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Analysis of NF-κB and Clinical Prognostic Factors in Clear Cell Renal Cell Carcinoma
Korean Journal of Urological Oncology ; : 63-68, 2016.
Article in Korean | WPRIM | ID: wpr-23460
ABSTRACT

PURPOSE:

A multi-subunit transcription factor NF-κB is associated with anti-apoptotic signals in several cancers including renal cell carcinoma (RCC). In this study, we investigated whether the expression levels of the NF-κB were related to the clinical properties of human renal cell carcinoma such as nuclear grade, TNM stage, and recurrence free survival. MATERIALS AND

METHODS:

Patients who were diagnosed with clear cell RCC between January 2006 and February 2013 were included. Clinicopathological data and survival were investigated. The expressions of NF-κB were investigated by performing immunohistochemical staining on 61 clear cell RCC. The expression levels of NF-κB were divided two groups by the expression levels.

RESULTS:

Results on the expression of NF-κB were not significant. Analysis of NF-κB expressions is not associated with any of the clinical properties including age, nuclear grade and TNM stage (p=0.613, p=0.059, p=0.107, p=0.570, and p=0.760, respectively). Also, a statistically correlation was not observed between recurrence free survival and NF-κB expression levels (p=0.573).

CONCLUSIONS:

The expressions of the NF-κB were not associated with the clinical properties of clear cell RCC such as age, nuclear grade, TNM stage, and recurrence free survival.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Prognosis / Recurrence / Transcription Factors / Immunohistochemistry / Carcinoma, Renal Cell Type of study: Prognostic study Limits: Humans Language: Korean Journal: Korean Journal of Urological Oncology Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Prognosis / Recurrence / Transcription Factors / Immunohistochemistry / Carcinoma, Renal Cell Type of study: Prognostic study Limits: Humans Language: Korean Journal: Korean Journal of Urological Oncology Year: 2016 Type: Article