New blood markers detection technology: A leap in the diagnosis of gastric cancer

被引:69
作者
Beeharry, Maneesh K. [1 ]
Liu, Wen-Tao [1 ]
Yan, Min [1 ]
Zhu, Zheng-Gang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Digest Surg, Key Lab Shanghai Gastr Neoplasms,Dept Surg, 197 Ruijin Rd II, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
Gastric cancer; Circulating tumor cells; Circulating tumor DNA; Proteomics; Biomarkers; Methylation; CIRCULATING TUMOR-CELLS; PROMOTER HYPERMETHYLATION; QUANTITATIVE-ANALYSIS; POTENTIAL BIOMARKERS; PROGNOSTIC VALUE; MULTIPLE GENES; BREAST-CANCER; FOLLOW-UP; FREE DNA; SERUM;
D O I
10.3748/wjg.v22.i3.1202
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Gastric cancer (GC) is still one of the malignant tumors with high morbidity and mortality in the world, with a 5-year survival rate of less than 30%. GC is often either asymptomatic or causes only nonspecific symptoms in its early stages, whereas when the symptoms manifest, the cancer has usually reached an advanced stage, which is one of the main causes of its relatively poor prognosis. Hence, the main focus of GC research has been on discovering new tools and technology to predict, screen and diagnose GC at an early stage which would prompt early treatment. With the tremendous advances in the OMICS technology, serum proteomics has been in the limelight of cancer research over the last few decades and has steered the development of several methods helping to understand the mechanisms underlying gastric carcinogenesis, resulting in the identification of a large number of molecular targets such as circulating tumor cells (CTCs), cell free DNA (cfDNA) and cell tumor DNA (ctDNA) and their sub-molecular components such as miRNA, that show great promise as GC biomarkers. In this review, we are underlying the recent breakthroughs about new blood markers technology for GC while scrutinizing the potential clinical use of CTCs, cfDNA, ctDNA and the role of the methylation of their sub-molecular components in the pathogenesis, diagnosis and management of GC.
引用
收藏
页码:1202 / 1212
页数:11
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