NOS2 Polymorphism in Aspect of Left and Right-Sided Colorectal Cancer
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NOS2 Polymorphism in Aspect of Left and Right-Sided Colorectal Cancer. / Klusek, Justyna; Lewitowicz, Piotr; Oblap, Ruslan; Orlewska, Ewa; Witczak, Bartosz; Marzec, Michał Tomasz; Kozłowska-Geller, Monika; Nawacki, Łukasz; Wawszczak-Kasza, Monika; Kocańda, Kamila; Jóźwik, Artur; Głuszek, Stanisław.
In: Journal of Clinical Medicine, Vol. 13, No. 4, 937, 2024.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - NOS2 Polymorphism in Aspect of Left and Right-Sided Colorectal Cancer
AU - Klusek, Justyna
AU - Lewitowicz, Piotr
AU - Oblap, Ruslan
AU - Orlewska, Ewa
AU - Witczak, Bartosz
AU - Marzec, Michał Tomasz
AU - Kozłowska-Geller, Monika
AU - Nawacki, Łukasz
AU - Wawszczak-Kasza, Monika
AU - Kocańda, Kamila
AU - Jóźwik, Artur
AU - Głuszek, Stanisław
PY - 2024
Y1 - 2024
N2 - Background: The NOS2 gene polymorphism rs2297518 is associated with an increased level of NO, which could contribute to colorectal cancer (CRC) development. We hypothesized that the potential influence of the NOS2 gene polymorphism on cancer development may vary between right-sided and left-sided colon cancers, and rectal cancers. The aim of this study was to determine the rs2297518 polymorphism influence on colorectal cancer development with regard to tumor localization. Methods: This case–control study included 199 patients with CRC and 120 controls. The qPCR endpoint genotyping was conducted using the TaqMan® genotyping assay. Results: This study revealed significant differences in tumor characteristic and in the minor alelle A frequency in the NOS2 genotype between colorectal cancers with different localizations. The mucinous adenocarcinoma was diagnosed significantly more often in right-sided cancers than in left-sided (30.6% vs. 10.9%, p = 0.009) and rectal cancers (30.6% vs. 7.1%, p = 0.0003). The minor allele A of the NOS2 genotype was observed more frequently in right-sided cancers than in left-sided cancers (44.9% vs. 23.1%, p = 0.0137) and more frequently in rectal cancers than in left-sided cancers (40.0% vs. 23.1%, p = 0.0285). Conclusions: In conclusion, the results support the hypothesis that the SNP rs2297518 of the NOS2 gene influences colorectal cancer development with regard to tumor localization.
AB - Background: The NOS2 gene polymorphism rs2297518 is associated with an increased level of NO, which could contribute to colorectal cancer (CRC) development. We hypothesized that the potential influence of the NOS2 gene polymorphism on cancer development may vary between right-sided and left-sided colon cancers, and rectal cancers. The aim of this study was to determine the rs2297518 polymorphism influence on colorectal cancer development with regard to tumor localization. Methods: This case–control study included 199 patients with CRC and 120 controls. The qPCR endpoint genotyping was conducted using the TaqMan® genotyping assay. Results: This study revealed significant differences in tumor characteristic and in the minor alelle A frequency in the NOS2 genotype between colorectal cancers with different localizations. The mucinous adenocarcinoma was diagnosed significantly more often in right-sided cancers than in left-sided (30.6% vs. 10.9%, p = 0.009) and rectal cancers (30.6% vs. 7.1%, p = 0.0003). The minor allele A of the NOS2 genotype was observed more frequently in right-sided cancers than in left-sided cancers (44.9% vs. 23.1%, p = 0.0137) and more frequently in rectal cancers than in left-sided cancers (40.0% vs. 23.1%, p = 0.0285). Conclusions: In conclusion, the results support the hypothesis that the SNP rs2297518 of the NOS2 gene influences colorectal cancer development with regard to tumor localization.
KW - colorectal cancer
KW - gene polymorphism right-sided CRC
KW - left-sided CRC
KW - NOS2
U2 - 10.3390/jcm13040937
DO - 10.3390/jcm13040937
M3 - Journal article
C2 - 38398251
AN - SCOPUS:85185964391
VL - 13
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
SN - 2077-0383
IS - 4
M1 - 937
ER -
ID: 385140553