Prognostic significance of USP10 and p14ARF expression in patients with colorectal cancer

被引:18
作者
Kim, Kyungeun [1 ]
Huh, Tom [2 ]
Park, Yoonho [2 ]
Koo, Dong-Hoe [3 ]
Kim, Hungdai [4 ]
Hwang, Ilseon [5 ]
Choi, Chel Hun [6 ]
Yi, Joo Mi [7 ]
Chung, Joon-Yong [2 ]
机构
[1] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Dept Pathol, Sch Med, Seoul 03181, South Korea
[2] NCI, Expt Pathol Lab, Lab Pathol, Ctr Canc Res,NIH, MSC 1500, Bethesda, MD 20892 USA
[3] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Dept Internal Med, Div Hematol Oncol,Sch Med, Seoul 03181, South Korea
[4] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Dept Surg, Sch Med, Seoul 03181, South Korea
[5] Keimyung Univ, Dongsan Med Ctr, Dept Pathol, Sch Med, Daegu 42601, South Korea
[6] Sungkyunkwan Univ, Samsung Med Ctr, Dept Obstet & Gynecol, Sch Med, Seoul 06351, South Korea
[7] Inje Univ, Dept Microbiol & Immunol, Coll Med, Busan 47392, South Korea
基金
新加坡国家研究基金会;
关键词
USP10; p14ARF; methylation; prognosis; colorectal cancer; METHYLATION; BIOMARKER; HYPERMETHYLATION; DEUBIQUITINATION; STABILIZATION; INHIBITION; ACTIVATION; PROMOTER; GENES; P53;
D O I
10.1016/j.prp.2020.152988
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Ubiquitin-specific proteases (USPs) play an important role in fundamental cellular processes. Among these, USP10 is known for its association with tumor development and progression of multiple cancers. We aimed to investigate the clinical significance of USP10 expression in colorectal cancer and examined the potential link between USP10 and p14ARF in patients with colorectal cancer. USP10 and p14ARF protein expression was assessed via immunohistochemistry (IHC) on a tissue microarray from 280 colorectal cancer cases. IHC scores were evaluated by digital image analysis and compared with patients' outcomes. In addition, we examined DNA hypermethylation in colorectal cancer cell lines and tissues, which were matched with adjacent normal colon samples. USP10 expression was lost (USP10(loss)) in 18.6% of samples (52/280 cases), which was linked to lymphovascular invasion (p = 0.019) and distant metastases (p < 0.001). Similarly, loss of p14ARF expression (p14ARF(loss)) was associated with more advanced tumors. USP10 expression correlated positively with p14ARF expression (r = 0.617, p < 0.001). USP10(loss), p14ARF(loss), and dual loss of USP10 and p14ARF were significantly associated with shorter disease-free survival and overall survival in comparison to USP10(intact), p14ARF(intact), and dual loss of USP10 and p14ARF, respectively. Multivariate analysis revealed that USP10(loss) (p = 0.030) and dual loss of USP10 and p14ARF (p = 0.014) are independent prognostic factors for poor disease-free survival in colorectal cancer patients. Furthermore, aberrant hypermethylation of the USP10 promoter region was found in colorectal cancer cell lines and tissues. The present results suggest that USP10(loss) is a potential prognostic marker for colorectal cancer.
引用
收藏
页数:10
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