Kunitz type protease inhibitor EgKI-1 from the canine tapeworm Echinococcus granulosus as a promising therapeutic against breast cancer

被引:33
作者
Ranasinghe, Shiwanthi L. [1 ]
Boyle, Glen M. [2 ]
Fischer, Katja [3 ]
Potriquet, Jeremy [4 ]
Mulvenna, Jason P. [5 ]
McManus, Donald P. [1 ]
机构
[1] QIMR Berghofer Med Res Inst, Immunol Dept, Mol Parasitol Lab, Brisbane, Qld, Australia
[2] QIMR Berghofer Med Res Inst, Cell & Mol Biol Dept, Canc Drug Mech Grp, Brisbane, Qld, Australia
[3] QIMR Berghofer Med Res Inst, Cell & Mol Biol Dept, Scabies Grp, Brisbane, Qld, Australia
[4] James Cook Univ, Australian Inst Trop Hlth & Med, Cairns, Australia
[5] QIMR Berghofer Med Res Inst, Biomarkers & Biol Infect Related Cancers Lab, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
CELL; NEUTROPHILS; PEGYLATION; MIGRATION; PROTEINS; DRUGS; ASSAY;
D O I
10.1371/journal.pone.0200433
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
EgKI-1, a member of the Kunitz type protease inhibitor family, is highly expressed by the oncosphere of the canine tapeworm Echinococcus granulosus, the stage that is infectious to humans and ungulates, giving rise to a hydatid cyst localized to the liver and other organs. Larval protoscoleces, which develop within the hydatid cyst, have been shown to possess anti-cancer properties, although the precise molecules involved have not been identified. We show that recombinant EgKI-1 inhibits the growth and migration of a range of human cancers including breast, melanoma and cervical cancer cell lines in a dose-dependent manner in vitro without affecting normal cell growth. Furthermore, EgKI-1 treatment arrested the cancer cell growth by disrupting the cell cycle and induced apoptosis of cancer cells in vitro. An in vivo model of triple negative breast cancer (MDA-MB-231) in BALB/c nude mice showed significant tumor growth reduction in EgKI-1-treated mice compared with controls. These findings indicate that EgKI-1 shows promise for future development as an anti-cancer therapeutic.
引用
收藏
页数:16
相关论文
共 47 条
[1]   A recombinant protein based on Trypanosoma cruzi surface molecule gp82 induces apoptotic cell death in melanoma cells [J].
Atayde, Vanessa D. ;
Jasiulionis, Miriam G. ;
Cortez, Mauro ;
Yoshida, Nobuko .
MELANOMA RESEARCH, 2008, 18 (03) :172-183
[2]   Potential of apoptotic pathway-targeted cancer therapeutic research: Where do we stand? [J].
Baig, S. ;
Seevasant, I. ;
Mohamad, J. ;
Mukheem, A. ;
Huri, H. Z. ;
Kamarul, T. .
CELL DEATH & DISEASE, 2016, 7 :e2058-e2058
[3]   Scabies Mite Inactivated Serine Protease Paralogs Inhibit the Human Complement System [J].
Bergstrom, Frida C. ;
Reynolds, Simone ;
Johnstone, Masego ;
Pike, Robert N. ;
Buckle, Ashley M. ;
Kemp, David J. ;
Fischer, Katja ;
Blom, Anna M. .
JOURNAL OF IMMUNOLOGY, 2009, 182 (12) :7809-7817
[4]   Intra-Lesional Injection of the Novel PKC Activator EBC-46 Rapidly Ablates Tumors in Mouse Models [J].
Boyle, Glen M. ;
D'Souza, Marjorie M. A. ;
Pierce, Carly J. ;
Adams, Ryan A. ;
Cantor, Aaron S. ;
Johns, Jenny P. ;
Maslovskaya, Lidia ;
Gordon, Victoria A. ;
Reddell, Paul W. ;
Parsons, Peter G. .
PLOS ONE, 2014, 9 (10)
[5]   Mitosis-targeted anti-cancer therapies: where they stand [J].
Chan, K-S ;
Koh, C-G ;
Li, H-Y .
CELL DEATH & DISEASE, 2012, 3 :e411-e411
[6]   Neutrophils in cancer: neutral no more [J].
Coffelt, Seth B. ;
Wellenstein, Max D. ;
de Visser, Karin E. .
NATURE REVIEWS CANCER, 2016, 16 (07) :431-446
[7]  
Comsa S, 2015, ANTICANCER RES, V35, P3147
[8]   Echinococcosis: disease, detection and transmission [J].
Craig, PS ;
Rogan, MT ;
Campos-Ponce, M .
PARASITOLOGY, 2003, 127 :S5-S20
[9]   The Future of Peptide-based Drugs [J].
Craik, David J. ;
Fairlie, David P. ;
Liras, Spiros ;
Price, David .
CHEMICAL BIOLOGY & DRUG DESIGN, 2013, 81 (01) :136-147
[10]   Mycoplasma contamination of cell cultures: Incidence, sources, effects, detection, elimination, prevention [J].
Drexler, HG ;
Uphoff, CC .
CYTOTECHNOLOGY, 2002, 39 (02) :75-90