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Journal of Applied Pharmaceutical ScienceVolume 5, Issue 8, 2015, Pages 1-5

2-methoxy-1,4-naphthoquinone (MNQ) Suppresses Protein Kinase C ßI, δ, and ζ expression in Raji

cells

(Article)

Yew, W.T.,

Kitson, L.,

Hock, A.H.S.,

Chiew, G.S.,

Mooi, L.Y.

View Correspondence (jump link)

aDepartment of Pre-Clinical Sciences, Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman, Lot PT 21144, Jalan Sungai Long, Bandar Sungai Long, Kajang, Selangor, Malaysia

bSchool of Biosciences, Taylor's University, Lakeside Campus 1, Jalan Taylor's, Subang Jaya, Selangor, Malaysia

Abstract

Protein Kinase C (PKC) is widely documented to be involved in the regulation of cancer cell growth, proliferation, survival, inflammation and apoptosis. This study evaluates the capability of 2-Methoxy-1,4-Naphthoquinone (MNQ) in regulating PMA-induced PKC expression in human Burkitt's lymphoma cell line (Raji cells).

MNQ exhibited stronger anti-tumour-promoting activity than genistein based on the inhibitory assay of Epstein-Barr virus (EBV) activation. The IC50 values attained were 2.92 and 7.40 μM, respectively. The suppressive effects of MNQ on PKC expression was determined by using the PepTag® non-radioactive detection of PKC assay. The IC50 values achieved for staurosporine and rottlerin (standard control), and MNQ were 0.01, 6.38, and 13.13 μM, respectively. These preliminary results indicate that MNQ specifically suppressed the expression of PKC ßI, δ, and ζ in a concentration-dependent manner in Raji cells. © 2015 Wong Teck Yew et al.

Author keywords

2-Methoxy-1,4-Naphthoquinone

Antitumour-promoting

Cancer chemoprevention

Protein kinase C

(2)

ISSN: 22313354

Source Type: Journal

Original language: English

DOI: 10.7324/JAPS.2015.50801

Document Type: Article

Publisher: Open Science Publishers LLP Inc.

Mooi, L.Y.; Department of Pre-Clinical Sciences, Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman, Lot PT 21144, Jalan Sungai Long, Bandar Sungai Long, Kajang, Selangor, Malaysia

© Copyright 2015 Elsevier B.V., All rights reserved.

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