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Article

Plasma Uric Acid, Lactate, and Osmolality in Colorectal Cancer

1
Department of Biochemistry, Molecular Medicine and Nutrigenomics, Faculty of Pharmacy, Medical University “Prof. Dr. Paraskev Stoyanov”, 9002 Varna, Bulgaria
2
Department of General and Operative Surgery, Faculty of Medicine, Medical University “Prof. Dr. Paraskev Stoyanov”, 9002 Varna, Bulgaria
3
Department of Clinical Chemistry and Laboratory Diagnostics, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia in Katowice, 40-055 Katowice, Poland
4
Department of Community Pharmacy, Faculty of Pharmaceutical Sciences, Medical University of Silesia in Katowice, 40-055 Katowice, Poland
5
Department of Biology, Faculty of Pharmacy, Medical University “Prof. Dr. Paraskev Stoyanov”, 9002 Varna, Bulgaria
*
Author to whom correspondence should be addressed.
Appl. Sci. 2024, 14(13), 5630; https://doi.org/10.3390/app14135630
Submission received: 31 May 2024 / Revised: 20 June 2024 / Accepted: 22 June 2024 / Published: 27 June 2024
(This article belongs to the Section Applied Biosciences and Bioengineering)

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Plasma uric acid, lactate, and osmolality parameters can be used for screening and monitoring of colorectal cancer. Data about uric acid and lactate raise questions about the molecular mechanisms of their action in cancer development and the need for revisiting their importance, not only as metabolites but also as signaling molecules. The action of circulating plasma lactate may be different from those locally produced in tumor microenvironments.

Abstract

A complex evaluation of colorectal cancer (CRC) in relation to screening, diagnosis, stage determination, prognosis, and treatment requires valuable biomarkers. The aim of this study was to measure selected biomarkers––uric acid (UA), lactate, Na+, Cl−, and osmolality––in CRC patients and to assess their diagnostic value to distinguish between CRC and healthy controls. Plasma lactate (2.21 ± 0.11 vs. 2.88 ± 0.19, p < 0.01), Na+ (130.79 ± 0.42 vs. 133.23 ± 0.25, p < 0.001), Cl− (102.59 ± 0.45 vs. 103.94 ± 0.23, p < 0.01), and osmolality (266.44 ± 0.86 vs. 271.72 ± 0.62, p < 0.001) were found to be significantly lower in CRC patients as compared to the healthy controls group. Among them, with satisfactory diagnostic potential, were plasma Na+ concentrations and osmolality (AUCNa+ = 0.752, p < 0.0001; AUCosmolality = 0.757, p < 0.05), respectively. UA concentrations were detected at higher concentrations in CRC patients (333.67 ± 13.05 vs. 295.88 ± 13.78, p < 0.05). The results of this study contribute to the elucidation of molecular mechanisms of CRC pathogenesis and the role of studied metabolic parameters in this process. Plasma uric acid, lactate, and osmolality parameters can be used for screening and monitoring colorectal cancer. Further studies are required to elucidate the molecular mechanisms of their action in cancer development. The action of circulating plasma lactate may be different from those locally produced in the tumor microenvironment.
Keywords: colorectal cancer; uric acid; lactate; osmolality; hyponatremia colorectal cancer; uric acid; lactate; osmolality; hyponatremia

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MDPI and ACS Style

Kiselova-Kaneva, Y.; Vankova, D.; Kolev, N.; Kalinov, T.; Zlatarov, A.; Komosinska-Vassev, K.; Olczyk, P.; Yaneva, G.; Slavova, S.; Ivanov, K.; et al. Plasma Uric Acid, Lactate, and Osmolality in Colorectal Cancer. Appl. Sci. 2024, 14, 5630. https://doi.org/10.3390/app14135630

AMA Style

Kiselova-Kaneva Y, Vankova D, Kolev N, Kalinov T, Zlatarov A, Komosinska-Vassev K, Olczyk P, Yaneva G, Slavova S, Ivanov K, et al. Plasma Uric Acid, Lactate, and Osmolality in Colorectal Cancer. Applied Sciences. 2024; 14(13):5630. https://doi.org/10.3390/app14135630

Chicago/Turabian Style

Kiselova-Kaneva, Yoana, Deyana Vankova, Nikola Kolev, Turgay Kalinov, Alexandar Zlatarov, Katarzyna Komosinska-Vassev, Pawel Olczyk, Galina Yaneva, Svetla Slavova, Krasimir Ivanov, and et al. 2024. "Plasma Uric Acid, Lactate, and Osmolality in Colorectal Cancer" Applied Sciences 14, no. 13: 5630. https://doi.org/10.3390/app14135630

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