| Literature DB >> 30554222 |
Takeshi Yamada1, Akihisa Matsuda2, Michihiro Koizumi2, Seiichi Shinji2, Goro Takahashi2, Takuma Iwai2, Kohki Takeda2, Kohji Ueda2, Yasuyuki Yokoyama2, Keisuke Hara2, Masahiro Hotta2, Satoshi Matsumoto2, Hiroshi Yoshida2.
Abstract
BACKGROUND: Liquid biopsy is a collective term that refers to the analysis of tumor-derived biomarkers isolated from biological fluids of cancer patients. Recently, many authors reported the usefulness of liquid biopsy for the management of malignancy. Summary and Key Messages: The peripheral blood of cancer patients is a pool of cells and/or cell products derived from the primary or metastatic tumor, including circulating tumor cells (CTCs), circulating free (cf) DNA or RNA, and exosomes containing proteins, nucleic acids, and lipids. CTCs are tumor cells that can be isolated from peripheral blood. Free circulating DNA with a tumor-specific mutation is called circulating tumor DNA (ctDNA). Some patients who undergo curative surgery experience recurrent disease, which can be due to the presence of minimal residual disease (MRD). Thus, MRD indicates a high risk of relapse. Detection of ctDNA or CTC after surgery is a direct proof of MRD. Molecular volume (e.g., the number of CTCs and level of ctDNA) might reflect tumor burden, thus high molecular volume may indicate poor prognosis. The most notable application of liquid biopsy in cancer is to understand spatial and temporal heterogeneities. Heterogeneity is one of the causes of refractoriness and hampers prediction of chemotherapeutic effect. Emerging mutations that are not present in primary tumors but are found in their metastases can be detected in ctDNA. Some colorectal cancer patients with wild-type RAS do not respond to epidermal growth factor receptor blockade. In a subset of these patients, RAS mutation is detected in ctDNA, indicating heterogeneity.Entities:
Keywords: Circulating tumor DNA; Circulating tumor cell; Heterogeneity; Minimal residual disease
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Year: 2018 PMID: 30554222 DOI: 10.1159/000494411
Source DB: PubMed Journal: Digestion ISSN: 0012-2823 Impact factor: 3.216