Abstract
Capsaicin, the principal pungent ingredient of hot chili peppers, has anti-inflammatory and analgesic properties and is currently used as a topical cream for the management of various neuropathic conditions. In the present study, topical application of capsaicin onto dorsal skin of female ICR mice strongly suppressed phorbol ester-stimulated activation of NF-κB via blockade of IκB-α degradation with subsequent inhibition of nuclear translocation of the functionally active NF-κB subunit, p65. Likewise, phorbol ester-induced activation of activator protein-1 (AP-1) was abolished by capsaicin pretreatment. Since altered transactivation of NF-κB and AP-1 has been implicated for neoplastic transformation and progression, the suppression of these transcription factors by capsaicin may account for its previously reported chemopreventive effects on mouse skin tumorigenesis as well as inflammation.
Original language | English |
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Pages (from-to) | 119-126 |
Number of pages | 8 |
Journal | Cancer Letters |
Volume | 164 |
Issue number | 2 |
DOIs | |
State | Published - 26 Mar 2001 |
Keywords
- Activator protein 1
- Capsaicin
- Mouse skin carcinogenesis
- NF-κB
- Transcription factor
- Tumor promotion