| Literature DB >> 33619369 |
Yael C Cohen1,2, Mor Zada1,3, Shuang-Yin Wang3, Chamutal Bornstein3, Eyal David3, Adi Moshe3, Baoguo Li3, Shir Shlomi-Loubaton3, Moshe E Gatt4, Chamutal Gur3,4, Noa Lavi5, Chezi Ganzel6, Efrat Luttwak1,2, Evgeni Chubar7, Ory Rouvio8, Iuliana Vaxman1,9, Oren Pasvolsky1,9, Mouna Ballan10, Tamar Tadmor11, Anatoly Nemets12, Osnat Jarchowcky-Dolberg13, Olga Shvetz14, Meirav Laiba15, Ofer Shpilberg16, Najib Dally17, Irit Avivi1,2, Assaf Weiner18, Ido Amit19.
Abstract
Multiple myeloma (MM) is a neoplastic plasma-cell disorder characterized by clonal proliferation of malignant plasma cells. Despite extensive research, disease heterogeneity within and between treatment-resistant patients is poorly characterized. In the present study, we conduct a prospective, multicenter, single-arm clinical trial (NCT04065789), combined with longitudinal single-cell RNA-sequencing (scRNA-seq) to study the molecular dynamics of MM resistance mechanisms. Newly diagnosed MM patients (41), who either failed to respond or experienced early relapse after a bortezomib-containing induction regimen, were enrolled to evaluate the safety and efficacy of a daratumumab, carfilzomib, lenalidomide and dexamethasone combination. The primary clinical endpoint was safety and tolerability. Secondary endpoints included overall response rate, progression-free survival and overall survival. Treatment was safe and well tolerated; deep and durable responses were achieved. In prespecified exploratory analyses, comparison of 41 primary refractory and early relapsed patients, with 11 healthy subjects and 15 newly diagnosed MM patients, revealed new MM molecular pathways of resistance, including hypoxia tolerance, protein folding and mitochondria respiration, which generalized to larger clinical cohorts (CoMMpass). We found peptidylprolyl isomerase A (PPIA), a central enzyme in the protein-folding response pathway, as a potential new target for resistant MM. CRISPR-Cas9 deletion of PPIA or inhibition of PPIA with a small molecule inhibitor (ciclosporin) significantly sensitizes MM tumor cells to proteasome inhibitors. Together, our study defines a roadmap for integrating scRNA-seq in clinical trials, identifies a signature of highly resistant MM patients and discovers PPIA as a potent therapeutic target for these tumors.Entities:
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Year: 2021 PMID: 33619369 PMCID: PMC7612793 DOI: 10.1038/s41591-021-01232-w
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 87.241