Pregled bibliografske jedinice broj: 1274388
Euchromatic Histone Lysine Methyltransferase 2 Inhibition Enhances Carfilzomib Sensitivity and Overcomes Drug Resistance in Multiple Myeloma Cell Lines
Euchromatic Histone Lysine Methyltransferase 2 Inhibition Enhances Carfilzomib Sensitivity and Overcomes Drug Resistance in Multiple Myeloma Cell Lines // Cancers, 15 (2023), 8; 37190128, 16 doi:10.3390/cancers15082199 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1274388 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Euchromatic Histone Lysine Methyltransferase 2
Inhibition Enhances Carfilzomib Sensitivity and
Overcomes Drug Resistance in Multiple Myeloma Cell
Lines
Autori
Mereu, Elisabetta ; Abbo, Damiano ; Paradžik, Tina ; Cumerlato, Michela ; Bandini, Cecilia ; Labrador, Maria ; Maccagno, Monica ; Ronchetti, Domenica ; Manicardi, Veronica ; Neri, Antonino ; Piva, Roberto
Izvornik
Cancers (2072-6694) 15
(2023), 8;
37190128, 16
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
EHMT2 ; combinatorial treatment ; drug resistance ; functional screening ; multiple myeloma ; proteasome inhibitors
Sažetak
Proteasome inhibitors (PIs) are extensively used for the therapy of multiple myeloma. However, patients continuously relapse or are intrinsically resistant to this class of drugs. In addition, adverse toxic effects such as peripheral neuropathy and cardiotoxicity could arise. Here, to identify compounds that can increase the efficacy of PIs, we performed a functional screening using a library of small-molecule inhibitors covering key signaling pathways. Among the best synthetic lethal interactions, the euchromatic histone-lysine N-methyltransferase 2 (EHMT2) inhibitor UNC0642 displayed a cooperative effect with carfilzomib (CFZ) in numerous multiple myeloma (MM) cell lines, including drug-resistant models. In MM patients, EHMT2 expression correlated to worse overall and progression-free survival. Moreover, EHMT2 levels were significantly increased in bortezomib-resistant patients. We demonstrated that CFZ/UNC0642 combination exhibited a favorable cytotoxicity profile toward peripheral blood mononuclear cells and bone-marrow-derived stromal cells. To exclude off-target effects, we proved that UNC0642 treatment reduces EHMT2-related molecular markers and that an alternative EHMT2 inhibitor recapitulated the synergistic activity with CFZ. Finally, we showed that the combinatorial treatment significantly perturbs autophagy and the DNA damage repair pathways, suggesting a multi- layered mechanism of action. Overall, the present study demonstrates that EHMT2 inhibition could provide a valuable strategy to enhance PI sensitivity and overcome drug resistance in MM patients.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus