Literature DB >> 25400738

CREPT expression correlates with poor prognosis in patients with retroperitoneal leiomyosarcoma.

Yaoguang She1, Jiao Liang2, Lin Chen2, Ying Qiu2, Na Liu1, Xudong Zhao1, Xiaohui Huang1, Yinyin Wang2, Fangli Ren2, Zhijie Chang2, Peiyu Li1.   

Abstract

Retroperitoneal leiomyosarcomas (LMSs) are rare gynecological malignancies that display poor prognosis and high mortality. Cell cycle-related and expression-elevated protein in tumor (CREPT) is an oncogene that is involved in the regulation of many cell cycle-related proteins. However, its distribution and clinical significance in retroperitoneal LMS remains poorly understood. This study assessed the histological classifications of postoperative tumor samples from 71 cases of retroperitoneal LMS that were collected at The General Hospital of the People's Liberation Army from January 1998 to December 2012. We found that more than half of the patients displayed positive expressions of CREPT, Ki-67 and PCNA via immunohistochemical analysis. The expression of CREPT correlated with histological grade (P = 0.044), and the PCNA expression level correlated with the differentiation of tumor cells and histological grade (P < 0.001 and P = 0.009, respectively). Multivariate analysis showed that survival was associated with histological grade and the expression level of CREPT (P = 0.011 and P = 0.012, respectively). Kaplan-Meier analysis showed that the patients lacking CREPT expression exhibited significantly longer overall postoperative survival (median, 60.0 months) than the patients displaying CREPT expression (median, 33.0 months), and CREPT expression correlated with distant recurrence within 5 years after surgery (P = 0.004). Western blot analyses showed that CREPT was more strongly expressed in the retroperitoneal LMS tumor tissue than in paired control tissue. Based on the above data, we concluded that CREPT displays unique immunostaining for retroperitoneal LMS tissue and can be used to supplement other currently available retroperitoneal LMS markers.

Entities:  

Keywords:  CREPT; leiomyosarcoma; prognosis; retroperitoneal neoplasms

Mesh:

Substances:

Year:  2014        PMID: 25400738      PMCID: PMC4230136     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  26 in total

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  12 in total

1.  An Important Role for RPRD1B in the Heat Shock Response.

Authors:  Simona Cugusi; Prashanth Kumar Bajpe; Richard Mitter; Harshil Patel; Aengus Stewart; Jesper Q Svejstrup
Journal:  Mol Cell Biol       Date:  2022-09-19       Impact factor: 5.069

2.  CREPT serves as a biomarker of poor survival in pancreatic ductal adenocarcinoma.

Authors:  Gang Yang; Yicheng Wang; Jianchun Xiao; Fangyu Zhao; Jiangdong Qiu; Yueze Liu; Guangyu Chen; Zhe Cao; Lei You; Lianfang Zheng; Taiping Zhang; Yupei Zhao
Journal:  Cell Oncol (Dordr)       Date:  2020-10-30       Impact factor: 6.730

3.  Inhibiting CREPT reduces the proliferation and migration of non-small cell lung cancer cells by down-regulating cell cycle related protein.

Authors:  Tao Liu; Wei-Miao Li; Wu-Ping Wang; Ying Sun; Yun-Feng Ni; Hao Xing; Jing-Hua Xia; Xue-Jiao Wang; Zhi-Pei Zhang; Xiao-Fei Li
Journal:  Am J Transl Res       Date:  2016-05-15       Impact factor: 4.060

4.  MicroRNA-383 acts as a tumor suppressor in colorectal cancer by modulating CREPT/RPRD1B expression.

Authors:  Jian Li; Amber R Smith; Rebecca T Marquez; Jun Li; Kun Li; Lan Lan; Xiaoqing Wu; Linxi Zhao; Fangli Ren; Yi Wang; Yinyin Wang; Baoqing Jia; Liang Xu; Zhijie Chang
Journal:  Mol Carcinog       Date:  2018-07-03       Impact factor: 4.784

Review 5.  Current understanding of CREPT and p15RS, carboxy-terminal domain (CTD)-interacting proteins, in human cancers.

Authors:  Mengdi Li; Danhui Ma; Zhijie Chang
Journal:  Oncogene       Date:  2020-11-25       Impact factor: 9.867

6.  Knocking-down of CREPT prohibits the progression of oral squamous cell carcinoma and suppresses cyclin D1 and c-Myc expression.

Authors:  Juntao Ma; Yipeng Ren; Lei Zhang; Xiangpan Kong; Tong Wang; Yueyi Shi; Rongfa Bu
Journal:  PLoS One       Date:  2017-04-03       Impact factor: 3.240

7.  CREPT facilitates colorectal cancer growth through inducing Wnt/β-catenin pathway by enhancing p300-mediated β-catenin acetylation.

Authors:  Yanquan Zhang; Shiyan Wang; Wei Kang; Chunxiao Liu; Yujuan Dong; Fangli Ren; Yinyin Wang; Jinglin Zhang; Guoping Wang; Ka Fai To; Xueji Zhang; Joseph Jy Sung; Zhijie Chang; Jun Yu
Journal:  Oncogene       Date:  2018-03-22       Impact factor: 9.867

8.  Overexpression of cell-cycle related and expression-elevated protein in tumor (CREPT) in malignant cervical cancer.

Authors:  Na Wen; Lihua Bian; Jing Gong; Yuanguang Meng
Journal:  J Int Med Res       Date:  2020-01       Impact factor: 1.671

9.  Overexpression of CREPT confers colorectal cancer sensitivity to fluorouracil.

Authors:  Yan-Shen Kuang; Yi Wang; Li-Dan Ding; Liu Yang; Ying Wang; Si-Han Liu; Bing-Tao Zhu; Xu-Ning Wang; Hong-Yi Liu; Jun Li; Zhi-Jie Chang; Yin-Yin Wang; Bao-Qing Jia
Journal:  World J Gastroenterol       Date:  2018-01-28       Impact factor: 5.742

10.  Cell cycle-related and expression-elevated protein in tumor overexpression is associated with proliferation behaviors and poor prognosis in non-small-cell lung cancer.

Authors:  Weimiao Li; Guoxu Zheng; Jinghua Xia; Guang Yang; Jianyong Sun; Xuejiao Wang; Miaomiao Wen; Ying Sun; Zhipei Zhang; Faguang Jin
Journal:  Cancer Sci       Date:  2018-03-05       Impact factor: 6.716

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