LMNB2 promotes the progression of colorectal cancer by silencing p21 expression

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作者
Chen-Hua Dong
Tao Jiang
Hang Yin
Hu Song
Yi Zhang
Hao Geng
Pei-Cong Shi
Yi-Xin Xu
Hong Gao
Lian-Yu Liu
Lei Zhou
Zhao-Hui Zhang
Jun Song
机构
[1] The Affiliated Hospital of Xuzhou Medical University,Department of General Surgery
[2] Xuzhou Medical University,The Graduate School
[3] Xuzhou Medical University,Institute of Digestive Diseases
[4] General Surgery,undefined
[5] 97th Hospital of Chinese People’s Liberation Army,undefined
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摘要
Colorectal cancer is the second common cause of death worldwide. Lamin B2 (LMNB2) is involved in chromatin remodeling and the rupture and reorganization of nuclear membrane during mitosis, which is necessary for eukaryotic cell proliferation. However, the role of LMNB2 in colorectal cancer (CRC) is poorly understood. This study explored the biological functions of LMNB2 in the progression of colorectal cancer and explored the possible molecular mechanisms. We found that LMNB2 was significantly upregulated in primary colorectal cancer tissues and cell lines, compared with paired non-cancerous tissues and normal colorectal epithelium. The high expression of LMNB2 in colorectal cancer tissues is significantly related to the clinicopathological characteristics of the patients and the shorter overall and disease-free cumulative survival. Functional analysis, including CCK8 cell proliferation test, EdU proliferation test, colony formation analysis, nude mouse xenograft, cell cycle, and apoptosis analysis showed that LMNB2 significantly promotes cell proliferation by promoting cell cycle progression in vivo and in vitro. In addition, gene set enrichment analysis, luciferase report analysis, and CHIP analysis showed that LMNB2 promotes cell proliferation by regulating the p21 promoter, whereas LMNB2 has no effect on cell apoptosis. In summary, these findings not only indicate that LMNB2 promotes the proliferation of colorectal cancer by regulating p21-mediated cell cycle progression, but also suggest the potential value of LMNB2 as a clinical prognostic marker and molecular therapy target.
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