Tumor-Associated Macrophages Derived TGF-β‒Induced Epithelial to Mesenchymal Transition in Colorectal Cancer Cells through Smad2,3-4/Snail Signaling Pathway.
- Author:
Jianhui CAI
1
;
Limin XIA
;
Jinlei LI
;
Shichang NI
;
Huayu SONG
;
Xiangbin WU
Author Information
- Publication Type:Original Article
- Keywords: Tumor associated macrophages; Epithelial to mesenchymal transition; Transforming growth factor β; Colorectal neoplasms
- MeSH: Animals; Blotting, Western; Colorectal Neoplasms*; Cytokines; Eosine Yellowish-(YS); Flow Cytometry; Hematoxylin; Immunohistochemistry; Macrophages*; Neoplasm Metastasis; Real-Time Polymerase Chain Reaction; RNA, Messenger
- From:Cancer Research and Treatment 2019;51(1):252-266
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: We investigated the role of tumor-associated macrophages (TAMs) on the epithelial to mesenchymal transition (EMT) of colorectal cancer cells and determined the potential mechanism involved in the metastatic process. MATERIALS AND METHODS: In this study, flow cytometry was used to detect the expression of target proteins. We used transwell assay to evaluate the migration of cancer cells under specific conditions. Using real-time polymerase chain reaction, we examined the expressions of cytokines and EMT-related markers in mRNA level. Animal assay was performed for analysis in vivo and hematoxylin and eosin was used to visualize the effect of TAMs on tumor metastasis. We also used immunohistochemistry and Western blotting to detect the expression of target proteins. RESULTS: Here, we observed enrichment of TAMs in colorectal tumor tissues, resulting in high metastasis in clinical therapy. Moreover, those TAMs could facilitate the EMT progression of colorectal cancer cells, which is induced by the transforming growth factor-β (TGF-β) derived from TAMs, leading to the invasion and migration of cancer cells. CONCLUSION: Our results demonstrated that TAMs contributed the EMT progression through a TGF-β/Smad2,3-4/Snail signaling pathway, and disrupting this pathway with TGF-β receptor inhibitor could suppress metastasis, readjusting our focus to the connection of TAMs and cancer metastasis.
