Circulating tumour DNA alterations: emerging biomarker in head and neck squamous cell carcinoma

被引:15
|
作者
Huang, Xiaomin [1 ]
Duijf, Pascal H. G. [2 ,3 ,4 ,5 ,6 ,7 ]
Sriram, Sharath [8 ]
Perera, Ganganath [8 ]
Vasani, Sarju [9 ,10 ]
Kenny, Lizbeth [10 ]
Leo, Paul [2 ,3 ,11 ]
Punyadeera, Chamindie [1 ,12 ]
机构
[1] Griffith Univ, Griffith Inst Drug Discovery GRIDD, Sch Environm & Sci, Saliva & Liquid Biopsy Translat Lab, Brisbane, Qld, Australia
[2] Queensland Univ Technol, Fac Hlth, Sch Biomed Sci, Brisbane, Qld, Australia
[3] Queensland Univ Technol, Ctr Genom & Personalised Hlth, Brisbane, Qld, Australia
[4] Queensland Univ Technol, Ctr Data Sci, Brisbane, Qld, Australia
[5] Univ Oslo, Inst Clin Med, Fac Med, Oslo, Norway
[6] Oslo Univ Hosp, Dept Med Genet, Oslo, Norway
[7] Univ Queensland, Diamantina Inst, Translat Res Inst, Brisbane, Qld, Australia
[8] RMIT Univ, Funct Mat & Microsyst Res Grp & Micro Nano Res Fac, Melbourne, Australia
[9] Royal Brisbane Womens Hosp, Dept Otolaryngol, Brisbane, Qld, Australia
[10] Univ Queensland, Royal Brisbane & Womens Hosp, Sch Med, Brisbane, Qld, Australia
[11] Australian Translat Genom Ctr, Brisbane, Qld, Australia
[12] Griffith Univ, Menzies Hlth Inst Queensland MIHQ, Gold Coast, Qld, Australia
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Head and neck cancer; Circulating tumour DNA; Tumour DNA; DNA alterations; Biomarkers; Liquid biopsy; Precision medicine; EPSTEIN-BARR-VIRUS; HUMAN-PAPILLOMAVIRUS DNA; DROPLET DIGITAL PCR; HPV-NEGATIVE HEAD; CANCER-PATIENTS; PROMOTER HYPERMETHYLATION; MICROSATELLITE ANALYSIS; GENOMIC ALTERATIONS; COLORECTAL-CANCER; P53; ALTERATIONS;
D O I
10.1186/s12929-023-00953-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Head and Neck cancers (HNC) are a heterogeneous group of upper aero-digestive tract cancer and account for 931,922 new cases and 467,125 deaths worldwide. About 90% of these cancers are of squamous cell origin (HNSCC). HNSCC is associated with excessive tobacco and alcohol consumption and infection with oncogenic viruses. Genotyping tumour tissue to guide clinical decision-making is becoming common practice in modern oncology, but in the management of patients with HNSCC, cytopathology or histopathology of tumour tissue remains the mainstream for diagnosis and treatment planning. Due to tumour heterogeneity and the lack of access to tumour due to its anatomical location, alternative methods to evaluate tumour activities are urgently needed. Liquid biopsy approaches can overcome issues such as tumour heterogeneity, which is associated with the analysis of small tissue biopsy. In addition, liquid biopsy offers repeat biopsy sampling, even for patients with tumours with access limitations. Liquid biopsy refers to biomarkers found in body fluids, traditionally blood, that can be sampled to provide clinically valuable information on both the patient and their underlying malignancy. To date, the majority of liquid biopsy research has focused on blood-based biomarkers, such as circulating tumour DNA (ctDNA), circulating tumour cells (CTCs), and circulating microRNA. In this review, we will focus on ctDNA as a biomarker in HNSCC because of its robustness, its presence in many body fluids, adaptability to existing clinical laboratory-based technology platforms, and ease of collection and transportation. We will discuss mechanisms of ctDNA release into circulation, technological advances in the analysis of ctDNA, ctDNA as a biomarker in HNSCC management, and some of the challenges associated with translating ctDNA into clinical and future perspectives. ctDNA provides a minimally invasive method for HNSCC prognosis and disease surveillance and will pave the way in the future for personalized medicine, thereby significantly improving outcomes and reducing healthcare costs.
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页数:19
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