Your browser doesn't support javascript.
loading
Acetylshikonin Inhibits Human Pancreatic PANC-1 Cancer Cell Proliferation by Suppressing the NF-kappaB Activity
Biomolecules & Therapeutics ; : 428-433, 2015.
Article Dans Anglais | WPRIM | ID: wpr-36717
ABSTRACT
Acetylshikonin, a natural naphthoquinone derivative compound, has been used for treatment of inflammation and cancer. In the present study, we have investigated whether acetylshikonin could regulate the NF-kappaB signaling pathway, thereby leading to suppression of tumorigenesis. We observed that acetylshikonin significantly reduced proliferation of several cancer cell lines, including human pancreatic PANC-1 cancer cells. In addition, acetylshikonin inhibited phorbol 12-myristate 13-acetate (PMA) or tumor necrosis-alpha (TNF-alpha)-induced NF-kappaB reporter activity. Proteome cytokine array and real-time RT-PCR results illustrated that acetylshikonin inhibition of PMA-induced production of cytokines was mediated at the transcriptional level and it was associated with suppression of NF-kappaB activity and matrix metalloprotenases. Finally, we observed that an exposure of acetylshikonin significantly inhibited the anchorage-independent growth of PANC-1 cells. Together, our results indicate that acetylshikonin could serve as a promising therapeutic agent for future treatment of pancreatic cancer.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Tumeurs du pancréas / Lignée cellulaire / Cytokines / Facteur de transcription NF-kappa B / Protéome / Prolifération cellulaire / Carcinogenèse / Inflammation Limites du sujet: Humains langue: Anglais Texte intégral: Biomolecules & Therapeutics Année: 2015 Type: Article

Documents relatifs à ce sujet

MEDLINE

...
LILACS

LIS

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Tumeurs du pancréas / Lignée cellulaire / Cytokines / Facteur de transcription NF-kappa B / Protéome / Prolifération cellulaire / Carcinogenèse / Inflammation Limites du sujet: Humains langue: Anglais Texte intégral: Biomolecules & Therapeutics Année: 2015 Type: Article