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Updated: Nov 7, 2025

Repression of Multiple Myeloma Cell Growth In Vivo by Single-wall Carbon Nanotube SWCNT-delivered MALAT1 Antisense Oligos
Published on: December 13, 2018
Targeted Therapies for Multiple Myeloma
Christopher Chang-Yew Leow1, Michael Sze Yuan Low1
1Monash Haematology, 246 Clayton Road, Clayton, VIC 3168, Australia.
Abstract:
Multiple myeloma continues to be a challenging disorder to treat despite improved therapies and the widespread use of proteasome inhibitors and immunomodulatory drugs. Although patient outcomes have improved, the disease continues to invariably relapse, and in the majority of cases, a cure remains elusive. In the last decade, there has been an explosion of novel drugs targeting cellular proteins essential for malignant plasma cell proliferation and survival. In this review, we focus on novel druggable targets leading to the development of monoclonal antibodies and cellular therapies against surface antigens (CD38, CD47, CD138, BCMA, SLAMF7, GPRC5D, FcRH5), inhibitors of epigenetic regulators such as histone deacetylase (HDAC), and agents targeting anti-apoptotic (BCL-2), ribosomal (eEF1A2) and nuclear export (XPO1) proteins.
Insights
Novel therapies are emerging for multiple myeloma, a challenging blood cancer. This review highlights new drugs targeting surface antigens, epigenetic regulators, and proteins involved in cell survival and proliferation.
Area of Science:
- Hematology
- Oncology
- Pharmacology
Background:
- Multiple myeloma remains a difficult-to-treat blood cancer, often relapsing despite current therapies like proteasome inhibitors and immunomodulatory drugs.
- Significant advancements have improved patient outcomes, yet a definitive cure for multiple myeloma is still elusive.
- The development of novel therapeutic strategies is crucial for overcoming treatment resistance and improving long-term survival.
Purpose of the Study:
- To review novel druggable targets and emerging therapies for multiple myeloma.
- To provide an overview of new therapeutic agents targeting specific proteins and pathways crucial for myeloma cell survival and proliferation.
- To highlight the potential of monoclonal antibodies, cellular therapies, and small molecule inhibitors in treating relapsed or refractory multiple myeloma.
Main Methods:
- Literature review of recent research on novel drug targets and therapies for multiple myeloma.
- Analysis of emerging therapeutic classes including monoclonal antibodies, cellular therapies, and small molecule inhibitors.
- Categorization of novel targets based on their cellular function, such as surface antigens, epigenetic regulators, and anti-apoptotic proteins.
Main Results:
- Identification of multiple novel surface antigens (e.g., CD38, BCMA, GPRC5D) targeted by monoclonal antibodies and cellular therapies.
- Exploration of inhibitors targeting epigenetic regulators like histone deacetylase (HDAC) for multiple myeloma treatment.
- Discussion of agents targeting essential proteins such as BCL-2, eEF1A2, and XPO1 to induce apoptosis and overcome resistance.
Conclusions:
- Emerging therapies targeting novel molecular pathways offer promising new avenues for treating multiple myeloma.
- Monoclonal antibodies and cellular therapies against specific surface antigens represent a significant advancement in myeloma treatment.
- Targeting epigenetic regulators and anti-apoptotic proteins provides alternative strategies for overcoming drug resistance and improving patient outcomes in multiple myeloma.
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