HPLC of Formula: C10H12O3. Authors Roser, C; Toth, C; Renner, M; Herpel, E; Schirmacher, P in BMC published article about in [Roser, Christoph; Toth, Csaba; Renner, Marcus; Herpel, Esther; Schirmacher, Peter] Heidelberg Univ Hosp, Inst Pathol, Neuenheimer Feld 224, D-69120 Heidelberg, Germany; [Roser, Christoph] Heidelberg Univ Hosp, Dept Orthodont & Dentofacial Orthopaed, Neuenheimer Feld 400, D-69120 Heidelberg, Germany; [Herpel, Esther] Natl Ctr Tumor Dis NCT, Tissue Bank, Neuenheimer Feld 224, D-69120 Heidelberg, Germany; [Toth, Csaba] Trier MVZ Histol Cytol & Mol Diagnost, Max Planck Str 5, D-54296 Trier, Germany in 2021, Cited 53. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2
Background: Colorectal familial adenomatous polyposis (FAP) adenomas exhibit a uniform pathogenetic basis caused by a germline mutation in the adenomatous polyposis gene (APC), but the molecular changes leading to their development are incompletely understood. However, dysregulated apoptosis is known to substantially affect the development of colonic adenomas. One of the key regulatory proteins involved in apoptosis is apoptosis repressor with caspase recruitment domain (ARC). Methods: The expression of nuclear and cytoplasmic ARC in 212 adenomas from 80 patients was analyzed by immunohistochemistry. We also compared expression levels of ARC with the expression levels of p53, Bcl-2, COX-2, and MMR proteins. Statistical analyses were performed by Spearman’s rank correlation and linear regression test. Results: ARC was overexpressed in the nuclei and cytoplasm of most FAP adenomas investigated. Cytoplasmic ARC staining was moderately stronger (score 2) in 49.1% (n = 104/212) and substantially stronger (score 3) in 32.5% (n = 69/212) of adenomas compared to non-tumorous colorectal mucosa. In 18.4% (n = 39/212) of adenomas, cytoplasmic ARC staining was equivalent to that in non-tumorous mucosa. Nuclear expression of ARC in over 75% of cells was present in 30.7% (n = 65/212) of investigated adenomas, and nuclear expression in 10-75% of cells was detected in 62.7% (n = 133/212). ARC expression in under 10% of nuclei was found in 6.6% (n = 14/212) of adenomas. The correlation between nuclear ARC expression and cytoplasmic ARC expression was highly significant (p = 0.001). Moreover, nuclear ARC expression correlated positively with overexpression of Bcl-2, COX-2 p53 and beta-catenin. Cytoplasmic ARC also correlated with overexpression of Bcl-2. Sporadic MMR deficiency was detected in very few FAP adenomas and showed no correlation with nuclear or cytoplasmic ARC. Conclusions: Our results demonstrated that both cytoplasmic and nuclear ARC are overexpressed in FAP adenomas, thus in a homogenous collective. The highly significant correlation between nuclear ARC and nuclear beta-catenin suggested that ARC might be regulated by beta-catenin in FAP adenomas. Because of its further correlations with p53, Bcl-2, and COX-2, nuclear ARC might play a substantial role not only in carcinomas but also in precursor lesions.
HPLC of Formula: C10H12O3. Welcome to talk about 104-21-2, If you have any questions, you can contact Roser, C; Toth, C; Renner, M; Herpel, E; Schirmacher, P or send Email.
Reference:
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