Recent advances in exploring new blood-based biomarkers for the early diagnosis of gastric cancer

被引:0
作者
Peng, Xinyu [1 ,2 ]
Ma, Qian [3 ]
Han, Da [1 ,2 ]
机构
[1] Shanghai Univ, Sch Life Sci, Shanghai 200444, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Key Lab Nucl Acid Chem & Nanomed, State Key Lab Oncogenes & Related Genes, Renji Hosp,Sch Med,Inst Mol Med, Shanghai 200127, Peoples R China
[3] Intellinosis Biotechnol Co Ltd, Dept Res & Dev, Shanghai 201112, Peoples R China
关键词
gastric cancer; early diagnosis; blood; CIRCULATING TUMOR-CELLS; LONG NONCODING RNAS; MESSENGER-RNA; CLINICAL-SIGNIFICANCE; EXTRACELLULAR VESICLES; POTENTIAL BIOMARKER; DNA METHYLATION; PEPSINOGEN TEST; LIQUID BIOPSY; RISK-FACTORS;
D O I
10.1007/s11426-024-2189-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gastric cancer (GC) is a prevalent and lethal malignancy worldwide, and the 5-year survival rate is less than 30%. The absence of distinctive symptoms often leads to late-stage diagnosis, contributing to a grim prognosis. Early detection is pivotal for improving the survival rates and outcomes of GC patients. Traditional diagnostic methods, including gastroscopy and histopathological examination, are restricted in the early diagnosis of GC. Conventional protein biomarkers, such as carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA19-9), and carbohydrate antigen 72-4 (CA72-4), exhibit insufficient sensitivity and specificity for GC screening, which diminishes their clinical value. Recently, novel circulating biomarkers, such as circulating tumor cells (CTCs), circulating tumor cell DNA (ctDNA), and circulating free RNA (cfRNA), have emerged as promising candidates in the burgeoning field of liquid biopsy due to their superior sensitivity and specificity. This review focuses on the latest research on blood-based biomarkers for GC diagnosis and examines the clinical potentials and challenges associated with these emerging biomarkers.
引用
收藏
页码:35 / 45
页数:11
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