Solano-Iturri Jon Danel, Errarte Peio, Etxezarraga María C, Echevarria Enrique, Angulo Javier, López José I, Larrinaga Gorka
Department of Anatomic Pathology, Donostia University Hospital, 20014 Donostia/San Sebastian, Spain.
Department of Medical-Surgical Specialities, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
Cancers (Basel). 2020 Nov 16;12(11):3393. doi: 10.3390/cancers12113393.
(1) Background: Renal cell carcinoma (RCC) is a heterogeneous and complex disease with only partial response to therapy, high incidence of metastasis and recurrences, and scarce reliable biomarkers indicative of progression and survival. Cancer-associated fibroblasts (CAFs) play an important role supporting and promoting renal cancer progression. (2) Methods: In this study, we analysed fibroblast activation protein-α (FAP) immunohistochemical expression and its soluble isoform (sFAP) in tumour tissues and plasma from 128 patients with renal tumours. (3) Results: FAP is expressed in the cell surface of CAFs of the tumour centre and infiltrating front from clear cell renal cell carcinomas (CCRCC, = 89), papillary renal cell carcinomas (PRCC, = 21), and chromophobe renal cell carcinomas (ChRCC, = 8), but not in the benign tumour renal oncocytoma (RO, = 10). A high expression of FAP and low levels sFAP are significantly associated with high tumour diameter, high grade, and high pT stage, lymph node invasion, development of early metastases, and worse 5-year cancer specific survival of CCRCC patients. (4) Conclusions: These findings corroborate the potential usefulness of FAP immunohistochemistry and plasma sFAP as a biomarker of CCRCC progression and point to CAF-related proteins as promising immunohistochemical biomarkers for the differential diagnosis of ChRCC and RO.
(1) 背景:肾细胞癌(RCC)是一种异质性和复杂性疾病,对治疗仅有部分反应,转移和复发发生率高,且缺乏可靠的指示疾病进展和生存的生物标志物。癌症相关成纤维细胞(CAFs)在支持和促进肾癌进展中起重要作用。(2) 方法:在本研究中,我们分析了128例肾肿瘤患者肿瘤组织和血浆中纤维母细胞活化蛋白-α(FAP)的免疫组化表达及其可溶性异构体(sFAP)。(3) 结果:FAP表达于透明细胞肾细胞癌(CCRCC,n = 89)、乳头状肾细胞癌(PRCC,n = 21)和嫌色细胞肾细胞癌(ChRCC,n = 8)肿瘤中心和浸润前沿的CAFs细胞表面,但在良性肿瘤肾嗜酸细胞瘤(RO,n = 10)中不表达。FAP高表达和低水平sFAP与CCRCC患者的高肿瘤直径、高分级、高pT分期、淋巴结侵犯、早期转移发生及较差的5年癌症特异性生存率显著相关。(4) 结论:这些发现证实了FAP免疫组化和血浆sFAP作为CCRCC进展生物标志物的潜在用途,并指出CAF相关蛋白作为ChRCC和RO鉴别诊断有前景的免疫组化生物标志物。