Circulating PTGS2, JAG1, GUCY2C and PGF mRNA in Peripheral Blood and Serum as Potential Biomarkers for Patients with Metastatic Colon Cancer
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Jiménez Luna, Cristina; González Flores, Encarnación; Ortiz Quesada, Raúl; Martínez González, Luis Javier; Antúnez Rodríguez, Alba; Expósito Ruiz, Manuela; Melguizo Alonso, Consolación; Caba Pérez, Octavio; Prados Salazar, José CarlosEditorial
MDPI
Materia
Metastatic colon cancer Biomarkers Angiogenesis Liquid biopsies Circulating mRNA Digital PCR
Date
2021Referencia bibliográfica
Jimenez-Luna, C.; González-Flores, E.; Ortiz, R.; Martínez-González, L.J.; Antúnez-Rodríguez, A.; Expósito-Ruiz, M.; Melguizo, C.; Caba, O.; Prados, J. Circulating PTGS2, JAG1, GUCY2C and PGF mRNA in Peripheral Blood and Serum as Potential Biomarkers for Patients with Metastatic Colon Cancer. J. Clin. Med. 2021, 10, 2248. https://doi.org/10.3390/jcm10112248
Sponsorship
Instituto de Salud Carlos III (ISCIII) (Project PI19/01478) (FEDER) and by the CTS-107 GroupAbstract
Genes involved in the angiogenic process have been proposed for the diagnosis and
therapeutic response of metastatic colorectal cancer (CRC). This study aimed to investigate the value
of PTGS2, JAG1, GUCY2C and PGF-circulating RNA as biomarkers in metastatic CRC. Blood cells
and serum mRNA from 59 patients with metastatic CRC and 47 healthy controls were analyzed by
digital PCR. The area under the receiver operating characteristic curve (AUC) was used to estimate
the diagnostic value of each mRNA alone or mRNA combinations. A significant upregulation of the
JAG1, PTGS2 and GUCY2C genes in blood cells and serum samples from metastatic CRC patients
was detected. Circulating mRNA levels in the serum of all genes were significantly more abundant
than in blood. The highest discrimination ability between metastatic CRC patients and healthy
donors was obtained with PTGS2 (AUC of 0.984) and GUCY2C (AUC of 0.896) in serum samples.
Biomarker combinations did not improve the discriminatory capacity of biomarkers separately.
Analyzed biomarkers showed no correlation with overall survival or progression-free survival,
but GUCY2C and GUCY2C/PTGS2 expression in serum correlated significantly with the response
to antiangiogenic agents. These findings demonstrate that assessment of genes involved in the
angiogenic process may be a potential non-invasive diagnostic tool for metastatic CRC and its
response to antiangiogenic therapy.