| Literature DB >> 33535557 |
Alessandro Parisi1,2, Giampiero Porzio2,3, Fanny Pulcini3, Katia Cannita2,3, Corrado Ficorella2,3, Vincenzo Mattei4, Simona Delle Monache3.
Abstract
Despite the paradigmatic shift occurred in recent years for defined molecular subtypes in the metastatic setting treatment, colorectal cancer (CRC) still remains an incurable disease in most of the cases. Therefore, there is an urgent need for new tools and biomarkers for both early tumor diagnosis and to improve personalized treatment. Thus, liquid biopsy has emerged as a minimally invasive tool that is capable of detecting genomic alterations from primary or metastatic tumors, allowing the prognostic stratification of patients, the detection of the minimal residual disease after surgical or systemic treatments, the monitoring of therapeutic response, and the development of resistance, establishing an opportunity for early intervention before imaging detection or worsening of clinical symptoms. On the other hand, preclinical and clinical evidence demonstrated the role of gut microbiota dysbiosis in promoting inflammatory responses and cancer initiation. Altered gut microbiota is associated with resistance to chemo drugs and immune checkpoint inhibitors, whereas the use of microbe-targeted therapies including antibiotics, pre-probiotics, and fecal microbiota transplantation can restore response to anticancer drugs, promote immune response, and therefore support current treatment strategies in CRC. In this review, we aim to summarize preclinical and clinical evidence for the utilization of liquid biopsy and gut microbiota in CRC.Entities:
Keywords: CRC; CTC; ctDNA; gut microbiota; liquid biopsy; mi-RNA; nc-RNA
Year: 2021 PMID: 33535557 PMCID: PMC7912746 DOI: 10.3390/biomedicines9020140
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059