Carcinoembryonic Antigen Interacts with TGF-β Receptor and Inhibits TGF-β Signaling in Colorectal Cancers

• Published in: Cancer research (Chicago, Ill.) Vol. 70; no. 20; pp. 8159 - 8168
• Main Authors: Li, Ying, Cao, Hong, Jiao, Zhongxian, Pakala, Suresh B., Sirigiri, Divijendra Natha Reddy, Li, Wenpin, Kumar, Rakesh, Mishra, Lopa
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 15.10.2010
• Subjects: Antineoplastic agents; Biological and medical sciences; Gastroenterology. Liver. Pancreas. Abdomen; Medical sciences; Pharmacology. Drug treatments; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors; Rectal disease; Tumor associated antigen; Oncofetal antigen; Transforming growth factor β; Colorectal cancer; Tumoral marker; Malignant tumor; Colonic disease; Carcinoembryonic antigen; Signal transduction; Digestive diseases; Intestinal disease; Inhibitor; Cancer; Biological receptor
• DOI: 10.1158/0008-5472.CAN-10-1073
• ISSN: 0008-5472

As a tumor marker for colorectal cancers, carcinoembryonic antigen (CEA) enhances the metastatic potential of cancer cells. CEA functions as an intercellular adhesion molecule and is upregulated in a wide variety of human cancers. However, the molecular mechanisms by which CEA mediates metastasis remain to be understood. Transforming growth factor-β (TGF-β) signaling regulates both tumor suppression and metastasis, and also contributes to the stimulation of CEA transcription and secretion in colorectal cancer cells. However, it remains unknown whether CEA, in turn, influences TGF-β functions and if a regulatory cross-talk exists between CEA and the TGF-β signaling pathway. Here, we report that CEA directly interacts with TGF-β receptor and inhibits TGF-β signaling. Targeting CEA with either CEA-specific antibody or siRNA rescues TGF-β response in colorectal cancer cell lines with elevated CEA, thereby restoring the inhibitory effects of TGF-β signaling on proliferation. CEA also enhances the survival of colorectal cancer cells in both local colonization and liver metastasis in animal study. Our study provides novel insights into the interaction between CEA and TGF-β signaling pathway and establishes a negative feedback loop in amplifying the progression of colon cancer cells to more invasive phenotypes. These findings offer new therapeutic opportunities to inhibit colorectal cancer cell proliferation by cotargeting CEA in promoting tumor-inhibitory action of the TGF-β pathway. Cancer Res; 70(20); 8159–68. ©2010 AACR.