2022
DOI: 10.3390/jpm12060991
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TRIM24 Expression as an Independent Biomarker for Prognosis and Tumor Recurrence in HNSCC

Abstract: Background: Head and neck squamous cell carcinomas (HNSCCs) are among the most common cancers in humans worldwide and have a rather poor prognosis. TRIM24 has various intracellular functions and was identified in other cancer entities as a poor prognostic factor for patients. Methods: The expression of TRIM24 was evaluated by using immunohistochemistry. We used a large and representative cohort of 341 HNSCC patients. Data derived from immunohistochemistry evaluation was correlated with clinicopathological data… Show more

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Cited by 7 publications
(6 citation statements)
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“…The institutional ethic committee at the University Hospital Rostock approved the study (number A2022-0120), which was conducted in accordance with the Declaration of Helsinki of 1975. An independent, well-described cohort from primary HNSCCs was used as a control group to validate our prognostic findings [26][27][28].…”
Section: Patient Cohort and Multi Tumor Tissue Blocksmentioning
confidence: 99%
“…The institutional ethic committee at the University Hospital Rostock approved the study (number A2022-0120), which was conducted in accordance with the Declaration of Helsinki of 1975. An independent, well-described cohort from primary HNSCCs was used as a control group to validate our prognostic findings [26][27][28].…”
Section: Patient Cohort and Multi Tumor Tissue Blocksmentioning
confidence: 99%
“…SP140 might be a biomarker in head and neck squamous cell carcinoma ( 89 ). TRIM24 is a possible prognostic marker for prostate cancer ( 90 ), head and neck squamous cell carcinomas ( 91 ) and breast cancer ( 92 ). However, whether these indicators can be used as prognostic markers independently for OSC is still unclear.…”
Section: Discussionmentioning
confidence: 99%
“…We analyzed TRIM21 expression in HNSCC specimens derived from a cohort of 419 patients diagnosed between 2012 and 2015 at the Institute of Pathology of the University Medical Center Schleswig-Holstein, Germany, as reported previously [ 13 , 34 , 35 , 36 , 37 , 38 , 39 ]. Tumor samples were derived from PTs, LMs, RTs and DMs.…”
Section: Methodsmentioning
confidence: 99%
“…To assess the HPV status in the tumor samples, we used the p16 status as a surrogate marker [ 9 ]. Protein expression was detected with immunohistochemical staining using the mouse monoclonal antibody p16 (p16 CINtec ready to use kit, clone E6H4™, Roche Ventana Medical Systems, Tucson, AZ, USA), as described previously [ 18 , 38 ]. Binding was revealed using the Dab system delineated above.…”
Section: Methodsmentioning
confidence: 99%