Park Sang Eun, Park Cheol, Kim Sun Hee, Hossain Mohammad Akbar, Kim Min Young, Chung Hae Young, Son Woo Sung, Kim Gi-Young, Choi Yung Hyun, Kim Nam Deuk
Department of Pharmacy (BK21 Program), Research Institute for Drug Development, Pusan National University, Busan 609-735, Republic of Korea.
J Ethnopharmacol. 2009 Jan 21;121(2):304-12. doi: 10.1016/j.jep.2008.10.038. Epub 2008 Nov 12.
Korean red ginseng (KRG, Panax ginseng C.A. Meyer Radix rubra) has been used to treat various diseases including cancer. However, the molecular mechanisms responsible for KRG extract induced apoptosis and telomerase inhibition remain unclear.
The hot water extract from KRG was used to evaluate the mechanism of induction of apoptosis in U937 human leukemia cells and its effects on cyclooxgenase-2 (COX-2) and telomerase activity.
KRG extract treatment to U937 cells resulted in growth inhibition and induction of apoptosis in a concentration-dependent manner as measured by hemacytometer counts, MTT assay, fluorescence microscopy, agarose gel electrophoresis and flow cytometry analysis. The increase in apoptosis was associated with the down-regulation of antiapoptotic Bcl-2, Bcl-X(L), and IAPs family members, and the activation of caspase-3. KRG extract treatment also decreased the expression levels of COX-2 and inducible nitric oxide synthase. Furthermore, KRG extract treatment progressively down-regulated the expression of human telomerase reverse transcriptase, a main determinant of the telomerase enzymatic activity, with inhibiting the expression of c-Myc in a concentration-dependent manner.
These results provide important new insights into the possible molecular mechanisms of the anticancer activity of KRG extract.
韩国红参(KRG,人参C.A.迈耶红参)已被用于治疗包括癌症在内的各种疾病。然而,KRG提取物诱导细胞凋亡和抑制端粒酶的分子机制仍不清楚。
使用KRG的热水提取物评估其诱导U937人白血病细胞凋亡的机制及其对环氧合酶-2(COX-2)和端粒酶活性的影响。
通过血细胞计数器计数、MTT法、荧光显微镜、琼脂糖凝胶电泳和流式细胞术分析测定,用KRG提取物处理U937细胞导致生长抑制并以浓度依赖方式诱导细胞凋亡。细胞凋亡增加与抗凋亡Bcl-2、Bcl-X(L)和IAPs家族成员的下调以及caspase-3的激活有关。KRG提取物处理还降低了COX-2和诱导型一氧化氮合酶的表达水平。此外,KRG提取物处理逐渐下调人端粒酶逆转录酶的表达,端粒酶逆转录酶是端粒酶活性的主要决定因素,并以浓度依赖方式抑制c-Myc的表达。
这些结果为KRG提取物抗癌活性的可能分子机制提供了重要的新见解。