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Sökning: WFRF:(Costantino Matteo) > (2022) > The deubiquitinase ...

The deubiquitinase USP8 regulates ovarian cancer cell response to cisplatin by suppressing apoptosis

Corno, Cristina (författare)
Dept Expt Oncol, Italy
D´arcy, Padraig (författare)
Karolinska Institutet,Linköpings universitet,Avdelningen för klinisk kemi och farmakologi,Medicinska fakulteten
Bagnoli, Marina (författare)
Dept Expt Oncol, Italy
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Paolini, Biagio (författare)
Fdn IRCCS Ist Nazl Tumori, Italy
Costantino, Matteo (författare)
Dept Expt Oncol, Italy
Carenini, Nives (författare)
Dept Expt Oncol, Italy
Corna, Elisabetta (författare)
Dept Expt Oncol, Italy
Alberti, Paola (författare)
Dept Expt Oncol, Italy
Mezzanzanica, Delia (författare)
Dept Expt Oncol, Italy
Colombo, Diego (författare)
Univ Milan, Italy
Linder, Stig (författare)
Linköpings universitet,Avdelningen för klinisk kemi och farmakologi,Medicinska fakulteten,Karolinska Inst, Sweden
Arrighetti, Noemi (författare)
Dept Expt Oncol, Italy
Perego, Paola (författare)
Dept Expt Oncol, Italy
visa färre...
 (creator_code:org_t)
2022-12-12
2022
Engelska.
Ingår i: Frontiers in Cell and Developmental Biology. - : FRONTIERS MEDIA SA. - 2296-634X. ; 10
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The identification of therapeutic approaches to improve response to platinum-based therapies is an urgent need for ovarian carcinoma. Deubiquitinases are a large family of ubiquitin proteases implicated in a variety of cellular functions and may contribute to tumor aggressive features through regulation of processes such as proliferation and cell death. Among the subfamily of ubiquitin-specific peptidases, USP8 appears to be involved in modulation of cancer cell survival by still poorly understood mechanisms. Thus, we used ovarian carcinoma cells of different histotypes, including cisplatin-resistant variants with increased survival features to evaluate the efficacy of molecular targeting of USP8 as a strategy to overcome drug resistance/modulate cisplatin response. We performed biochemical analysis of USP8 activity in pairs of cisplatin-sensitive and -resistant cells and found increased USP8 activity in resistant cells. Silencing of USP8 resulted in decreased activation of receptor tyrosine kinases and increased sensitivity to cisplatin in IGROV-1/Pt1 resistant cells as shown by colony forming assay. Increased cisplatin sensitivity was associated with enhanced cisplatin-induced caspase 3/7 activation and apoptosis, a phenotype also observed in cisplatin sensitive cells. Increased apoptosis was linked to FLIPL decrease and cisplatin induction of caspase 3 in IGROV-1/Pt1 cells, cisplatin-induced claspin and survivin down-regulation in IGROV-1 cells, thereby showing a decrease of anti-apoptotic proteins. Immunohistochemical staining on 65 clinical specimens from advanced stage ovarian carcinoma indicated that 40% of tumors were USP8 positive suggesting that USP8 is an independent prognostic factor for adverse outcome when considering progression free survival as a clinical end-point. Taken together, our results support that USP8 may be of diagnostic value and may provide a therapeutic target to improve the efficacy of platinum-based therapy in ovarian carcinoma.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

ovarian cancer; ubiquitin-specific protease 8; cisplatin; drug resistance; apoptosis

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