Abstract |
Colon cancer is the third most common malignancy and one of the leading causes of cancer-associated mortality worldwide. Neuronal pentraxin 1 (NPTX1) is associated with tumor progression in some types of tumors. However, its expression and role in colon cancer has not been yet reported. Here we observed that NPTX1 was down-regulated in colon cancer. Additionally, we explored the functional significance of NPTX1 in colon cancer. We found that over-expression of NPTX1 inhibited colon cancer cell growth by performing MTT, colony formation, Edu corporation assays, and cell cycle analysis. In vivo mouse experiments also confirmed the anti-proliferative role of NPTX1 in colon cancer. Further mechanistic study showed that over-expression of NPTX1 inhibited the expression of cyclin A2 and CDK2 in colon cancer cells, thereby regulating the Rb-E2F signaling. In summary, these findings reveal that NPTX1 suppress the colon cancer cell growth and might serve as a useful potential target for treatment of colon cancer.
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Authors | Xiaofeng Peng, Kangming Pan, Wenli Zhao, Jianzhu Zhang, Shicheng Yuan, Xiang Wen, Wenquan Zhou, Zhijin Yu |
Journal | Cell biology international
(Cell Biol Int)
Vol. 42
Issue 5
Pg. 589-597
(May 2018)
ISSN: 1095-8355 [Electronic] England |
PMID | 29345391
(Publication Type: Journal Article)
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Copyright | © 2018 International Federation for Cell Biology. |
Chemical References |
- CCNA2 protein, human
- Cyclin A2
- Nerve Tissue Proteins
- neuronal pentraxin
- C-Reactive Protein
- CDK2 protein, human
- Cyclin-Dependent Kinase 2
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Topics |
- Animals
- C-Reactive Protein
(metabolism, physiology)
- Cell Line, Tumor
- Cell Proliferation
- Colonic Neoplasms
(metabolism, pathology)
- Cyclin A2
(metabolism)
- Cyclin-Dependent Kinase 2
(metabolism)
- Down-Regulation
- Humans
- Mice
- Mice, Nude
- Nerve Tissue Proteins
(metabolism, physiology)
- Xenograft Model Antitumor Assays
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