Composition and concentration of serum fatty acids of phospholipids depend on tumour location and disease progression in colorectal patients

• Main Authors: Bugajska Jolanta, Berska Joanna, Hodorowicz-Zaniewska Diana, Sztefko Krystyna
• Format: Article
• Language: English
• Published: Society of Medical Biochemists of Serbia, Belgrade 2018-01-01
• Series: Journal of Medical Biochemistry
• Subjects: polyunsaturated fatty acids; n-3 fatty acids; n-6 fatty acids; phospholipids; colorectal cancer
• Online Access: https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2018/1452-82581801039B.pdf
• ISSN: 1452-8258; 1452-8266

Background: Polyunsaturated fatty acids (PUFAs) play a role in the development/progression of colon cancer. The aim of the study was to assess the relation between serum phospholipids PUFAs, colorectal tumour localization and disease progression. Methods: A total of 67 patients (18 with proximal colon, 17 with distal colon and 32 with rectal tumour localization) as well as 16 controls were studied. One year after surgery, 33 patients had disease progression. Serum levels of C16:1(n-7), C18:1(n-9), C18:3(n-3), C20:5(n-3), C22:6(n3), C18:2(n-6), C20:2(n-6), C20:4(n-6) fatty acids of serum phospholipids were quantitatively measured before surgery by gas-chromatography. Results: Significantly higher mean value of C 18:2, as compared to control, has been noted only for patients with proximal (p< 0.05) and distal tumour (p< 0.03) localization. The lower mean level of C 20:5 and unsaturation index (UI) were observed in colorectal cancer patients regardless the tumour localization, but the statistical difference was noted only for patients with proximal tumours (p< 0.05, p<0.03). In patients with proximal tumours, significantly lower mean level of C 20:4 and UI were noted in patients with disease progression, as compared to patients with proximal tumours without disease progression (p< 0.05). Conclusions: The evaluation of PUFAs as a risk/prognostic factor in colorectal cancer patients should take into account tumour localization as a dependent variable.