Kim Jisup, Park Jee-Young, Shin Su-Jin, Lim Beom Jin, Go Heounjeong
Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Department of Pathology, Yonsei University College of Medicine, Seoul 03722, Korea.
Cancers (Basel). 2021 Mar 10;13(6):1199. doi: 10.3390/cancers13061199.
: Frameshift indels have emerged as a predictor of immunotherapy response but were not evaluated yet to predict anti-angiogenetic agent (AAA) response or prognosis in clear cell renal cell carcinoma (ccRCC). : Here, to develop biomarkers that predict survival and response to AAA, we evaluated the immunohistochemical expression of proteins whose genes frequently harbor frameshift indels in 638 ccRCC patients and correlated the individual and integrated markers with prognosis and AAA response. The mutational landscape was evaluated using targeted next-generation sequencing in 12 patients concerning protein markers. Immune gene signatures were retrieved from TCGA RNA seq data. : Five proteins (APC, NOTCH1, ARID1A, EYS, and filamin A) were independent adverse prognosticators and were incorporated into the Neo-fs index. Better overall, disease-specific and recurrence-free survival were observed with high Neo-fs index in univariate and multivariate survival analyses. Better AAA responses were observed with a high Neo-fs index, which reflected increased MHC class I, CD8+ T cell, cytolytic activity, and plasmacytoid dendritic cell signatures and decreased type II-IFN response signatures, as well as greater single-nucleotide variant (SNV) and indel counts. : Neo-fs index, reflecting antitumor immune signature and more SNVs. and indels, is a powerful predictor of survival and AAA response in ccRCC.
移码插入缺失已成为免疫治疗反应的预测指标,但尚未在透明细胞肾细胞癌(ccRCC)中评估其对抗血管生成药物(AAA)反应或预后的预测作用。在此,为了开发预测生存期和对AAA反应的生物标志物,我们评估了638例ccRCC患者中其基因经常存在移码插入缺失的蛋白质的免疫组化表达,并将个体和综合标志物与预后及AAA反应相关联。使用靶向二代测序对12例患者的蛋白质标志物进行了突变图谱评估。从TCGA RNA序列数据中获取免疫基因特征。五种蛋白质(APC、NOTCH1、ARID1A、EYS和细丝蛋白A)是独立的不良预后因素,并被纳入Neo-fs指数。在单变量和多变量生存分析中,Neo-fs指数高的患者总生存期、疾病特异性生存期和无复发生存期更好。Neo-fs指数高的患者对AAA反应更好,这反映了MHC I类、CD8 + T细胞、细胞溶解活性和浆细胞样树突状细胞特征增加,II型干扰素反应特征降低,以及单核苷酸变异(SNV)和插入缺失计数增加。Neo-fs指数反映了抗肿瘤免疫特征以及更多的SNV和插入缺失,是ccRCC生存期和AAA反应的有力预测指标。