Differentiation induction enhances bortezomib efficacy and overcomes drug resistance in multiple myeloma
Abstract
Aim It is of clinical importance to find methods to overcome bortezomib resistance. In the current study, we clarified the relationship between resistance to bortezomib and the differentiation status of myeloma cells, and explored the feasibility of induction of differentiation in overcoming bortezomib resistance in myeloma. Methods Cell morphology, immunoglobulin light-chain protein secretion levels, and XBP-1 expression were used to evaluate the differentiation status of myeloma cells. Low dose 2-ME2 alone or in combination with ATRA was used to induce differentiation in myeloma cells. Results The differentiation status of myeloma cells was related to myeloma sensitivity to bortezomib. After successful induction of differentiation, the myeloma cells were more sensitive to bortezomib with decreased growth and an increased rate of apoptosis. Induction of differentiation increased the proteasome workload in myeloma cells by increasing immunoglobulin secretion, while reducing proteasome capacity by decreasing proteasome activity. The imbalance between increased proteasome workload and decreased proteasome capacity is a possible mechanism by which induction of differentiation overcomes myeloma resistance to bortezomib. Conclusion The current study demonstrated, for the first time, that myeloma differentiation status is associated with myeloma sensitivity to bortezomib and that induction of differentiation can overcome myeloma resistance to bortezomib.
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Downregulation of XBP1s expression in myeloma correlates with resistance to Bortezomib.
“On the other hand, the downregulation of XBP1s expression in myeloma correlates with resistance to Bortezomib [413,414], suggesting that the comprehension of UPR effects on tumors is more complicated than we thought.”
From GANAB and N-Glycans Substrates Are Relevant in Human Physiology, Polycystic Pathology and Multiple Sclerosis: A Review (2022) · cites this paper as [413]
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“Anyway, in this topic, we have of a proteasome inhibitor, Bortezomib.”
Background
- Authors
- Gu, J.-L., Li, J., Zhou, Z.-H., Liu, J.-R., Huang, B.-H., Zheng, D., & Su, C.
- Affiliations
- Sun Yat-sen University (CN)
- Corresponding author
- Li, Juan
- Venue
- Biochemical and Biophysical Research Communications
- Publisher
- Elsevier BV
- Published
- 2012-04
- Volume
- 420
- Issue
- 3
- Pages
- 644-650
- ISSN
- 0006-291X (ISSN-L)
- OpenAlex
- W2104965094
- Cited by
- 28
- References
- 0
- Citations by year
- 2026: 1 · 2022: 1 · 2021: 3 · 2020: 1 · 2019: 2 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 1 · 2014: 5 · 2013: 6 · 2012: 1
- FWCI
- 2.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical and Biophysical Research Communications (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Multiple Myeloma Research and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
- Keywords
- bortezomib resistance, multiple myeloma, differentiation induction, proteasome inhibition, XBP1, all-trans retinoic acid, apoptosis, drug resistance reversal
- MeSH terms
- Bortezomib, Regulatory Factor X Transcription Factors, X-Box Binding Protein 1, 2-Methoxyestradiol, Antineoplastic Agents, Boronic Acids, Cell Differentiation, DNA-Binding Proteins, Estradiol, Humans, Multiple Myeloma, Pyrazines, Transcription Factors, Tretinoin, Tumor Cells, Cultured, Drug Resistance, Neoplasm
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