Ontology highlight
ABSTRACT: Background
Urothelial carcinoma (UC) is the fifth most common malignancy that accounts for 5% of all cancers. Diagnostic markers that predict UC progressions are inadequate. NF-?B contributes towards disease progression upon constitutive activation in many solid tumors. The nuclear localization of NF-?B indicates increased transcriptional activity while cytoplasmic localization indicates the inactive protein repository that can be utilized readily by a malignant cell. This study delineates the nuclear and cytoplasmic differential expression of NF-?B heterodimers in UC progression.Methods
The involvement of the NF-?B proteins in UC was analyzed in silico using cytoscape. The expression of NF-?B heterodimers was analyzed by immunohistochemistry.Results
PINA4MS app in cytoscape revealed over expression of RelA and suppression of NF-?B1 (p50 precursor) in UC whereas the expression of NF-?B target proteins remained unhindered. Immunohistochemical localization showed nuclear RelA/p50 in low grade UC whereas in high grade only RelA expression was observed. Conversely, cytoplasmic expression of RelA/p50 remained extensive across high and low grade UC tissues (p < 0.005). RelA nuclear and cytoplasmic expression (p < 0.005) was directly proportional to the disease progression. In our study, some of the high-grade UC tissues with squamous differentiation and muscle invasion had extensive nuclear p50 localization. The phenomenon of RelA/p50 expression seen increased in low-grade UC than high grade UC might be due to their interaction with other members of NF-?B family of proteins. Thus, NF-?B RelA/p50 differential expression may play a unique role in UC pathogenesis and can serve as a biomarker for diagnosis.
SUBMITTER: Durairajan S
PROVIDER: S-EPMC6139250 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature
PeerJ 20180913
<h4>Background</h4>Urothelial carcinoma (UC) is the fifth most common malignancy that accounts for 5% of all cancers. Diagnostic markers that predict UC progressions are inadequate. NF-κB contributes towards disease progression upon constitutive activation in many solid tumors. The nuclear localization of NF-κB indicates increased transcriptional activity while cytoplasmic localization indicates the inactive protein repository that can be utilized readily by a malignant cell. This study delineat ...[more]