3-nitrotyrosine and Carcinogenesis

3-nitrotyrosine has been researched along with Carcinogenesis* in 2 studies

Other Studies

2 other study(ies) available for 3-nitrotyrosine and Carcinogenesis

ArticleYear
Metformin inhibits the inflammatory and oxidative stress response induced by skin UVB-irradiation and provides 4-hydroxy-2-nonenal and nitrotyrosine formation and p53 protein activation.
    Journal of dermatological science, 2020, Volume: 100, Issue:2

    Topics: Aldehydes; Animals; Carcinogenesis; DNA Damage; Female; Humans; Melanoma; Metformin; Mice; Oxidative Stress; Radiation Injuries, Experimental; Radiodermatitis; Skin; Skin Neoplasms; Tumor Suppressor Protein p53; Tyrosine; Ultraviolet Rays

2020
Adenoma of colorectal laterally spreading tumor nongranular type with biological phenotypic features similar to cancer.
    Journal of gastroenterology and hepatology, 2018, Volume: 33, Issue:11

    Colorectal laterally spreading tumors (LSTs) are morphologically subdivided into granular (LST-G) and nongranular (LST-NG) categories. We aimed to elucidate the differences in oncogenic characteristics between the two types.. Laterally spreading tumors resected by endoscopic submucosal dissection and surgery from March 2009 to May 2017 were examined for p53 positivity, Ki-67 labeling index (LI), microvessel density, degree of fibrosis, intensities of inducible nitric oxide synthase (iNOS) and nitrotyrosine (NT), and expression of acid mucins. We compared these factors between adenomas, noninvasive cancers, and invasive cancers, both LST-G and LST-NG.. Ninety-three LST-G (53 adenomas [LST-GA] and 40 cancers [LST-GC]) and 55 LST-NG (24 adenomas [LST-NGA] and 31 cancers [LST-NGC]) were evaluated. Although p53 positivity was lower in LST-GA than in LST-NGA (P < 0.001), there was no difference between LST-GC and LST-NGC. Ki-67 LI was higher in LST-NGA than in LST-GA (P < 0.001) and higher in LST-NGC than in LST-GC of noninvasive cancers (P < 0.001). Microvessel density and degree of fibrosis were higher in LST-NGA than in LST-GA (P < 0.001), and intensities of iNOS and NT were also higher in LST-NGA than in LST-GA (P < 0.001). Expression of acid mucins was lower in LST-NGA than in LST-GA (P < 0.001). Although there were significant differences in p53 positivity, Ki-67 LI, microvessel density, degree of fibrosis, intensities of iNOS and NT, and expression of acid mucins between LST-GA and LST-NGA, these factors were only slightly different between LST-GC and LST-NGC of invasive cancers.. Unlike LST-GA, LST-NGA possessed phenotypic features similar to cancer.

    Topics: Adenoma; Carcinogenesis; Cohort Studies; Colorectal Neoplasms; Fibrosis; Humans; Intestinal Mucosa; Ki-67 Antigen; Microvessels; Mucins; Neoplasm Invasiveness; Nitric Oxide Synthase Type II; Phenotype; Retrospective Studies; Tumor Suppressor Protein p53; Tyrosine

2018