不同肿瘤类型中 ROR1 蛋白表达的异质性特征

Cancers Pub Date : 2024-05-15 DOI:10.3390/cancers16101874
Maria Gabriela Raso, Elizve Barrientos Toro, Kurt Evans, Yasmeen Rizvi, Rossana Lazcano, Argun Akcakanat, Patrizia Sini, Francesca Trapani, Eva Johanna Madlener, Lorenz Waldmeier, Alexander J. Lazar, Funda Meric-Bernstam
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引用次数: 0

摘要

作为癌症治疗靶点,Wnt 受体 ROR1 引起了越来越多的关注。涉及该受体的几种治疗方法的研究正在进行中;然而,对 ROR1 组织表达的研究仍然不足。我们对大量多种肿瘤和组织学类型的 ROR1 蛋白表达进行了免疫组化分析。我们分析了 12 个匿名的多肿瘤组织微阵列(TMA),包括间皮瘤、食管癌、上消化道癌、子宫内膜样癌以及其他肿瘤类型。此外,我们还研究了 5 种不同肉瘤类型的 TMA 和 6 种从 19 个不同解剖部位和肿瘤组织学类型中提取的患者异种移植 (PDX) TMA。共评估了 1142 例不同组织学类型的患者病例和 140 例放置在 TMA 中的 PDX。病理学家评估了每个病例中 ROR1 阳性的肿瘤细胞百分比和染色强度。为了确定每种肿瘤类型的染色流行率,如果病例中有超过 1% 的肿瘤细胞显示 ROR1 染色,则该病例被视为阳性。我们的免疫组化检测结果显示,ROR1 的表达情况各不相同。间皮瘤(84.6%)、脂肪肉瘤(36.1%)、胃肠道间质瘤(33.3%)和子宫内膜样癌(28.9%)的 ROR1 表达率较高。其他组织学类型,如乳腺癌、肺癌、肾细胞癌、肝细胞癌、尿路上皮癌、结肠癌、胶质母细胞瘤、胆管癌和子宫肌瘤的 ROR1 总表达量较少,介于 0.9% 和 13% 之间。间质软骨肉瘤、横纹肌肉瘤和胃腺癌病例中未见 ROR1 表达。总体而言,ROR1在所调查的大多数肿瘤类型中的表达相对较少且较低;然而,ROR1在某些肿瘤类型(如胃食管GIST)中的表达较少但较高,这表明ROR1预筛可能更适用于这些适应症。此外,间皮瘤显示出频繁和高水平的ROR1表达,这代表了一种以前未曾认识到的治疗机会。这些发现有助于开发ROR1靶向疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heterogeneous Profile of ROR1 Protein Expression across Tumor Types
The Wnt receptor ROR1 has generated increased interest as a cancer therapeutic target. Research on several therapeutic approaches involving this receptor is ongoing; however, ROR1 tissue expression remains understudied. We performed an immunohistochemistry analysis of ROR1 protein expression in a large cohort of multiple tumor and histologic types. We analyzed 12 anonymized multi-tumor tissue microarrays (TMAs), including mesothelioma, esophageal and upper gastrointestinal carcinomas, and uterine endometrioid carcinoma, among other tumor types. Additionally, we studied 5 different sarcoma types of TMAs and 6 patient-derived xenografts (PDX) TMAs developed from 19 different anatomic sites and tumor histologic types. A total of 1142 patient cases from different histologic types and 140 PDXs placed in TMAs were evaluated. Pathologists assessed the percentage of tumor cells in each case that were positive for ROR1 and the intensity of staining. For determining the prevalence of staining for each tumor type, a case was considered positive if >1% of its tumor cells showed ROR1 staining. Our immunohistochemistry assays revealed a heterogeneous ROR1 expression profile. A high prevalence of ROR1 expression was found in mesothelioma (84.6%), liposarcoma (36.1%), gastrointestinal stromal tumors (33.3%), and uterine endometrioid carcinoma (28.9%). Other histologic types such as breast, lung, renal cell, hepatocellular, urothelial carcinoma, and colon carcinomas; glioblastoma; cholangiocarcinoma; and leiomyosarcoma showed less ROR1 overall expression, ranging between 0.9 and 13%. No ROR1 expression was seen in mesenchymal chondrosarcoma, rhabdomyosarcoma, or gastric adenocarcinoma cases. Overall, ROR1 expression was relatively infrequent and low in most tumor types investigated; however, ROR1 expression was infrequent but high in selected tumor types, such as gastroesophageal GIST, suggesting that ROR1 prescreening may be preferable for those indications. Further, mesothelioma exhibited frequent and high levels of ROR1 expression, which represents a previously unrecognized therapeutic opportunity. These findings can contribute to the development of ROR1-targeted therapies.
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