Guan Bo, Ran Xian-Gui, Du Yong-Qiang, Ren Feng, Tian Ye, Wang Ying, Chen Ming-Min
Department of Urology, Capital Medical University, Beijing Friendship Hospital Beijing, P. R. China.
Department of Urology, Fuyang People's Hospital Yingzhou District, Fuyang, Anhui Province, P. R. China.
Int J Clin Exp Pathol. 2018 Jul 1;11(7):3697-3702. eCollection 2018.
Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal cell carcinoma. The chromo-helicase-DNA binding proteins (CHDs), containing nine members named CHD1-9, act as regulators of the chromatin remodeling process and gene expression. To determine the correlation between CHD9 expression and ccRCC, we performed an immunohistochemical staining in a tissue microarray (TMAs) containing tissue samples from 88 ccRCC patients. The results showed that cytoplasm CHD9 expression was statistically decreased in tumor tissues compared to adjacent tissues (8.54±2.90 vs 12.61±2.05, =0.000), while nuclear CHD9 expression was upregulated in the tumor tissues (1.47±2.93 vs 0.29±1.24, =0.000). A univariate analysis found that cytoplasm CHD9 expression in cancer tissues was correlated with the patients' pathological grading (=0.002, r=0.330), the clinical stages (=0.02, r=0.250) and the T grading (=0.024, r=0.241) significantly. In addition, cytoplasm CHD9 expression in non-tumor tissues was correlated with the ccRCC patients' pathological grading (=0.031, r=-0.231) significantly. Patients with high cytoplasm CHD9 expression had a significantly worse prognosis than those with low cytoplasm CHD9 expression levels (59.7% vs 85.7%, =0. 042). In conclusion, our study indicated the important role of CHD9 in ccRCC and suggested CHD9 may be a potential biomarker for prognostic prediction and a new target for therapy.
透明细胞肾细胞癌(ccRCC)是肾细胞癌最常见的亚型。包含CHD1 - 9九个成员的染色体解旋酶 - DNA结合蛋白(CHDs),作为染色质重塑过程和基因表达的调节因子。为了确定CHD9表达与ccRCC之间的相关性,我们在一个包含88例ccRCC患者组织样本的组织微阵列(TMAs)中进行了免疫组织化学染色。结果显示,与相邻组织相比,肿瘤组织中细胞质CHD9表达在统计学上显著降低(8.54±2.90对12.61±2.05,P = 0.000),而肿瘤组织中细胞核CHD9表达上调(1.47±2.93对0.29±1.24,P = 0.000)。单因素分析发现,癌组织中细胞质CHD9表达与患者的病理分级(P = 0.002,r = 0.330)、临床分期(P = 0.02,r = 0.250)和T分级(P = 0.024,r = 0.241)显著相关。此外,非肿瘤组织中细胞质CHD9表达与ccRCC患者的病理分级(P = 0.031,r = -0.231)显著相关。细胞质CHD9高表达的患者预后明显比细胞质CHD9低表达水平的患者差(59.7%对85.7%,P = 0.042)。总之,我们的研究表明CHD9在ccRCC中具有重要作用,并提示CHD9可能是预后预测的潜在生物标志物和新的治疗靶点。