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Fang. J Cancer Metastasis Treat 2020;6:1                            Journal of Cancer
               DOI: 10.20517/2394-4722.2019.42                           Metastasis and Treatment




               Editorial                                                                     Open Access


               Introduction to this Special Issue: “Biomarker
               Discovery and Precision Medicine”


               Bingliang Fang


               Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX 77030,
               USA.

               Correspondence to: Prof. Bingliang Fang, Department of Thoracic and Cardiovascular Surgery, The University of Texas MD
               Anderson Cancer Center, Houston, TX, USA. E-mail: bfang@mdanderson.org

               How to cite this article: Fang B. Introduction to this Special Issue: “Biomarker Discovery and Precision Medicine”. J Cancer
               Metastasis Treat 2020;6:1. http://dx.doi.org/10.20517/2394-4722.2019.42

               Received: 4 Dec 2019    Accepted: 5 Dec 2019    Published: 7 Jan 2020

               Science Editor: Judy S. Crabtree    Copy Editor: Jing-Wen Zhang    Production Editor: Tian Zhang




               With advances in genomics, transcriptomics, proteomics, and metabolomics, blooming data have been
               available for exploring molecular alternations in cancers. Many of these molecular alternations have been
               investigated as biomarkers for cancer diagnosis, prognosis, and precision therapies. It is my privilege to
               introduce this Special Issue of the Journal of Cancer Metastasis and Treatment, which contains four review
               articles and four original articles that focus on the topic of biomarker discoveries for cancer diagnosis and
               precision therapy.

               Solid tumors are known to shed their cellular components (proteins, nucleic acids, lipids, glycosaminoglycans,
               and metabolites) or malignant cells themselves into peripheral blood. Some of these molecules are already
                                                                            [1,2]
               used as biomarkers for cancer screenings and follow up tests in clinics . The advent of new technologies
               in genomics, proteomics, metabolomics, and cell biology analyses has dramatically expanded the scope
               of circulating tumor biomarkers from traditional tumor-associated antigens to circulating tumor cells,
               circulating tumor nucleic acids (cell free DNA and miRNA), exosomes, and plasma proteomics. The tests
                                                                                                        [3]
               on circulating tumor cells or tumor-specific nucleic acid in blood are also referred to as liquid biopsies .
               Three review articles in this Special Issue describe recent advances and challenges in liquid biopsy.
                       [4]
               Lai et al.  reviewed the use of membrane lipid-binding ligands in isolating subtypes of exosomes or
               extracellular vesicles for improvement of discovery and detection of disease-associated biomarkers in
                                          [5]
               peripheral blood. Huang et al.  discussed advances in developing new devices, such as microfluidics
               and nanotechnology, for capturing and molecular characterization of circulating tumor cells. Bookland


                           © The Author(s) 2020. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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