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.

Highlights

  • Gli1 expression seems to be involved in the process of epithelial–mesenchymal transition (EMT), which is a necessary step in promoting invasion and metastasis in colorectal cancer (CRC) [51]

  • As demonstrated by Hefazi et al in cancer patients treated with cytotoxic chemotherapy, fecal microbiota transplantation (FMT) treatment determined a reduction of multiply recurrent Clostridium difficile infection (CDI) and diarrhea episodes remarking its highly therapeutic efficacy [135]

  • The lack of clinical applicability is currently due to the large quantity of liquid biopsy assays, with different detection limits, sensitivity, and specificity [138]

Read more

Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Primary tumor resection is eventually associated to adjuvant chemotherapy with fluoropyrimidines with or without oxaliplatin according to TNM stage and pathological risk factors in early CRC [3], does not always seem sufficient to eliminate circulating tumor cells (CTCs) and other components involved in establishing pre-metastatic niche-promoting immune evasion and maintenance of stemness [4]. Biomedicines 2021, 9, 140 pathological risk factors in early CRC [3], does not always seem sufficient to eliminate circulating tumor cells (CTCs) and other components involved in establishing pre-metastatic niche-promoting immune evasion and maintenance of stemness [4]. 1. Potential cells (CTCs), circulating tumor DNA (ctDNA), non-coding RNA (ncRNA), and exosomes are promising liquid biopsy markers for colorectal cancer with multiple potential advantages compared to tissue biopsy.

Liquid Biopsy
Screening and Early Diagnosis
CRC based on ctDNA
A Phase II Clinical Trial
Diagnosis and Prognosis
Drug Resistance
Microbiota
Microbiota and Cancer
Signaling Pathways Activated in Microbiota and Cancer
Microbiota and Efficacy of Anticancer Agents
Recent Advances in Metagenomics Technology for Diagnosis and Prognosis
Organoids Engineering
Future Perspectives and Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call