González-Borja Iranzu, Alors-Pérez Emilia, Amat Irene, Alonso Laura, Viyuela-García Cristina, Goñi Saioa, Reyes José C, Ceballos-Chávez María, Hernández-García Irene, Sánchez-Frías Marina E, Santamaría Enrique, Razquin Socorro, Arjona-Sánchez Álvaro, Arrazubi Virginia, Pérez-Sanz Jairo, Vera Ruth, Fernández-Irigoyen Joaquín, Castaño Justo P, Viúdez Antonio
OncobionaTras Lab, Navarrabiomed, Complejo Hospitalario de Navarra, Universidad Pública de Navarra, Instituto de Investigación Sanitaria de Navarra, Pamplona, Spain.
Hormones and Cancer Group, Maimonides Institute for Biomedical Research of Cordoba (IMIBIC), Córdoba, Spain.
Front Med (Lausanne). 2021 Nov 19;8:720128. doi: 10.3389/fmed.2021.720128. eCollection 2021.
Checkpoint with forkhead-associated and ring finger domains () has been proposed as a predictive and prognosis biomarker for different tumor types, but its role in pancreatic ductal adenocarcinoma (PDAC) remains unknown. The aim of this study was two-pronged: to review the role of in PDAC and evaluating as a potential predictive biomarker in this disease. For this purpose, we first explored the CHFR messenger (m)RNA expression and promoter methylation through the TCGA database. Secondly, the CHFR expression and promoter methylation were prospectively evaluated in a cohort of patients diagnosed with borderline ( = 19) or resectable ( = 16) PDAC by immunohistochemistry (IHC), methylation specific-PCR (MSP), and pyrosequencing. The results from the TCGA database showed significant differences in terms of progression-free survival (PFS) and overall survival (OS) based on the CHFR mRNA expression, which was likely independent from the promoter methylation. Importantly, our results showed that in primarily resected patients and also the entire cohort, a higher CHFR expression as indicated by the higher IHC staining intensity might identify patients with longer disease-free survival (DFS) and OS, respectively. Similarly, in the same cohorts, patients with lower methylation levels by pyrosequencing showed significantly longer OS than patients without this pattern. Both, the CHFR expression intensity and its promoter methylation were established as independent prognostic factors for PFS and OS in the entire cohort. In contrast, no significant differences were found between different methylation patterns for and the response to taxane-based neoadjuvant treatment. These results suggest the potential role of the higher expression of CHFR and the methylation pattern of its promoter as potential prognostic biomarkers in PDAC, thus warranting further comprehensive studies to extend and confirm our preliminary findings.
具有叉头相关结构域和环指结构域的检查点蛋白(CHFR)已被提出作为不同肿瘤类型的预测和预后生物标志物,但其在胰腺导管腺癌(PDAC)中的作用仍不清楚。本研究有两个目的:回顾CHFR在PDAC中的作用,并评估其作为该疾病潜在预测生物标志物的价值。为此,我们首先通过TCGA数据库探索CHFR信使核糖核酸(mRNA)表达和启动子甲基化情况。其次,通过免疫组织化学(IHC)、甲基化特异性聚合酶链反应(MSP)和焦磷酸测序,对一组诊断为临界性(n = 19)或可切除性(n = 16)PDAC的患者进行CHFR表达和启动子甲基化的前瞻性评估。TCGA数据库的结果显示,基于CHFR mRNA表达,无进展生存期(PFS)和总生存期(OS)存在显著差异,这可能与启动子甲基化无关。重要的是,我们的结果表明,在初次切除的患者以及整个队列中,免疫组织化学染色强度越高表明CHFR表达越高,这可能分别识别出无病生存期(DFS)和OS更长的患者。同样,在同一队列中,焦磷酸测序显示甲基化水平较低的患者的OS明显长于无此模式的患者。CHFR表达强度及其启动子甲基化均被确定为整个队列中PFS和OS的独立预后因素。相比之下,CHFR不同甲基化模式与基于紫杉烷的新辅助治疗反应之间未发现显著差异。这些结果表明,CHFR高表达及其启动子甲基化模式作为PDAC潜在的预后生物标志物具有潜在作用,因此有必要进行进一步的综合研究以扩展和证实我们的初步发现。