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Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.评估患有 CHD7 变异的先天性低促性腺激素性性腺功能减退症患者中的 CHARGE 综合征。
Genet Med. 2018 Aug;20(8):872-881. doi: 10.1038/gim.2017.197. Epub 2017 Nov 16.
2
miR-93-3p inhibition suppresses clear cell renal cell carcinoma proliferation, metastasis and invasion.miR-93-3p抑制可抑制肾透明细胞癌的增殖、转移和侵袭。
Oncotarget. 2017 Aug 24;8(47):82824-82834. doi: 10.18632/oncotarget.20458. eCollection 2017 Oct 10.
3
NUDT expression is predictive of prognosis in patients with clear cell renal cell carcinoma.NUDT表达可预测透明细胞肾细胞癌患者的预后。
Oncol Lett. 2017 Nov;14(5):6121-6128. doi: 10.3892/ol.2017.6997. Epub 2017 Sep 18.
4
Localization of TFPI-2 in the nucleus modulates MMP-2 gene expression in breast cancer cells.TFPI-2 在核内的定位调节乳腺癌细胞中 MMP-2 基因的表达。
Sci Rep. 2017 Oct 19;7(1):13575. doi: 10.1038/s41598-017-14148-8.
5
RNAi screens identify CHD4 as an essential gene in breast cancer growth.RNA干扰筛选确定CHD4是乳腺癌生长中的一个必需基因。
Oncotarget. 2016 Dec 6;7(49):80901-80915. doi: 10.18632/oncotarget.12646.
6
Loss of CHD1 causes DNA repair defects and enhances prostate cancer therapeutic responsiveness.CHD1的缺失会导致DNA修复缺陷并增强前列腺癌的治疗反应性。
EMBO Rep. 2016 Nov;17(11):1609-1623. doi: 10.15252/embr.201642352. Epub 2016 Sep 5.
7
Nuclear localization of Toll-like receptor 5 in Barrett's esophagus and esophageal adenocarcinoma is associated with metastatic behavior.Toll样受体5在巴雷特食管和食管腺癌中的核定位与转移行为相关。
Virchows Arch. 2016 Oct;469(4):465-70. doi: 10.1007/s00428-016-1989-7. Epub 2016 Jul 9.
8
Chromodomain-helicase-DNA binding protein 5, 7 and pronecrotic mixed lineage kinase domain-like protein serve as potential prognostic biomarkers in patients with resected pancreatic adenocarcinomas.染色质结构域解旋酶DNA结合蛋白5、7和促坏死混合谱系激酶样蛋白可作为切除性胰腺腺癌患者潜在的预后生物标志物。
World J Gastrointest Oncol. 2016 Apr 15;8(4):358-65. doi: 10.4251/wjgo.v8.i4.358.
9
Molecular characterization of clear cell renal cell carcinoma identifies CSNK2A1, SPP1 and DEFB1 as promising novel prognostic markers.透明细胞肾细胞癌的分子特征鉴定出CSNK2A1、SPP1和DEFB1为有前景的新型预后标志物。
APMIS. 2016 May;124(5):372-83. doi: 10.1111/apm.12519. Epub 2016 Feb 15.
10
New Face for Chromatin-Related Mesenchymal Modulator: n-CHD9 Localizes to Nucleoli and Interacts With Ribosomal Genes.染色质相关间充质调节剂的新面孔:n-CHD9定位于核仁并与核糖体基因相互作用。
J Cell Physiol. 2015 Sep;230(9):2270-80. doi: 10.1002/jcp.24960.

高CHD9表达与透明细胞肾细胞癌的不良预后相关。

High CHD9 expression is associated with poor prognosis in clear cell renal cell carcinoma.

作者信息

Guan Bo, Ran Xian-Gui, Du Yong-Qiang, Ren Feng, Tian Ye, Wang Ying, Chen Ming-Min

机构信息

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.

出版信息

Int J Clin Exp Pathol. 2018 Jul 1;11(7):3697-3702. eCollection 2018.

PMID:31949752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6962849/
Abstract

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.

摘要

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。