Age-related mesenchymal stromal cell senescence is associated with progression from MGUS to multiple myeloma

The risk of progression of monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) increases with advancing age, suggesting that progression may be influenced by age-related changes within the bone marrow (BM) microenvironment. We hypothesise that senescent mesenchymal stromal cells (MSCs), which accumulate in the BM with age, may contribute to MGUS progression to MM. Here, we show that, like BM MSCs from aged non-cancer controls, BM MSCs from both MM and MGUS patients exhibit a senescent phenotype characterised by enlarged, flattened morphology, increased β-galactosidase activity and CDKN2A expression, and decreased proliferation rate compared with BM MSCs from healthy young individuals. While coculture with BM MSCs suppresses the proliferative capacity of MM cell lines in vitro, induction of senescence via irradiation or replicative exhaustion in healthy MSCs relieves this suppression, compared with non-senescent MSCs. This may, in part, be attributable to upregulated expression of the BMP antagonist Gremlin1 in senescent MSCs, which facillitates MM cell proliferation. Notably, the risk of progression to MM was significantly elevated in MGUS patients with increased MSC senescence. Collectively, our data provide evidence that age-related accumulation of senescent MSCs may be a driver of MGUS to MM progression.

Authors

Institutions

Publication Details

Journal
Leukemia
Published
2025-04-22
DOI
https://doi.org/10.1038/s41375-025-02621-7
Citations
5
Primary Topic
Multiple Myeloma Research and Treatments
Type
article
Field-Weighted Citation Impact
8.85

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Age-related mesenchymal stromal cell senescence is associated with progression from MGUS to multiple myeloma

Vasilios Panagopoulos, Andrew C.W. Zannettino, Melissa Cantley, Cindy Lee et al.
5 citations
Leukemia
Multiple Myeloma Research and Treatments
8.85
article

Age-related mesenchymal stromal cell senescence is associated with progression from MGUS to multiple myeloma

Vasilios Panagopoulos, Andrew C.W. Zannettino, Melissa Cantley, Cindy Lee, Peter I. Croucher, Sheila A. Stewart, Krzysztof M. Mrozik, Angelina Yong, Kimberley C. Clark, Dimitrios Cakouros, Noemi Horvath, D. Hewett, Kate Vandyke, Stan Gronthos, Natalya Plakhova, Laura J. Trainor, J. Gardiner
article en
5 citations

Abstract

The risk of progression of monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) increases with advancing age, suggesting that progression may be influenced by age-related changes within the bone marrow (BM) microenvironment. We hypothesise that senescent mesenchymal stromal cells (MSCs), which accumulate in the BM with age, may contribute to MGUS progression to MM. Here, we show that, like BM MSCs from aged non-cancer controls, BM MSCs from both MM and MGUS patients exhibit a senescent phenotype characterised by enlarged, flattened morphology, increased β-galactosidase activity and CDKN2A expression, and decreased proliferation rate compared with BM MSCs from healthy young individuals. While coculture with BM MSCs suppresses the proliferative capacity of MM cell lines in vitro, induction of senescence via irradiation or replicative exhaustion in healthy MSCs relieves this suppression, compared with non-senescent MSCs. This may, in part, be attributable to upregulated expression of the BMP antagonist Gremlin1 in senescent MSCs, which facillitates MM cell proliferation. Notably, the risk of progression to MM was significantly elevated in MGUS patients with increased MSC senescence. Collectively, our data provide evidence that age-related accumulation of senescent MSCs may be a driver of MGUS to MM progression.

LeukemiaVol. 39(6)
Royal Adelaide Hospital (AU), Garvan Institute of Medical Research (AU), Washington University in St. Louis (US), South Australian Health and Medical Research Institute (AU), The University of Adelaide (AU)
Foundation for Barnes-Jewish Hospital, Ernest Heine Family Foundation, Hospital Research Foundation, South Australian Health and Medical Research Institute, Government of South Australia, Cancer Australia, University of Adelaide, Royal Adelaide Hospital, National Institutes of Health, Medical Research Council, National Health and Medical Research Council, Cancer Council South Australia, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 2%
Multiple Myeloma Research and Treatments
8.85
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.