Long Noncoding RNA LINC00265 Targets EGFR and Promotes Deterioration of Colorectal Cancer: A Comprehensive Study Based on Data Mining and in vitro Validation
机构：[1]Department of Gastrointestinal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, People’s Republic of China[2]Quality Control Department, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, People’s Republic of China[3]Department of General Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing, People’s Republic of China临床科室普外科首都医科大学附属北京同仁医院首都医科大学附属同仁医院[4]Department of General Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People’s Republic of China
Background: LncRNAs are found to be aberrantly expressed in human cancers and could function as potential oncogenes or tumor suppressor genes. LINC00265 is a newly discovered LncRNA and its function in colorectal cancer (CRC) remains unknown. Methods: Comprehensive bioinformatics analysis were performed to investigate the expression, clinical significance and potential biologic functions of LINC00265 in CRC based on the data from the Cancer Genome Atlas (TCGA). To further investigate the potential role of LINC00265 in CRC, we knocked down the LINC00265 expression in HT29 cells. The cell proliferation, invasion, cycle distribution, and apoptosis were evaluated in control, NC and siRNA groups. Additionally, effect of LINC00265 on the expression of EGFR was also measured. Results: The expression level of LINC00265 is increased in CRC tissues. Elevated level of LINC00265 is correlated with lymph node metastases and advanced pathological stage. We obtained 269 LINC00265 related genes; the results of functional analysis of these genes revealed that LINC00265 might involve in carcinogenesis of CRC. In addition, further experiments indicated that LINC00265 knockdown impaired cell proliferation and invasion, promoted cell cycle distribution and apoptosis in HT29 cells. Moreover, Western blot analysis revealed that downregulation of LINC00265 suppressed the expression of EGFR. Conclusion: Our results indicate that LINC00265 induces cell proliferation, migration and inhibits CRC cells apoptosis by targeting EGFR. LINC00265 could be served as a diagnostic factor and therapeutic target for CRC patients.
基金：
Beijing Municipal
Administration of Hospital Clinical Medicine Development
of Special Funding Support (ZYLX201612).
第一作者机构：[1]Department of Gastrointestinal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, People’s Republic of China[*1]Department of Gastrointestinal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, No. 98 Fenghuang Road, Zunyi, Guizhou 563000, People’s Republic of China
通讯作者：
通讯机构：[1]Department of Gastrointestinal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, People’s Republic of China[*1]Department of Gastrointestinal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, No. 98 Fenghuang Road, Zunyi, Guizhou 563000, People’s Republic of China
推荐引用方式(GB/T 7714)：
Ge Hua,Yan Yan,Yue Chaosen,et al.Long Noncoding RNA LINC00265 Targets EGFR and Promotes Deterioration of Colorectal Cancer: A Comprehensive Study Based on Data Mining and in vitro Validation[J].ONCOTARGETS AND THERAPY.2019,12:10681-10692.doi:10.2147/OTT.S227482.
APA：
Ge, Hua,Yan, Yan,Yue, Chaosen,Liang, Chaojie&Wu, Jixiang.(2019).Long Noncoding RNA LINC00265 Targets EGFR and Promotes Deterioration of Colorectal Cancer: A Comprehensive Study Based on Data Mining and in vitro Validation.ONCOTARGETS AND THERAPY,12,
MLA：
Ge, Hua,et al."Long Noncoding RNA LINC00265 Targets EGFR and Promotes Deterioration of Colorectal Cancer: A Comprehensive Study Based on Data Mining and in vitro Validation".ONCOTARGETS AND THERAPY 12.(2019):10681-10692
