期刊
THERANOSTICS
卷 10, 期 5, 页码 2327-2341出版社
IVYSPRING INT PUBL
DOI: 10.7150/thno.39740
关键词
CCBE1; colorectal cancer; tumor lymphangiogenesis; lymphatic metastasis; TGF-beta
资金
- National Natural Science Foundation of China [81874177, 81672517, 31771545, 91749120, 81974060]
- Shanghai Committee of Science and Technology [16JC1404000]
- Program for Professor of Special Appointment (Young Eastern Scholar) at Shanghai Institutions of Higher Learning
- Shanghai Pujiang Program [18PJ1407400]
- Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant [20171918]
- Innovative research team of high-level local universities in Shanghai
Collagen and calcium-binding EGF domain-1 (CCBE1) is essential for lymphatic vascular development as it promotes vascular endothelial growth factor C (VEGFC) proteolysis. A recent study reported that CCBE1 was overexpressed in epithelial colorectal cancer (CRC) cells; however, the role of CCBE1 in tumor lymphangiogenesis and the mechanism underlying dysregulated CCBE1 expression in CRC remain undefined. Methods: The role of CCBE1 in tumor lymphangiogenesis and lymphatic metastasis was investigated using human lymphatic endothelial cells (HLECs) model in vitro, and a hindfoot lymphatic metastasis model in vivo. Immunochemistry analysis was performed to assess CCBE1 expression, prognostic value and correlation with clinicopathological characteristics in CRC. The biochemical function and transcriptional regulatory mechanism of CCBE1 were explored by western blot, qPCR, and chromatin immunoprecipitation. Results: Cancer cell-derived CCBE1 enhances VEGFC proteolysis in vitro, facilitates tube formation and migration of HLECs in vitro, and promotes tumor lymphangiogenesis and lymphatic metastasis in vivo. In addition to CRC cells, tumor stroma within CRC tissue shows high CCBE1 expression, which is associated with high lymphatic vessel density, increased lymph node metastasis and poor prognosis. Cancer-associated fibroblasts (CAFs) express and secret CCBE1, thereby contributing to VEGFC maturation and tumor lymphangiogenesis in CRC. Transforming growth factor beta (TGF-beta) downregulates the transcription and lymphangiogenic function of CCBE1 in CAFs and CRC cells through direct binding of SMADs to CCBE1 gene locus. Inactivation of the TGF-beta pathway correlates with increased CCBE1 expression in CRC. Conclusion: Our results demonstrate the protumorigenic role of CCBE1 in promoting lymphangiogenesis and lymphatic metastasis in CRC, revealing a new mechanism by which loss of TGF-beta signaling promotes CRC metastasis.
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