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整合素αvβ6作为外阴鳞状细胞癌及相邻癌前病变肿瘤特异性成像的靶点

Integrin αvβ6 as a Target for Tumor-Specific Imaging of Vulvar Squamous Cell Carcinoma and Adjacent Premalignant Lesions.

作者信息

Huisman Bertine W, Cankat Merve, Bosse Tjalling, Vahrmeijer Alexander L, Rissmann Robert, Burggraaf Jacobus, Sier Cornelis F M, van Poelgeest Mariette I E

机构信息

Center for Human Drug Research, 2333 CL Leiden, The Netherlands.

Department of Gynecology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

出版信息

Cancers (Basel). 2021 Nov 29;13(23):6006. doi: 10.3390/cancers13236006.

Abstract

Surgical removal of vulvar squamous cell carcinoma (VSCC) is associated with significant morbidity and high recurrence rates. This is at least partially related to the limited visual ability to distinguish (pre)malignant from normal vulvar tissue. Illumination of neoplastic tissue based on fluorescent tracers, known as fluorescence-guided surgery (FGS), could help resect involved tissue and decrease ancillary mutilation. To evaluate potential targets for FGS in VSCC, immunohistochemistry was performed on paraffin-embedded premalignant (high grade squamous intraepithelial lesion and differentiated vulvar intraepithelial neoplasia) and VSCC (human papillomavirus (HPV)-dependent and -independent) tissue sections with healthy vulvar skin as controls. Sections were stained for integrin αvβ6, CAIX, CD44v6, EGFR, EpCAM, FRα, MRP1, MUC1 and uPAR. The expression of each marker was quantified using digital image analysis. H-scores were calculated and percentages positive cells, expression pattern, and biomarker localization were assessed. In addition, tumor-to-background ratios were established, which were highest for (pre)malignant vulvar tissues stained for integrin αvβ6. In conclusion, integrin αvβ6 allowed for the most robust discrimination of VSCCs and adjacent premalignant lesions compared to surrounding healthy tissue in immunohistochemically stained tissue sections. The use of an αvβ6 targeted near-infrared fluorescent probe for FGS of vulvar (pre)malignancies should be evaluated in future studies.

摘要

外阴鳞状细胞癌(VSCC)的手术切除会导致显著的发病率和高复发率。这至少部分与区分(癌)前病变和正常外阴组织的视觉能力有限有关。基于荧光示踪剂的肿瘤组织照明,即荧光引导手术(FGS),有助于切除受累组织并减少辅助性切除。为了评估VSCC中FGS的潜在靶点,我们对石蜡包埋的癌前病变(高级别鳞状上皮内病变和分化型外阴上皮内瘤变)和VSCC(人乳头瘤病毒(HPV)相关和非相关)组织切片进行了免疫组织化学分析,并以健康外阴皮肤作为对照。切片用整合素αvβ6、碳酸酐酶IX(CAIX)、CD44v6、表皮生长因子受体(EGFR)、上皮细胞黏附分子(EpCAM)、叶酸受体α(FRα)、多药耐药相关蛋白1(MRP1)、黏蛋白1(MUC1)和尿激酶型纤溶酶原激活物受体(uPAR)进行染色。使用数字图像分析对每个标志物的表达进行定量。计算H评分,并评估阳性细胞百分比、表达模式和生物标志物定位。此外,还确定了肿瘤与背景的比率,其中整合素αvβ6染色的(癌)前外阴组织的该比率最高。总之,与免疫组织化学染色组织切片中的周围健康组织相比,整合素αvβ6能够最有效地鉴别VSCC和相邻的癌前病变。未来的研究应评估使用靶向αvβ6的近红外荧光探针进行外阴(癌)前病变的FGS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/829e/8656970/93832ce109e0/cancers-13-06006-g001.jpg

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