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Cited by 287

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Curcumin inhibits cyclooxygenase-2 transcription in bile acid- and phorbol ester-treated human gastrointestinal epithelial cells

Open access
Zhang, Fan, Altorki, Nasser K., Mestre, Juan R., Subbaramaiah, Kotha, Dannenberg, Andrew J.·1999·Carcinogenesis

Abstract

We investigated whether curcumin, a chemopreventive agent, inhibited chenodeoxycholate (CD)- or phorbol ester (PMA)-mediated induction of cyclooxygenase-2 (COX-2) in several gastrointestinal cell lines (SK-GT-4, SCC450, IEC-18 and HCA-7). Treatment with curcumin suppressed CD- and PMA-mediated induction of COX-2 protein and synthesis of prostaglandin E2. Curcumin also suppressed the induction of COX-2 mRNA by CD and PMA. Nuclear run-offs revealed increased rates of COX-2 transcription after treatment with CD or PMA and these effects were inhibited by curcumin. Treatment with CD or PMA increased binding of AP-1 to DNA. This effect was also blocked by curcumin. In addition to the above effects on gene expression, we found that curcumin directly inhibited the activity of COX-2. These data provide new insights into the anticancer properties of curcumin.

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Metadata

Authors
Zhang, F., Altorki, N. K., Mestre, J. R., Subbaramaiah, K., & Dannenberg, A. J.
Venue
Carcinogenesis
Published
1999-03
Volume
20
Issue
3
Pages
445-451
ISSN
  • 0143-3334 (ISSN-L)
  • 1460-2180
OpenAlex
W2141909270
Cited by
287
References
2
FWCI
6.60
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Curcumin inhibits cyclooxygenase-2 transcription in bile acid- and phorbol ester-treated human gastrointestinal epithelial cells. https://app.cochat.ai/papers/10.1093/carcin/20.3.445
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Zhang, F., Altorki, N. K., Mestre, J. R., Subbaramaiah, K., & Dannenberg, A. J. (1999). Curcumin inhibits cyclooxygenase-2 transcription in bile acid- and phorbol ester-treated human gastrointestinal epithelial cells. Carcinogenesis. https://doi.org/10.1093/carcin/20.3.445

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