Expression signature and prognostic value of CREC gene family in human colorectal cancer

被引:0
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作者
Junya Ning
Min Liu
Jing Shen
Deping Wang
Lijuan Gao
Huiyu Li
Jimin Cao
机构
[1] Shanxi Medical University,Key Laboratory of Cellular Physiology at Shanxi Medical University, Ministry of Education, and the Department of Physiology
[2] Shanxi Academy of Medical Sciences,Department of General Surgery, Shanxi Bethune Hospital
[3] Tongji Shanxi Hospital,Tongji Hospital, Tongji Medical College
[4] Third Hospital of Shanxi Medical University,undefined
[5] Huazhong University of Science and Technology,undefined
来源
BMC Cancer | / 23卷
关键词
CREC family; Expression signature; Colorectal cancer; Prognosis; Bioinformatics;
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摘要
Colorectal cancer (CRC) is one of the malignant tumors with the highest morbidity and mortality and poor prognosis. The mammalian gene family of Cab45/reticulocalbin/ERC-45/calumenin (CREC) consists of RCN1, RCN2, RCN3, SDF4 and CALU. Although CREC family members have been associated with CRC, the expression pattern, prognostic value, and the role of CREC family in CRC remain unclear. In this study, the expression, survival and biological functions of CREC family in CRC were determined via bioinformatic datasets analysis and experimental verification on clinical CRC specimen. Bioinformatic analysis showed that the expression levels of most CREC family genes were higher in CRC tissues than in normal colorectal tissues. The qPCR and western blot results also revealed that the transcriptional and protein levels of CREC family were elevated in CRC tissues compared with adjacent tissues. Besides, CREC family was significantly correlated with advanced tumor stage and poor prognosis of CRC patients. The expression levels of CREC family had correlations with genomic mutation and methylation, and with the infiltration levels of CD4 + T cells, macrophages, neutrophils, and dendritic cells in the microenvironment of CRC. Functional networks enrichment analysis indicated that the genes of CREC family were essential factors for CRC metastasis. Collectively, these findings suggest that CREC family might be potential targets for the treatment of CRC and candidate prognostic markers for CRC patients.
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