Pingyangmycin and Bleomycin Share the Same Cytotoxicity Pathway

被引:32
作者
He, Yanli [1 ,2 ]
Lan, Ying [1 ]
Liu, Yong [1 ]
Yu, Haibo [3 ]
Han, Zhangrun [1 ]
Li, Xiulian [1 ]
Zhang, Lijuan [1 ,2 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, 5 Yushan Rd, Qingdao 266003, Peoples R China
[2] Qingdao Univ, Inst Cerebrovasc Dis, Affiliated Hosp, Qingdao 266003, Peoples R China
[3] Northwest A&F Univ, Coll Anim Sci & Technol, Xianyang 712100, Peoples R China
关键词
bleomycin A2; bleomycin B2; bleomycin A5 or pingyangmycin; cytotoxicity; cell cycle; apoptosis; GROWTH-FACTOR RECEPTOR; HEPARAN-SULFATE; SACCHAROMYCES-CEREVISIAE; LUNG-CANCER; PERSONALIZED MEDICINE; PROTECTIVE MECHANISMS; CELLULAR-RESISTANCE; UP-REGULATION; JURKAT CELLS; GLYCOSAMINOGLYCANS;
D O I
10.3390/molecules21070862
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
Pingyangmycin is an anticancer drug known as bleomycin A5 (A5), discovered in the Pingyang County of Zhejiang Province of China. Bleomycin (BLM) is a mixture of mainly two compounds (A2 and B2), which is on the World Health Organization's list of essential medicines. Both BLM and A5 are hydrophilic molecules that depend on transporters or endocytosis receptors to get inside of cells. Once inside, the anticancer activities rely on their abilities to produce DNA breaks, thus leading to cell death. Interestingly, the half maximal inhibitory concentration (IC50) of BLMs in different cancer cell lines varies from nM to M ranges. Different cellular uptake, DNA repair rate, and/or increased drug detoxification might be some of the reasons; however, the molecules and signaling pathways responsible for these processes are largely unknown. In the current study, we purified the A2 and B2 from the BLM and tested the cytotoxicities and the molecular mechanisms of each individual compound or in combination with six different cell lines, including a Chinese hamster ovary (CHO) cell line defective in glycosaminoglycan biosynthesis. Our data suggested that glycosaminoglycans might be involved in the cellular uptake of BLMs. Moreover, both BLM and A5 shared similar signaling pathways and are involved in cell cycle and apoptosis in different cancer cell lines.
引用
收藏
页数:15
相关论文
共 67 条
[1]  
[Anonymous], 2015, WHO model list of essential medicines, 19th list
[2]   A genome-wide screen in Saccharomyces cerevisiae reveals altered transport as a mechanism of resistance to the anticancer drug bleomycin [J].
Aouida, M ;
Pagé, N ;
Leduc, A ;
Peter, M ;
Ramotar, D .
CANCER RESEARCH, 2004, 64 (03) :1102-1109
[3]   Comparative roles of the cell wall and cell membrane in limiting uptake of xenobiotic molecules by Saccharomyces cerevisiae [J].
Aouida, M ;
Tounekti, O ;
Belhadj, O ;
Mir, LM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (06) :2012-2014
[4]   A New Twist in Cellular Resistance to the Anticancer Drug Bleomycin-A5 [J].
Aouida, Mustapha ;
Ramotar, Dindial .
CURRENT DRUG METABOLISM, 2010, 11 (07) :595-602
[5]   The Human Carnitine Transporter SLC22A16 Mediates High Affinity Uptake of the Anticancer Polyamine Analogue Bleomycin-A5 [J].
Aouida, Mustapha ;
Poulin, Richard ;
Ramotar, Dindial .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (09) :6275-6284
[6]  
Aouida M, 2009, BIOCHEM CELL BIOL, V87, P653, DOI [10.1139/O09-045, 10.1139/o09-045]
[7]   Secreted NS1 of dengue virus attaches to the surface of cells via interactions with heparan sulfate and chondroitin sulfate E [J].
Avirutnan, Panisadee ;
Zhang, Lijuan ;
Punyadee, Nuntaya ;
Manuyakorn, Ananya ;
Puttikhunt, Chunya ;
Kasinrerk, Watchara ;
Malasit, Prida ;
Atkinson, John P. ;
Diamond, Michael S. .
PLOS PATHOGENS, 2007, 3 (11) :1798-1812
[8]  
BELEHRADEK J, 1994, BBA-BIOMEMBRANES, V1190, P155
[9]   Tumor attenuation by combined heparan sulfate and polyamine depletion [J].
Belting, M ;
Borsig, L ;
Fuster, MM ;
Brown, JR ;
Persson, L ;
Fransson, LÅ ;
Esko, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :371-376
[10]   Complementation of the Yeast Model System Reveals that Caenorhabditis elegans OCT-1 Is a Functional Transporter of Anthracyclines [J].
Brosseau, Nicolas ;
Andreev, Emil ;
Ramotar, Dindial .
PLOS ONE, 2015, 10 (07)