Prognosis, Biology, and Targeting of TP53 Dysregulation in Multiple Myeloma

E Flynt, K Bisht, V Sridharan, M Ortiz, F Towfic… - Cells, 2020 - mdpi.com
Multiple myeloma (MM) is the second most common hematological cancer and is
characterized by genetic features including translocations, chromosomal copy number …

Molecular and immunological mechanisms of clonal evolution in multiple myeloma

S Forster, R Radpour, AF Ochsenbein - Frontiers in immunology, 2023 - frontiersin.org
Multiple myeloma (MM) is a hematologic malignancy characterized by the proliferation of
clonal plasma cells in the bone marrow (BM). It is known that early genetic mutations in post …

Resolving therapy resistance mechanisms in multiple myeloma by multiomics subclone analysis

AM Poos, N Prokoph, MJ Przybilla, JP Mallm, S Steiger… - Blood, 2023 - ashpublications.org
Intratumor heterogeneity as a clinical challenge becomes most evident after several
treatment lines, when multidrug-resistant subclones accumulate. To address this challenge …

Functional impact of genomic complexity on the transcriptome of multiple myeloma

B Ziccheddu, MC Da Vià, M Lionetti, A Maeda… - Clinical Cancer …, 2021 - AACR
Purpose: Multiple myeloma is a biologically heterogenous plasma-cell disorder. In this
study, we aimed at dissecting the functional impact on transcriptome of gene mutations, copy …

Cytogenetic abnormalities in multiple myeloma: Incidence, prognostic significance, and geographic heterogeneity in Indian and western populations

P Kadam Amare, S Nikalje Khasnis, P Hande… - … and Genome Research, 2023 - karger.com
Multiple myeloma (MM) is a genetically complex and heterogeneous neoplasm in which
cytogenetics is a major factor playing an important role in the risk stratification of disease …

Clonal competition assays identify fitness signatures in cancer progression and resistance in multiple myeloma

L Haertle, U Munawar, HNC Hernández… - …, 2024 - Wiley Online Library
Multiple myeloma (MM) is a genetically heterogeneous disease and the management of
relapses is one of the biggest clinical challenges. TP53 alterations are established high‐risk …

Utilizing Genomics to Identify Novel Immunotherapeutic Targets in Multiple Myeloma High-Risk Subgroups

E Liu, O Jaouadi, R Sharma, N Becker, T Johnson… - bioRxiv, 2025 - biorxiv.org
Immunotherapy is now standard of care for multiple myeloma, where the most common
targets are B cell maturation antigen, CD38, and G protein-coupled receptor class C group 5 …

[HTML][HTML] Genetic alterations in members of the proteasome 26S subunit, AAA-ATPase (PSMC) gene family in the light of proteasome inhibitor resistance in multiple …

L Haertle, N Buenache, HN Cuesta Hernández… - Cancers, 2023 - mdpi.com
For the treatment of Multiple Myeloma, proteasome inhibitors are highly efficient and widely
used, but resistance is a major obstacle to successful therapy. Several underlying …

What Is Genomic High-Risk Myeloma?

FE Davies, BA Walker - Hemato, 2022 - mdpi.com
Although treatment of multiple myeloma has changed dramatically over time, there is still a
subpopulation of patients who do not respond to treatments and are labeled as high risk. A …

Modellierung Klonaler Evolution Beim Multiplen Myelom

N Müller - 2024 - search.proquest.com
In dieser Arbeit wurde ein modulares Zelllinienmodell zur Visualisierung klonaler
Evolutionsmechanismen etabliert. Hierfür wurden unterschiedlich fluoreszierende Proteine …