Anticancer activities of curcumin on human Burkitt's lymphoma.
- Author:
Yong WU
1
;
Yuanzhong CHEN
;
Jianhua XU
;
Lianhuang LU
Author Information
- Publication Type:Journal Article
- MeSH: Antineoplastic Agents; pharmacology; Apoptosis; Burkitt Lymphoma; Cell Cycle; drug effects; Cell Division; drug effects; Curcumin; pharmacology; Gene Expression Regulation; drug effects; Humans; Proto-Oncogene Proteins c-bcl-2; biosynthesis; genetics; Proto-Oncogene Proteins c-myc; biosynthesis; genetics; Tumor Cells, Cultured; Tumor Suppressor Protein p53; biosynthesis; genetics; fas Receptor; biosynthesis; genetics
- From: Chinese Journal of Oncology 2002;24(4):348-352
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo study the anticancer activities of curcumin on human Burkitt's lymphoma and their molecular mechanism.
METHODSThe effect of curcumin on the growth of CA46 cells and apoptosis were studied through Trypan blue exclusion, MTT assay, cell cycle, DNA fragmentation analysis and detection of TdT-mediated dUTP nick end labeling (TUNEL). The effect of curcumin on the expression of c-myc, bcl-2, mutant-type p53 and Fas protein and mRNA was studied by flow cytometry (FCM) and reverse transcription-polymerase chain reaction (RT-PCR).
RESULTS1. Curcumin inhibited proliferation of CA46 cells in a time- and dose-dependent manner, 2. CA46 cells treated with curcumin showed G(0)/G(1) or G(2)/M phase increase and S phase decrease, 3. CA46 cells apoptosis induced by curcumin was confirmed by DNA fragmentation and TUNEL and 4. The expression of c-myc, bcl-2, mutant-type p53 protein and mRNA was decreased sharply in CA46 cells treated with curcumin, while Fas protein and mRNA was increased.
CONCLUSIONCurcumin is able to inhibit the proliferation of CA46 cells and induce the cell apoptosis by down-regulating the expression of c-myc, bcl-2, mutant-type p53 and up-regulating the expression of Fas.
