TY - JOUR
T1 - c-Jun NH2-terminal kinase 1 plays a critical role in intestinal homeostasis and tumor suppression
AU - Tong, Chang
AU - Yin, Zhinan
AU - Song, Zibo
AU - Dockendorff, Ashley
AU - Huang, Chuanshu
AU - Mariadason, John
AU - Flavell, Richard A.
AU - Davis, Roger J.
AU - Augenlicht, Leonard H.
AU - Yang, Wancai
N1 - Funding Information:
Supported in part by the National Cancer Institute (grants R01 CA112081 to W.Y., U54 CA100926 to L.H.A., and P30-13330 (to the Albert Einstein Cancer Center) and the American Institute for Cancer Research (grant 05A121 to W.Y.).
PY - 2007/7
Y1 - 2007/7
N2 - The c-Jun NH2-terminal kinase (JNK) signal transduction pathway plays important roles in cellular processes and stress. However, the role of JNK1 in intestinal homeostasis and tumorigenesis is unknown. Therefore, we used a JNK1 knockout mouse model to characterize intestinal cell maturation and tumorigenesis. In addition, colon cancer cell lines were used to validate the role of JNK1 and to elucidate the underlying molecular mechanisms in vitro. To our surprise, we found that mice with targeted inactivation of JNK1 spontaneously developed intestinal tumors. The normal mucosa in JNK1-deficient mice showed decreased cell differentiation and increased cell proliferation. This tumorigenesis was closely linked to the down-regulation of p21 WAF1/cip1, a cyclln-dependent kinase inhibitor, in intestinal epithelial cells. Immunohistochemical staining showed that JNK1 was highly expressed in the differentiation compartment of the intestinal mucosa and that the expression of JNK1 was significantly decreased in both human colonic and mouse intestinal tumors. In the colon cancer cell lines, JNK1 expression was up-regulated during spontaneous differentiation, corresponding to the up-regulation of p21WAF1/cip1. Moreover, butyrateinduced p21 expression was linked to phosphorylation of JNK1. Reduced JNK1 expression by small interfering RNA suppressed butyrate-induced apoptosis. We concluded that JNK1 plays a critical role in the regulation of homeostasis and in the suppression of tumor formation in the intestine, which was linked to the altered expression of p21WAF1/cip1.
AB - The c-Jun NH2-terminal kinase (JNK) signal transduction pathway plays important roles in cellular processes and stress. However, the role of JNK1 in intestinal homeostasis and tumorigenesis is unknown. Therefore, we used a JNK1 knockout mouse model to characterize intestinal cell maturation and tumorigenesis. In addition, colon cancer cell lines were used to validate the role of JNK1 and to elucidate the underlying molecular mechanisms in vitro. To our surprise, we found that mice with targeted inactivation of JNK1 spontaneously developed intestinal tumors. The normal mucosa in JNK1-deficient mice showed decreased cell differentiation and increased cell proliferation. This tumorigenesis was closely linked to the down-regulation of p21 WAF1/cip1, a cyclln-dependent kinase inhibitor, in intestinal epithelial cells. Immunohistochemical staining showed that JNK1 was highly expressed in the differentiation compartment of the intestinal mucosa and that the expression of JNK1 was significantly decreased in both human colonic and mouse intestinal tumors. In the colon cancer cell lines, JNK1 expression was up-regulated during spontaneous differentiation, corresponding to the up-regulation of p21WAF1/cip1. Moreover, butyrateinduced p21 expression was linked to phosphorylation of JNK1. Reduced JNK1 expression by small interfering RNA suppressed butyrate-induced apoptosis. We concluded that JNK1 plays a critical role in the regulation of homeostasis and in the suppression of tumor formation in the intestine, which was linked to the altered expression of p21WAF1/cip1.
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U2 - 10.2353/ajpath.2007.061036
DO - 10.2353/ajpath.2007.061036
M3 - Article
C2 - 17591974
AN - SCOPUS:34547653108
SN - 0002-9440
VL - 171
SP - 297
EP - 303
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 1
ER -