| Literature DB >> 33668794 |
Pawel Robak1, Dariusz Jarych2,3, Damian Mikulski4, Izabela Dróżdż5, Edyta Węgłowska2, Aleksandra Kotkowska6, Małgorzata Misiewicz6, Piotr Smolewski1, Konrad Stawiski4, Wojciech Fendler4, Janusz Szemraj7, Tadeusz Robak6.
Abstract
Proteasome inhibitors, like bortezomib, play a key role in the treatment of multiple myeloma (MM); however, most patients eventually relapse and eventually show multiple drug resistance, and the molecular mechanisms of this resistance remain unclear. The aim of our study is to assess the expression of previously described genes that may influence the resistance to bortezomib treatment at the mRNA level (ABCB1, CXCR4, MAF, MARCKS, POMP, PSMB5, RPL5, TXN, and XBP1) and prognosis of MM patients. mRNA expression was determined in 73 MM patients treated with bortezomib-based regimens (30 bortzomib-sensitive and 43 bortezomib-refractory patients) and 11 healthy controls. RPL5 was significantly down-regulated in multiple myeloma patients as compared with healthy controls. Moreover, POMP was significantly up-regulated in MM patients refractory to bortezomib-based treatment. In multivariate analysis, high expression of PSMB5 and CXCR and autologous stem cell transplantation were independent predictors of progression-free survival, and high expression of POMP and RPL5 was associated with shorter overall survival.Entities:
Keywords: CXCR4; POMP; PSMB5; RPL5; TXN; XBP1; bortezomib; gene expression; multiple myeloma; refractory
Year: 2021 PMID: 33668794 DOI: 10.3390/cancers13050951
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639