Increased expression of Six1 correlates with progression and prognosis of prostate cancer
Autor: | Jun Zeng, Yan-Bin Song, Cuixia Cai, Rong Shi, Wen-Li Ma, Min Wei, Xin-rui Liu |
---|---|
Rok vydání: | 2015 |
Předmět: |
PCA3
Six1 Cancer Research Prostate cancer Tissue microarray business.industry Prognosis medicine.disease medicine.disease_cause Primary tumor medicine.anatomical_structure Oncology Prostate Tumor progression Genetics medicine Cancer research Biomarker (medicine) Primary Research business Carcinogenesis IHC |
Zdroj: | Cancer Cell International |
ISSN: | 1475-2867 |
DOI: | 10.1186/s12935-015-0215-z |
Popis: | Sineoculis homeobox homolog 1 (Six1), normally a developmentally restricted transcriptional regulator, is frequently dysregulated in mutiple cancers. Increasing evidences show that overexpression of Six1 plays a key role in tumorigenesis. However, the Six1 expression status and its relationship with the clinicopathological characteristics in prostate cancer were unclear. In this study, the mRNA and protein levels of Six1 in prostate cancer tissues and normal prostate tissues were evaluated. The clinicopathological significance of Six1 was investigated by immunohistochemistry (IHC) on a prostate cancer tissue microarray. The cut-off score for high expression of Six1 was determined by the receiver-operating characteristic (ROC) analysis. The correlation between Six1 protein expression and clinicopathological characteristics of prostate cancer was analyzed by Chi-square test. Increased expression of Six1 protein was observed in the majority of prostate cancer, compared with their paired adjacent normal prostate tissues. When Six1 high expression percentage was determined to be above 55 % (area under ROC curve = 0.881, P = 0.000), high expression of Six1 was observed in 55.6 % (80/144) of prostate cancer tissues and low expression of Six1 was observed in all normal prostate tissues by IHC. Increased expression of Six1 in patients was correlated with high histological grade (χ2 = 58.651, P = 0.00), advanced clinical stage (χ2 = 57.330, P = 0.000), high Gleason score (χ2 = 63.480, P = 0.000), high primary tumor grade (χ2 = 57.330, P = 0.000) and positive regional lymph node metastasis (χ2 = 19.294, P = 0.000). Furthermore, univariate and multivariate survival analysis suggested that Six1 was an independent prognostic indicator for overall survival (P |
Databáze: | OpenAIRE |
Externí odkaz: |