NEHYBOVÁ, Tereza, Jan ŠMARDA, Lukáš DANIEL, Marek STIBOREK, Viktor KANICKÝ, Ivan SPASOJEVIČ, Jan PREISLER, Jiří DAMBORSKÝ and Petr BENEŠ. Wedelolactone Acts as Proteasome Inhibitor in Breast Cancer Cells. International Journal of Molecular Sciences. Basel: MDPI, 2017, vol. 18, No 4, p. nestránkováno, 14 pp. ISSN 1422-0067. Available from: https://dx.doi.org/10.3390/ijms18040729.
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Basic information
Original name Wedelolactone Acts as Proteasome Inhibitor in Breast Cancer Cells
Authors NEHYBOVÁ, Tereza (203 Czech Republic, belonging to the institution), Jan ŠMARDA (203 Czech Republic, belonging to the institution), Lukáš DANIEL (203 Czech Republic, belonging to the institution), Marek STIBOREK (203 Czech Republic, belonging to the institution), Viktor KANICKÝ (203 Czech Republic, belonging to the institution), Ivan SPASOJEVIČ (688 Serbia), Jan PREISLER (203 Czech Republic, belonging to the institution), Jiří DAMBORSKÝ (203 Czech Republic, belonging to the institution) and Petr BENEŠ (203 Czech Republic, belonging to the institution).
Edition International Journal of Molecular Sciences, Basel, MDPI, 2017, 1422-0067.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.687
RIV identification code RIV/00216224:14310/17:00094712
Organization unit Faculty of Science
Doi http://dx.doi.org/10.3390/ijms18040729
UT WoS 000402639400055
Keywords in English breast cancer; copper; proteasome; reactive oxygen species; wedelolactone
Tags NZ, rivok
Tags International impact, Reviewed
Changed by Changed by: Ing. Nicole Zrilić, učo 240776. Changed: 13/4/2018 08:45.
Abstract
Wedelolactone is a multi-target natural plant coumestan exhibiting cytotoxicity towards cancer cells. Although several molecular targets of wedelolactone have been recognized, the molecular mechanism of its cytotoxicity has not yet been elucidated. In this study, we show that wedelolactone acts as an inhibitor of chymotrypsin-like, trypsin-like, and caspase-like activities of proteasome in breast cancer cells. The proteasome inhibitory effect of wedelolactone was documented by (i) reduced cleavage of fluorogenic proteasome substrates; (ii) accumulation of polyubiquitinated proteins and proteins with rapid turnover in tumor cells; and (iii) molecular docking of wedelolactone into the active sites of proteasome catalytic subunits. Inhibition of proteasome by wedelolactone was independent on its ability to induce reactive oxygen species production by redox cycling with copper ions, suggesting that wedelolactone acts as copper-independent proteasome inhibitor. We conclude that the cytotoxicity of wedelolactone to breast cancer cells is partially mediated by targeting proteasomal protein degradation pathway. Understanding the structural basis for inhibitory mode of wedelolactone might help to open up new avenues for design of novel compounds efficiently inhibiting cancer cells.
Links
GA15-05387S, research and development projectName: Laserově desorpční hmotnostní spektrometrie pro analýzu molekul a nanočástic
Investor: Czech Science Foundation
LO1214, research and development projectName: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX)
Investor: Ministry of Education, Youth and Sports of the CR
LQ1601, research and development projectName: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR
MUNI/A/0967/2015, interní kód MUName: Podpora výzkumné činnosti studentů molekulární biologie a genetiky 4 (Acronym: MBG4)
Investor: Masaryk University, Category A
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