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Cited by 1,085

The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.

PPARδ Is an APC-Regulated Target of Nonsteroidal Anti-Inflammatory Drugs

Open access
He, Tong-Chuan, Chan, Timothy A, Vogelstein, Bert, Kinzler, Kenneth W·1999·Cell

Abstract

PPARB was identified as a target of APC through the analysis of global gene expression profiles in human colorectal cancer (CRC) cells. PPARdelta expression was elevated in CRCs and repressed by APC in CRC cells. This repression was mediated by beta-catenin/Tcf-4-responsive elements in the PPARdelta promotor. The ability of PPARs to bind eicosanoids suggested that PPARdelta might be a target of chemopreventive non-steroidal anti-inflammatory drugs (NSAIDs). Reporters containing PPARdelta-responsive elements were repressed by the NSAID sulindac. Furthermore, sulindac was able to disrupt the ability of PPARdelta to bind its recognition sequences. These findings suggest that NSAIDs inhibit tumorigenesis through inhibition of PPARdelta, the gene for which is normally regulated by APC.

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Crossref · 10.1016/s0092-8674(00)81664-5

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Metadata

Authors
He, T.-C., Chan, T. A., Vogelstein, B., & Kinzler, K. W.
Venue
Cell
Publisher
Elsevier BV
Published
1999-10
Volume
99
Issue
3
Pages
335-345
ISSN
0092-8674 (ISSN-L)
OpenAlex
W1979201752
Cited by
1,085
References
55
FWCI
30.12
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: PPARδ Is an APC-Regulated Target of Nonsteroidal Anti-Inflammatory Drugs. https://app.cochat.ai/papers/10.1016/s0092-8674(00)81664-5
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He, T.-C., Chan, T. A., Vogelstein, B., & Kinzler, K. W. (1999). PPARδ Is an APC-Regulated Target of Nonsteroidal Anti-Inflammatory Drugs. Cell. https://doi.org/10.1016/s0092-8674(00)81664-5

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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.