Histopathology, University of Nottingham School of Medicine, Nottingham, UK
Histopathology, University of Nottingham School of Medicine, Nottingham, UK.
J Clin Pathol. 2020 Feb;73(2):76-82. doi: 10.1136/jclinpath-2019-205939. Epub 2019 Aug 23.
Cathepsin V (CTSV/CTSL2) is a lysosomal cysteine proteinase and plays a role in extracellular matrix degradation. It is associated with poor prognosis in invasive breast cancer (IBC), but its role in breast ductal carcinoma in situ (DCIS) remains unclear. In this study, we aimed to evaluate the prognostic significance of CTSV in DCIS.
CTSV protein expression was immunohistochemically assessed in a well-characterised and annotated cohort of DCIS comprising pure DCIS (n=776) and DCIS coexisting with IBC (n=239). CTSV expression was analysed in tumour cells and surrounding stroma, including its association with clinicopathological parameters and outcome.
In pure DCIS, high CTSV expression was observed in 29% of epithelial tumour cells and 20% of surrounding stroma. High expression in both components was associated with features of poor prognosis including higher nuclear grade, hormone receptor negativity and HER2 positivity. In addition, stromal CTSV expression was associated with larger DCIS size, comedo-type necrosis and high proliferation index. DCIS associated with IBC showed higher CTSV expression than pure DCIS either within the epithelial tumour cells or surrounding stroma (p<0.0001 and p=0.001, respectively). In DCIS/IBC, CTSV expression was higher in the invasive component than DCIS component either in tumour cells or surrounding stroma (both p<0.0001). CTSV stromal expression was associated with invasive recurrence independent of other prognostic factors in patients treated with breast conserving surgery (HR=3.0, p=0.005).
High expression of CTSV is associated with poor outcome in DCIS and is a potential marker to predict DCIS progression to invasive disease.
组织蛋白酶 V(CTSV/CTSL2)是一种溶酶体半胱氨酸蛋白酶,在细胞外基质降解中发挥作用。它与浸润性乳腺癌(IBC)的不良预后相关,但在乳腺导管原位癌(DCIS)中的作用尚不清楚。在本研究中,我们旨在评估 CTSV 在 DCIS 中的预后意义。
使用经过充分特征描述和注释的 DCIS 队列进行免疫组织化学评估,该队列包括纯 DCIS(n=776)和与 IBC 共存的 DCIS(n=239)。分析 CTSV 表达在肿瘤细胞和周围基质中的情况,包括其与临床病理参数和结局的关系。
在纯 DCIS 中,29%的上皮肿瘤细胞和 20%的周围基质中观察到高 CTSV 表达。两种成分的高表达与预后不良的特征相关,包括核分级较高、激素受体阴性和 HER2 阳性。此外,基质 CTSV 表达与更大的 DCIS 大小、粉刺样坏死和高增殖指数相关。与纯 DCIS 相比,与 IBC 相关的 DCIS 在肿瘤细胞或周围基质中均表现出更高的 CTSV 表达(p<0.0001 和 p=0.001)。在 DCIS/IBC 中,无论是在肿瘤细胞还是周围基质中,侵袭性成分的 CTSV 表达均高于 DCIS 成分(两者均 p<0.0001)。在接受保乳手术治疗的患者中,基质 CTSV 表达与侵袭性复发相关,独立于其他预后因素(HR=3.0,p=0.005)。
CTSV 的高表达与 DCIS 的不良预后相关,是预测 DCIS 进展为侵袭性疾病的潜在标志物。