Suppressing TGFβ signaling in regenerating epithelia in an inflammatory microenvironment is sufficient to cause invasive intestinal cancer

• Published in: Cancer research (Chicago, Ill.) Vol. 75; no. 4; pp. 766 - 776
• Main Authors: Oshima, Hiroko, Nakayama, Mizuho, Han, Tae-Su, Naoi, Kuniko, Ju, Xiaoli, Maeda, Yusuke, Robine, Sylvie, Tsuchiya, Kiichiro, Sato, Toshiro, Sato, Hiroshi, Taketo, Makoto Mark, Oshima, Masanobu
• Format: Journal Article
• Language: English
• Published: United States 15.02.2015
• Subjects: Adenomatous Polyposis Coli Protein - genetics; Animals; Cell Proliferation - genetics; Colonic Neoplasms - genetics; Colonic Neoplasms - pathology; Female; Gene Expression Regulation, Neoplastic; Humans; Intestinal Mucosa - metabolism; Intestinal Mucosa - pathology; Intestinal Neoplasms - genetics; Matrix Metalloproteinase 2 - biosynthesis; Mice; Mice, Transgenic; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; Receptors, Transforming Growth Factor beta - genetics; Receptors, Transforming Growth Factor beta - metabolism; Signal Transduction; Transforming Growth Factor beta - genetics; Tumor Microenvironment
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/0008-5472.can-14-2036

Genetic alterations in the TGFβ signaling pathway in combination with oncogenic alterations lead to cancer development in the intestines. However, the mechanisms of TGFβ signaling suppression in malignant progression of intestinal tumors have not yet been fully understood. We have examined Apc(Δ716) Tgfbr2(ΔIEC) compound mutant mice that carry mutations in Apc and Tgfbr2 genes in the intestinal epithelial cells. We found inflammatory microenvironment only in the invasive intestinal adenocarcinomas but not in noninvasive benign polyps of the same mice. We thus treated simple Tgfbr2(ΔIEC) mice with dextran sodium sulfate (DSS) that causes ulcerative colitis. Importantly, these Tgfbr2(ΔIEC) mice developed invasive colon cancer associated with chronic inflammation. We also found that TGFβ signaling is suppressed in human colitis-associated colon cancer cells. In the mouse invasive tumors, macrophages infiltrated and expressed MT1-MMP, causing MMP2 activation. These results suggest that inflammatory microenvironment contributes to submucosal invasion of TGFβ signaling-repressed epithelial cells through activation of MMP2. We further found that regeneration was impaired in Tgfbr2(ΔIEC) mice for intestinal mucosa damaged by DSS treatment or X-ray irradiation, resulting in the expansion of undifferentiated epithelial cell population. Moreover, organoids of intestinal epithelial cells cultured from irradiated Tgfbr2(ΔIEC) mice formed "long crypts" in Matrigel, suggesting acquisition of an invasive phenotype into the extracellular matrix. These results, taken together, indicate that a simple genetic alteration in the TGFβ signaling pathway in the inflamed and regenerating intestinal mucosa can cause invasive intestinal tumors. Such a mechanism may play a role in the colon carcinogenesis associated with inflammatory bowel disease in humans.