Early Diagnostic Markers for Esophageal Squamous Cell Carcinoma: Copy Number Alteration Gene Identification and cfDNA Detection

被引:0
|
作者
Chen, Jiamin [1 ]
Liu, Xi [1 ]
Zhang, Zhihua [1 ]
Su, Ruibing [1 ]
Geng, Yiqun [2 ]
Guo, Yi [3 ]
Zhang, Yimin [4 ,5 ]
Su, Min [1 ]
机构
[1] Shantou Univ Med Coll, Inst Clin Pathol, Dept Pathol, Shantou, Peoples R China
[2] Shantou Univ, Med Coll, Affiliated Hosp 2, Dept Cardiol, Shantou, Peoples R China
[3] Shantou Univ, Med Coll, Dept Mol Biol, Shantou, Peoples R China
[4] Shantou Univ, Canc Hosp, Coll Med, Dept Endoscopy, Shantou, Peoples R China
[5] Shantou Cent Hosp, Clin Res Ctr, Shantou, Peoples R China
基金
中国国家自然科学基金;
关键词
liquid biopsy; precancerous lesion; targeted sequencing; copy number alteration; esophageal squamous cell carcinoma; CIRCULATING TUMOR DNA; PLASMA; SERUM; METASTASIS; MICRORNAS; PROFILE; MODELS;
D O I
10.1016/j.labinv.2024.102127
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The high mortality rate of esophageal squamous cell carcinoma (ESCC) is exacerbated by the absence of early diagnostic markers. The pronounced heterogeneity of mutations in ESCC renders copy number alterations (CNAs) more prevalent among patients. The identification of CNA genes within esophageal squamous dysplasia (ESD), a precancerous stage of ESCC, is crucial for advancing early detection efforts. Utilization of liquid biopsies via droplet-based digital PCR (ddPCR) offers a novel strategy for detecting incipient tumor traces. This study undertook a thorough investigation of CNA profiles across ESCC development stages, integrating data from existing databases and prior investigations to pinpoint and confirm CNA markers conducive to early detection of ESCC. Targeted sequencing was employed to select potential early detection genes, followed by the establishment of prediction models for ESCC early detection using ddPCR. Our analysis revealed widespread CNAs during the ESD stage, mirroring the CNA landscape observed in ESCC. A total of 40 CNA genes were identified as highly frequent in both ESCC and ESD lesions, through a comprehensive gene-level CNA analysis encompassing ESD and ESCC tissues, ESCC cell lines, and pan-cancer data sets. Subsequent validation of 5 candidate markers via ddPCR underscored the efficacy of combined predictive models encompassing PIK3CA, SOX2, EGFR, MYC, and CCND1 in early ESCC screening, as evidenced by the area-under-the-curve values exceeding 0.92 (P < .0001) across various detection contexts. The findings highlighted the significant utility of CNA genes in the early screening of ESCC, presenting robust models that could facilitate early detection, broadscale population screening, and adjunctive diagnosis. (c) 2024 United States & Canadian Academy of Pathology. Published by Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页数:13
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