| Literature DB >> 35158829 |
Marion Bacou1, Vidya Rajasekaran1, Adrian Thomson2, Sandra Sjöstrand3, Katarzyna Kaczmarek4, Anna Maria Ochocka-Fox5, Adam D Gerrard5, Susan Moug6, Tomas Jansson7,8, Helen Mulvana4, Carmel M Moran2, Susan M Farrington1.
Abstract
Lymph nodes (LNs) are believed to be the first organs targeted by colorectal cancer cells detached from a primary solid tumor because of their role in draining interstitial fluids. Better detection and assessment of these organs have the potential to help clinicians in stratification and designing optimal design of oncological treatments for each patient. Whilst highly valuable for the detection of primary tumors, CT and MRI remain limited for the characterization of LNs. B-mode ultrasound (US) and contrast-enhanced ultrasound (CEUS) can improve the detection of LNs and could provide critical complementary information to MRI and CT scans; however, the European Federation of Societies for Ultrasound in Medicine and Biology (EFSUMB) guidelines advise that further evidence is required before US or CEUS can be recommended for clinical use. Moreover, knowledge of the lymphatic system and LNs is relatively limited, especially in preclinical models. In this pilot study, we have created a mouse model of metastatic cancer and utilized 3D high-frequency ultrasound to assess the volume, shape, and absence of hilum, along with CEUS to assess the flow dynamics of tumor-free and tumor-bearing LNs in vivo. The aforementioned parameters were used to create a scoring system to predict the likelihood of a disease-involved LN before establishing post-mortem diagnosis with histopathology. Preliminary results suggest that a sum score of parameters may provide a more accurate diagnosis than the LN size, the single parameter currently used to predict the involvement of an LN in disease.Entities:
Keywords: 3D ultrasound; colorectal cancer; contrast-enhanced ultrasound; lymph node; metastatic mouse model; preclinical
Year: 2022 PMID: 35158829 PMCID: PMC8833694 DOI: 10.3390/cancers14030561
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639