Inactivation of p21WAF1/cip1 enhances intestinal tumor formation in Muc2-/- mice

WanCai Yang, Anna Velcich, Ioana Lozonschi, Jiao Liang, Courtney Nicholas, Min Zhuang, Laura Bancroft, Leonard H. Augenlicht

Research output: Contribution to journalArticle

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Abstract

In the Apc1638+/- mouse model of intestinal tumorigenesis, targeted inactivation of the cyclin-dependent kinase inhibitor p21 WAF1/cip1 is highly effective in enhancing Apc-initiated tumor formation in the intestine. Because p21WAF1/cip1 plays a critical role in regulating intestinal cell proliferation, maturation, and tumorigenesis, we examined whether its inactivation would enhance tumor formation in a different mouse model of colon cancer. Therefore, we mated p21-/- mice with mice carrying a genetic deficiency of the Muc2 gene, which encodes the major gastrointestinal mucin. Muc2-/- mice develop tumors in the small and large intestine and the rectum, but in contrast to tumors in Apc1638+/- mice, this does not involve increased expression or nuclear localization of β-catenin. We found that inactivation of p21 WAF1/cip1 significantly increased the frequency and size of intestinal tumors in Muc2 knockout mice and also led to development of more invasive adenocarcinomas. This enhanced tumorigenesis significantly decreased mouse life span. Further, inactivation of p21WAF1/cip1 increased cell proliferation, decreased apoptosis, and decreased intestinal trefoil factor expression in the mucosa of both the small and large intestine. Surprisingly, reduced expression of p27kip1 was also observed in the Muc2 -/-, p21+/-, and p21-/- mice. In contrast, the expression of c-myc was significantly elevated. Thus, p21 modulates the formation of tumors whose initiation does (Apc) or does not (Muc2) involve altered β-catenin-Tcf4 signaling, but which may converge on common elements downstream of this signaling pathway.

Original languageEnglish (US)
Pages (from-to)1239-1246
Number of pages8
JournalAmerican Journal of Pathology
Volume166
Issue number4
StatePublished - Apr 2005

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Neoplasms
Catenins
Carcinogenesis
Large Intestine
Small Intestine
Cell Proliferation
Cyclin-Dependent Kinase Inhibitor p21
Mucins
Rectum
Knockout Mice
Colonic Neoplasms
Intestines
Mucous Membrane
Adenocarcinoma
Apoptosis
Genes

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Yang, W., Velcich, A., Lozonschi, I., Liang, J., Nicholas, C., Zhuang, M., ... Augenlicht, L. H. (2005). Inactivation of p21WAF1/cip1 enhances intestinal tumor formation in Muc2-/- mice. American Journal of Pathology, 166(4), 1239-1246.

Inactivation of p21WAF1/cip1 enhances intestinal tumor formation in Muc2-/- mice. / Yang, WanCai; Velcich, Anna; Lozonschi, Ioana; Liang, Jiao; Nicholas, Courtney; Zhuang, Min; Bancroft, Laura; Augenlicht, Leonard H.

In: American Journal of Pathology, Vol. 166, No. 4, 04.2005, p. 1239-1246.

Research output: Contribution to journalArticle

Yang, W, Velcich, A, Lozonschi, I, Liang, J, Nicholas, C, Zhuang, M, Bancroft, L & Augenlicht, LH 2005, 'Inactivation of p21WAF1/cip1 enhances intestinal tumor formation in Muc2-/- mice', American Journal of Pathology, vol. 166, no. 4, pp. 1239-1246.
Yang W, Velcich A, Lozonschi I, Liang J, Nicholas C, Zhuang M et al. Inactivation of p21WAF1/cip1 enhances intestinal tumor formation in Muc2-/- mice. American Journal of Pathology. 2005 Apr;166(4):1239-1246.
Yang, WanCai ; Velcich, Anna ; Lozonschi, Ioana ; Liang, Jiao ; Nicholas, Courtney ; Zhuang, Min ; Bancroft, Laura ; Augenlicht, Leonard H. / Inactivation of p21WAF1/cip1 enhances intestinal tumor formation in Muc2-/- mice. In: American Journal of Pathology. 2005 ; Vol. 166, No. 4. pp. 1239-1246.
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abstract = "In the Apc1638+/- mouse model of intestinal tumorigenesis, targeted inactivation of the cyclin-dependent kinase inhibitor p21 WAF1/cip1 is highly effective in enhancing Apc-initiated tumor formation in the intestine. Because p21WAF1/cip1 plays a critical role in regulating intestinal cell proliferation, maturation, and tumorigenesis, we examined whether its inactivation would enhance tumor formation in a different mouse model of colon cancer. Therefore, we mated p21-/- mice with mice carrying a genetic deficiency of the Muc2 gene, which encodes the major gastrointestinal mucin. Muc2-/- mice develop tumors in the small and large intestine and the rectum, but in contrast to tumors in Apc1638+/- mice, this does not involve increased expression or nuclear localization of β-catenin. We found that inactivation of p21 WAF1/cip1 significantly increased the frequency and size of intestinal tumors in Muc2 knockout mice and also led to development of more invasive adenocarcinomas. This enhanced tumorigenesis significantly decreased mouse life span. Further, inactivation of p21WAF1/cip1 increased cell proliferation, decreased apoptosis, and decreased intestinal trefoil factor expression in the mucosa of both the small and large intestine. Surprisingly, reduced expression of p27kip1 was also observed in the Muc2 -/-, p21+/-, and p21-/- mice. In contrast, the expression of c-myc was significantly elevated. Thus, p21 modulates the formation of tumors whose initiation does (Apc) or does not (Muc2) involve altered β-catenin-Tcf4 signaling, but which may converge on common elements downstream of this signaling pathway.",
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