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Abstract Title:

Novel TRAIL sensitizer Taraxacum officinale F.H. Wigg enhances TRAIL-induced apoptosis in Huh7 cells.

Abstract Source:

Mol Carcinog. 2015 Feb 3. Epub 2015 Feb 3. PMID: 25647515

Abstract Author(s):

Ji-Yong Yoon, Hyun-Soo Cho, Jeong-Ju Lee, Hyo-Jung Lee, Soo Young Jun, Jae-Hye Lee, Hyuk-Hwan Song, SangHo Choi, Vassiliki Saloura, Choon Gil Park, Cheol-Hee Kim, Nam-Soon Kim

Article Affiliation:

Ji-Yong Yoon

Abstract:

TRAIL (TNF-related apoptosis inducing ligand) is a promising anti-cancer drug target that selectively induces apoptosis in cancer cells. However, many cancer cells are resistant to TRAIL-induced apoptosis. Therefore, reversing TRAIL resistance is an important step for the development of effective TRAIL-based anti-cancer therapies. We previously reported that knockdown of the TOR signaling pathway regulator-like (TIPRL) protein caused TRAIL-induced apoptosis by activation of the MKK7-c-Jun N-terminal Kinase (JNK) pathway through disruption of the MKK7-TIPRL interaction. Here, we identified Taraxacum officinale F.H. Wigg (TO) as a novel TRAIL sensitizer from a set of 500 natural products using an ELISA system and validated its activity by GST pull-down analysis. Furthermore, combination treatment of Huh7 cells with TRAIL and TO resulted in TRAIL-induced apoptosis mediated through inhibition of the MKK7-TIPRL interaction and subsequent activation of MKK7-JNK phosphorylation. Interestingly, HPLC analysis identified chicoric acid as a major component of the TO extract, and combination treatment with chicoric acid and TRAIL induced TRAIL-induced cell apoptosis via JNK activation due to inhibition of the MKK7-TIPRL interaction. Our results suggest that TO plays an important role in TRAIL-induced apoptosis, and further functional studies are warranted to confirm the importance of TO as a novel TRAIL sensitizer for cancer therapy.© 2015 Wiley Periodicals, Inc.

Study Type : In Vitro Study

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Sayer Ji
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