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Cited by 412

The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.

The NOD-Like Receptor NLRP12 Attenuates Colon Inflammation and Tumorigenesis

Open access
Zaki, Md. Hasan, Vogel, Peter, Malireddi, R.K. Subbarao, Body-Malapel, Mathilde, Anand, Paras K., Bertin, John, Green, Douglas R., Lamkanfi, Mohamed, Kanneganti, Thirumala-Devi·2011·Cancer Cell

Abstract

SUMMARY NLRP12 is a member of the intracellular Nod-like receptor (NLR) family that has been suggested to down-regulate the production of inflammatory cytokines, but its physiological role in regulating inflammation has not been characterized. We generated mice deficient in Nlrp12 and studied its role in inflammatory diseases such as colitis and colorectal tumorigenesis. We show that Nlrp12-deficient mice are highly susceptible to colon inflammation and tumorigenesis, which is associated with increased production of inflammatory cytokines, chemokines and tumorigenic factors. Enhanced colon inflammation and colorectal tumor development in Nlrp12-deficient mice are due to a failure to dampen NF-κB and ERK activation in macrophages. These results reveal a critical role for NLRP12 in maintaining intestinal homeostasis and providing protection against colorectal tumorigenesis.

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Metadata

Authors
Zaki, M. H., Vogel, P., Malireddi, R. K. S., Body-Malapel, M., Anand, P. K., Bertin, J., Green, D. R., Lamkanfi, M., & Kanneganti, T.-D.
Venue
Cancer Cell
Publisher
Elsevier BV
Published
2011-11
Volume
20
Issue
5
Pages
649-660
ISSN
1535-6108 (ISSN-L)
OpenAlex
W2121722333
Cited by
412
References
10
FWCI
9.87
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: The NOD-Like Receptor NLRP12 Attenuates Colon Inflammation and Tumorigenesis. https://app.cochat.ai/papers/10.1016/j.ccr.2011.10.022
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Zaki, M. H., Vogel, P., Malireddi, R. K. S., Body-Malapel, M., Anand, P. K., Bertin, J., Green, D. R., Lamkanfi, M., & Kanneganti, T.-D. (2011). The NOD-Like Receptor NLRP12 Attenuates Colon Inflammation and Tumorigenesis. Cancer Cell. https://doi.org/10.1016/j.ccr.2011.10.022

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.