Pregled bibliografske jedinice broj: 363291
The role of RhoB in lovastatin-induced reversion of cisplatin resistance in human laryngeal carcinoma cells
The role of RhoB in lovastatin-induced reversion of cisplatin resistance in human laryngeal carcinoma cells // Abstracts of the 33rd FEBS Congress and 11th IUBMB Conference
Cambridge: Wiley-Blackwell, 2008. str. 445-445 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
The role of RhoB in lovastatin-induced reversion of cisplatin resistance in human laryngeal carcinoma cells
Autori
Čimbora-Zovko, Tamara ; Fritz, Gerhard ; Osmak, Maja
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstracts of the 33rd FEBS Congress and 11th IUBMB Conference
/ - Cambridge : Wiley-Blackwell, 2008, 445-445
Skup
33rd FEBS Congress and 11th IUBMB Conference
Mjesto i datum
Atena, Grčka, 28.06.2008. - 03.07.2008
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
RhoB; cisplatin; drug-resistance; lovastatin
Sažetak
Introduction: Acquired resistance to cisplatin represents a major obstacle to successful chemotherapy. Our cisplatin-resistant CA3ST and CK2 cells display cytoskeleton alterations comparing to parental human laryngeal carcinoma HEp-2 cells. Since lipid modification of Rho GTPases is essential for biological function, we analyzed their expression as well as the cellular response to HMG-CoA reductase inhibitor lovastatin. Methods: We used semiquantitative RT-PCR and Western blot analysis, transient transfection, flow cytometry and cytotoxicity assays. Results: Among several Rho GTPases analyzed, cisplatin-resistant cells displayed strong decrease of RhoB on both mRNA and protein level. Lovastatin treatment induced concentration-dependent increase in RhoB in all cell lines tested and cell cycle arrest in G1 phase, which was more pronounced in cisplatin-resistant than parental cells, whereas at later time points cisplatin-resistant cells were highly susceptible to apoptosis. This effect was suppressed by the addition of geranylgeranyl pyrophosphate, and to less extent farnesyl pyrophosphate. Furthermore, lovastatin pretreatment restored sensitivity of resistant cells to cisplatin to the level found in parental cells. In line with this, transient transfection of EGFP-RhoB in CA3ST cells restored their sensitivity to cisplatin. Conclusions: We conclude that in cisplatin-resistant and lovastatin-sensitive laryngeal carcinoma cells RhoB is involved in resistance to cisplatin. Moreover, since lovastatin has already entered clinical trials for several types of cancer, these data could lead to new clinical strategies aimed to overcome cisplatin resistance and improve efficacy of cancer treatment.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
098-0982913-2748 - Stanični odgovor na citotoksične spojeve i razvoj otpornosti (Osmak, Maja, MZOS ) ( CroRIS)
098-0982913-2850 - Povećanje transdukcije adenovirusnih vektora i otpornost stanica na citostatike (Ambriović Ristov, Andreja, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb