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1.
Cancer Chemother Pharmacol ; 89(4): 431-440, 2022 04.
Article in English | MEDLINE | ID: mdl-35190872

ABSTRACT

PURPOSE: Platinum-containing therapy is standard treatment for relapsed Diffuse Large B-Cell Lymphoma (DLBCL). However, the efficacy of treatment is limited by drug resistance leading to relapse. Cisplatin resistance has been linked to impairments of the DNA damage response, and several DNA repair proteins have been identified as clients of the molecular chaperone Hsp90. Here, we investigated the combinatory treatment of cisplatin and the Hsp90 inhibitor, 17AAG, in DLBCL cells to evaluate if inhibition of Hsp90 could sensitize DLBCL cells to cisplatin treatment. METHODS: Cell viability was assessed for cisplatin and 17AAG as monotherapies and for 25 different combinations in 7 DLBCL cell lines, where the Bliss Independence Model and the Combination Index were applied to assess their interaction. Induction of apoptosis and DNA damage response were evaluated by measuring Annexin V and γH2AX levels after 48 h of exposure. RESULTS: 17AAG synergized with cisplatin in DLBCL cells as detected in both interaction assessment models, resulting in a lower viability after 48 h for the combination-treated cells compared to both vehicle and single drug-treated cells. The combination also induced a stronger apoptotic response and an increase in DNA damage in 17AAG, cisplatin- and combination-treated cells compared to vehicle-treated cells, with the effect of the combination generally being higher than compared to both single drugs. CONCLUSION: This study demonstrates that 17AAG sensitizes DLBCL cells to cisplatin treatment. This effect is correlated with increased apoptotic and DNA damage response, potentially mediated by downregulation of Hsp90 clients in DNA repair pathways. Thus, cisplatin resistance could plausibly be overcome by combining the treatment with an Hsp90 inhibiting drug.


Subject(s)
Antineoplastic Agents , Lymphoma, Large B-Cell, Diffuse , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Apoptosis , Benzoquinones/pharmacology , Cell Line, Tumor , Cisplatin/pharmacology , Cisplatin/therapeutic use , HSP90 Heat-Shock Proteins , Humans , Lactams, Macrocyclic/pharmacology , Lymphoma, Large B-Cell, Diffuse/drug therapy , Lymphoma, Large B-Cell, Diffuse/pathology , Neoplasm Recurrence, Local/drug therapy
2.
Cancer Drug Resist ; 4(1): 208-222, 2021.
Article in English | MEDLINE | ID: mdl-35582014

ABSTRACT

Aim: Bendamustine is primarily used for treatment of indolent lymphomas but has shown efficacy in some patients with diffuse large B-cell lymphoma (DLBCL) and multiple myeloma (MM). Molecular-based patient stratification for identification of resistant patients, who will benefit from alternative treatments, is important. The aim of this study was to develop a resistance gene signature (REGS) from bendamustine dose-response assays in cultures of DLBCL and MM cell lines, enabling prediction of bendamustine response in DLBCL and MM patients. Methods: Bendamustine response was determined in 14 DLBCL and 11 MM cell lines. Using baseline gene expression profiles and degree of growth inhibition after bendamustine exposure, a bendamustine REGS was developed and examined for the risk stratification potential in DLBCL (n = 971) and MM (n = 1,126) patients divided into prognostic subtypes. Results: Bendamustine resistance significantly correlated with resistance to cyclophosphamide in DLBCL and melphalan in MM cell lines. The bendamustine REGS showed significantly lower bendamustine resistance probabilities in DLBCL patients with GCB subtype tumors and in tumors of the differentiation dependent centrocyte and plasmablast subtypes. In MM patients, pre-BII classified tumors displayed high bendamustine resistance probabilities and the plasma cell subtype had lower bendamustine resistance probability than memory cells. Furthermore, tumors belonging to the 4p14, MAF, and D2 TC subclasses consistently displayed high bendamustine resistance probabilities. Conclusion: Significant differences in predicted response to bendamustine were found in molecular subtypes of DLBCL and MM, encouraging validation in prospective bendamustine-treated cohorts with available gene expression profiles and follow-up data.

3.
IEEE Trans Med Imaging ; 39(4): 1085-1093, 2020 04.
Article in English | MEDLINE | ID: mdl-32054570

ABSTRACT

A capacitive impedance metasurface combined with a transceiver coil to improve the radio frequency magnetic field for 1.5T magnetic resonance imaging applications is presented. The novel transceiver provides localized enhancement in magnetic flux density when compared to a transceiver coil alone by incorporating an electrically small metasurface using an interdigital capacitance approach. Full field simulations employing the metasurface show a significant improvement in magnetic flux density inside a homogeneous dielectric phantom, which is also shown to perform well for a range of depths into the phantom. The concept was experimentally demonstrated through vector network analyzer measurements and images have been taken using a 1.5T MRI scanner. The results show there is a 216% improvement in transmission efficiency, a 133% improvement in receiver signal-to-noise-ratio (SNR), and a 415% improvement in transceiver SNR for a particular transmission power when compared against a surface coil positioned at the same distance from the phantom, where these improvements are the maximum observed during experiments.


Subject(s)
Magnetic Resonance Imaging/instrumentation , Magnetic Resonance Imaging/methods , Algorithms , Equipment Design , Phantoms, Imaging , Signal-To-Noise Ratio
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