Cartilage polysaccharide induces apoptosis in K562 cells through a reactive oxygen species-mediated caspase pathway

被引:1
作者
Song, Wei [1 ]
Hu, Panpan [1 ]
Shan, Yujuan [1 ]
Du, Ming [1 ]
Liu, Anjun [2 ]
Ye, Ran [3 ]
机构
[1] Harbin Inst Technol, Sch Food Sci & Engn, Harbin 150090, Peoples R China
[2] Tianjin Univ Sci & Technol, Minist Educ, Key Lab Food Nutr & Safety, Tianjin 300457, Peoples R China
[3] Univ Tennessee, Dept Biosyst Engn & Soil Sci, Knoxville, TN 37996 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
BREAST-CANCER CELLS; ANTITUMOR-ACTIVITY; SIGNALING PATHWAY; BOLETUS-EDULIS; GLIOMA-CELLS; DNA-DAMAGE; MITOCHONDRIAL; ROS; ANTIOXIDANT; ACTIVATION;
D O I
10.1039/c4fo00476k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a polysaccharide (PS) was successfully extracted from porcine cartilage and its effect on chronic myeloid leukemia was examined using human K562 cells. The results of cell proliferation assays indicated that the PS inhibited cancer cell growth at different concentrations. Morphological and biochemical changes characteristic of apoptosis were observed and confirmed by PI staining and TUNEL assay. The nuclear DNA, RNA and proteins of the cancer cells subjected to PS treatment were irreversibly destroyed by reactive oxygen species (ROS), additionally, the ROS effected on the cells directly. The apoptotic signals altered the permeability of the mitochondrial outer membrane, thereby resulted in the release of apoptotic factors into the cytoplasm that induced apoptosis. As caspase-3/7, 8 and 9 were expressed, it was speculated that both intrinsic and extrinsic pathways were involved in the PS-induced apoptosis.
引用
收藏
页码:2486 / 2493
页数:8
相关论文
共 37 条
[1]   ALCAPs induce mitochondrial apoptosis and activate DNA damage response by generating ROS and inhibiting topoisomerase I enzyme activity in K562 leukemia cell line [J].
Bogurcu, Nuray ;
Sevimli-Gur, Canan ;
Ozmen, Besra ;
Bedir, Erdal ;
Korkmaz, Kemal Sami .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 409 (04) :738-744
[2]   The cell cycle is a redox cycle: Linking phase-specific targets to cell fate [J].
Burhans, William C. ;
Heintz, Nicholas H. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 47 (09) :1282-1293
[3]   Intestinal redox biology and oxidative stress [J].
Circu, Magdalena L. ;
Aw, Tak Yee .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2012, 23 (07) :729-737
[4]   Determining the contributions of caspase-2, caspase-8 and effector caspases to intracellular VDVADase activities during apoptosis initiation and execution [J].
Delgado, M. Eugenia ;
Olsson, Magnus ;
Lincoln, Frank A. ;
Zhivotovsky, Boris ;
Rehm, Markus .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2013, 1833 (10) :2279-2292
[5]   Mitochondria as a Source of Reactive Oxygen and Nitrogen Species: From Molecular Mechanisms to Human Health [J].
Figueira, Tiago R. ;
Barros, Mario H. ;
Camargo, Anamaria A. ;
Castilho, Roger F. ;
Ferreira, Julio C. B. ;
Kowaltowski, Alicia J. ;
Sluse, Francis E. ;
Souza-Pinto, Nadja C. ;
Vercesi, Anibal E. .
ANTIOXIDANTS & REDOX SIGNALING, 2013, 18 (16) :2029-2074
[6]   PROTEOGLYCANS - MANY FORMS AND MANY FUNCTIONS [J].
HARDINGHAM, TE ;
FOSANG, AJ .
FASEB JOURNAL, 1992, 6 (03) :861-870
[7]   Intracellular redox status controls membrane localization of pro- and anti-migratory signaling molecules [J].
Hempel, Nadine ;
Melendez, J. Andres .
REDOX BIOLOGY, 2014, 2 :245-250
[8]   Arctigenin, a dietary phytoestrogen, induces apoptosis of estrogen receptor-negative breast cancer cells through the ROS/p38 MAPK pathway and epigenetic regulation [J].
Hsieh, Chia-Jung ;
Kuo, Po-Lin ;
Hsu, Ying-Chan ;
Huang, Ya-Fang ;
Tsai, Eing-Mei ;
Hsu, Ya-Ling .
FREE RADICAL BIOLOGY AND MEDICINE, 2014, 67 :159-170
[9]   Recent advances in apoptosis, mitochondria and drug resistance in cancer cells [J].
Indran, Inthrani R. ;
Tufo, Gregory ;
Pervaiz, Shazib ;
Brenner, Catherine .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2011, 1807 (06) :735-745
[10]   Eupalmerin acetate, a novel anticancer agent from Caribbean gorgonian octocorals, induces apoptosis in malignant glioma cells via the c-Jun NH2-terminal kinase pathway [J].
Iwamaru, Arifumi ;
Iwado, Eiji ;
Kondo, Seiji ;
Newman, Robert A. ;
Vera, Burnilda ;
Rodriguez, Abimael D. ;
Kondo, Yasuko .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (01) :184-192