Blood-based liquid biopsy: Insights into early detection and clinical management of lung cancer.


Journal

Cancer letters
ISSN: 1872-7980
Titre abrégé: Cancer Lett
Pays: Ireland
ID NLM: 7600053

Informations de publication

Date de publication:
01 01 2022
Historique:
received: 30 07 2021
revised: 22 09 2021
accepted: 11 10 2021
pubmed: 18 10 2021
medline: 8 1 2022
entrez: 17 10 2021
Statut: ppublish

Résumé

Currently, early detection of lung cancer relies on the characterisation of images generated from computed tomography (CT). However, lung tissue biopsy, a highly invasive surgical procedure, is required to confirm CT-derived diagnostic results with very high false-positive rates. Hence, a non-invasive or minimally invasive biomarkers is essential to complement the existing low-dose CT (LDCT) for early detection, improve responses to a certain treatment, predict cancer recurrence, and to evaluate prognosis. In the past decade, liquid biopsies (e.g., blood) have been demonstrated to be highly effective for lung cancer biomarker discovery. In this review, the roles of emerging liquid biopsy-derived biomarkers such as circulating nucleic acids, circulating tumour cells (CTCs), long non-coding RNA (lncRNA), and microRNA (miRNA), as well as exosomes, have been highlighted. The advantages and limitations of these blood-based minimally invasive biomarkers have been discussed. Furthermore, the current progress of the identified biomarkers for clinical management of lung cancer has been summarised. Finally, a potential strategy for the early detection of lung cancer, using a combination of LDCT scans and well-validated biomarkers, has been discussed.

Identifiants

pubmed: 34656690
pii: S0304-3835(21)00523-1
doi: 10.1016/j.canlet.2021.10.013
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
MicroRNAs 0
RNA, Long Noncoding 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

91-102

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Cuiliu Liu (C)

School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China.

Xiaoqiang Xiang (X)

Department of Clinical Pharmacy and Pharmacy Administration, School of Pharmacy, Fudan University, Shanghai, 201203, China.

Shuangqing Han (S)

School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China.

Hannah Ying Lim (HY)

Department of Pharmacy, Faculty of Science, National University of Singapore, 117543, Singapore.

Lingrui Li (L)

School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China.

Xing Zhang (X)

School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China.

Zhaowu Ma (Z)

School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China.

Li Yang (L)

The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Shuliang Guo (S)

The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Ross Soo (R)

Department of Haematology-Oncology, National University Cancer Institute, 119228, Singapore.

Boxu Ren (B)

School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China. Electronic address: boxuren188@163.com.

Lingzhi Wang (L)

Cancer Science Institute of Singapore, National University of Singapore, 117599, Singapore; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, 117600, Singapore. Electronic address: csiwl@nus.edu.sg.

Boon Cher Goh (BC)

Department of Haematology-Oncology, National University Cancer Institute, 119228, Singapore; Cancer Science Institute of Singapore, National University of Singapore, 117599, Singapore; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, 117600, Singapore.

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Classifications MeSH