Circulating mRNA Profiling in Esophageal Squamous Cell Carcinoma Identifies FAM84B As A Biomarker in Predicting Pathological Response to Neoadjuvant Chemoradiation
Journal
Scientific Reports
Journal Volume
5
Pages
10291
Date Issued
2015
Author(s)
Abstract
Esophageal cancer patients with pathological complete response (pCR) to neoadjuvant chemoradiation (CRT) have favorable outcomes. Currently, there was no reliable biomarker predicting the response to CRT. Perioperative circulating mRNA may be associated with prognosis, but its application for predicting treatment response is unclear. We prospectively assessed the value of circulating messenger RNA (mRNA) profiling in predicting pCR for esophageal squamous cell carcinoma (ESCC). Patients with ESCC completing CRT followed by surgery were enrolled for analysis. Venous peripheral blood was obtained before and after CRT, and total RNA was extracted for hybridization-based whole genome expression analysis and quantitative RT-PCR. We found circulating expression profiling was significantly altered after CRT. Altered FAM84B expression was significantly predictive of pCR. The decrease of serum FAM84B protein level after CRT was also associated with pCR. Immunohistochemistry and western blot confirmed that FAM84B protein was overexpressed in the majority of patients and ESCC cell lines. Furthermore, knockdown of FAM84B delayed tumor growth in ectopic xenografts. We demonstrated the decreased of circulating FAM84B mRNA and protein after neoadjuvant CRT may predict pCR, and FAM84B protein is overexpressed in ESCC. The potential of FAM84B as a novel predictive biomarker, and its biological functions deserve further investigation. ? 2015, Nature Publishing Group. All rights reserved.
SDGs
Other Subjects
FAM84B protein, human; messenger RNA; tumor marker; tumor protein; adult; aged; animal; blood; cancer staging; Carcinoma, Squamous Cell; chemoradiotherapy; cluster analysis; disease model; drug screening; Esophageal Neoplasms; female; gene expression profiling; gene expression regulation; genetics; human; male; middle aged; mouse; neoadjuvant therapy; pathology; prognosis; treatment outcome; tumor cell line; Adult; Aged; Animals; Biomarkers, Tumor; Carcinoma, Squamous Cell; Cell Line, Tumor; Chemoradiotherapy; Cluster Analysis; Disease Models, Animal; Esophageal Neoplasms; Female; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Humans; Male; Mice; Middle Aged; Neoadjuvant Therapy; Neoplasm Proteins; Neoplasm Staging; Prognosis; RNA, Messenger; Treatment Outcome; Xenograft Model Antitumor Assays
Publisher
Nature Publishing Group
Type
journal article