蛋白水解转化可能触发癌症增殖期转变为侵袭期,这也可能具有潜在的诊断和治疗益处。基质Sdc1的表达不仅意味着将从上皮细胞释放的Sdc1简单固定到基质上,还意味着在反应性基质成纤维细胞中原位合成Sdc1。通过与肝素结合生长因子相互作用,Sdc1在基质中积累,并有助于侵袭性肿瘤基质的增殖和新生血管生成。在70%以上的乳腺癌中,Sdc1是在基质成纤维细胞中诱导的,其在恶性和非恶性乳腺组织的基质中的表达存在显著差异。尽管部分乳腺癌失去了Sdc1,但在大多数乳腺癌中,Sdc1表达或过度表达,其表达与这种癌症对化疗的不良反应有关。关于Sdc1在癌症中的预后意义的研究显示了不平等的结果,这意味着需要对这一主题进行新的研究。
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Value of immunohistochemical determination of syndecan-1 in breast cancer
Syndecan-1 (Sdc1) is a transmembrane heparan-sulfate proteoglycan, an extracellular matrix receptor and a cell-matrix adhesion organiser, included in adhesion of all cell’s contact surfaces. It integrates different cellular signals and signals between growth factors, and modulates cell proliferation, carcinogenesis, migration and angiogenesis. Cellular motion and invasion first require loss of the Sdc1. Sdc1 expression is lost shortly before the cell changes shape or location, which decrease adhesiveness but enhance cellular mobility and their invasive potential. Releasing of Sdc1 from the cell surface (shedding) enables tumor growth and metastasizing. Such change of the Sdc1 expression is of crucial value for transition of invasive breast carcinoma to metastatic phenotype, and it is a part of epithelial-to-mesenchymal transition (EMT). Molecules included in EMT are potential targets for anticancer pharmacotherapy and control of tumor metastasizing. Maybe proteolytic conversion from insoluble (membrane bound coreceptor) to soluble Sdc1 is trigger for turning of proliferative phase of breast cancer to invasive one, which can also be of potential diagnostic-therapeutic benefit. Stromal Sdc1 expression means not merely the simple fixation of the released Sdc1 from the epithelial cells to the stromal, but also autochthonous Sdc1 synthesis in reactive stromal fibroblasts. By interacting with heparin-binding growth factors, Sdc1 accumulates in the stroma and can contribute to proliferation of invasive tumor stroma and neoangiogenesis. In more than 70% of breast carcinomas Sdc1 is induced in stromal fibroblasts, with the significant difference in its expression between stroma of malignant and non-malignant breast tissue. Although part of breast cancers loses Sdc1, in most of them it is expressed or over-expressed, and its expression is associated with a poorer response of this cancer to chemotherapy. Studies about prognostic significance of Sdc1 in breast cancer have shown unequal results, which refers to the need for new researches on this subject.
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来源期刊
Libri Oncologici
Libri Oncologici Medicine-Oncology
CiteScore
0.30
自引率
0.00%
发文量
9
审稿时长
8 weeks
期刊介绍: - Genitourinary cancer: the potential role of imaging - Hemoglobin level and neoadjuvant chemoradiation in patients with locally advanced cervical carcinoma
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