» Articles » PMID: 33570672

Morphogens and Growth Factor Signalling in the Myeloma Bone-lining Niche

Overview
Publisher Springer
Specialty Biology
Date 2021 Feb 11
PMID 33570672
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Multiple myeloma is a malignancy caused by the clonal expansion of abnormal plasma cells. Myeloma cells have proven to be incredibly successful at manipulating their microenvironment to promote growth and to evade modern therapies. They have evolved to utilise the integral signalling pathways of the bone and bone marrow to drive disease progression. The bone marrow is often described in the context of a single structure that fills the bone cavity and supports normal haematopoiesis. However, within that structure exists two anatomically different niches, the perivascular niche and the endosteal niche. These contain different cell types functioning to support normal immune and blood cell production as well as healthy bone. These cells secrete numerous signalling molecules that can influence myeloma cell biology and behaviour. The endosteal niche is home to specific bone cell lineages and plays a pivotal role in myeloma cell establishment and survival. This review will concentrate on some of the signalling pathways that are hijacked by myeloma cells to shape a favourable environment, and the different influences myeloma cells are exposed to depending on their spatial location within the bone marrow.

Citing Articles

Mitochondria-associated programmed cell death: elucidating prognostic biomarkers, immune checkpoints, and therapeutic avenues in multiple myeloma.

Gao G, Miao J, Jia Y, He A Front Immunol. 2024; 15:1448764.

PMID: 39726602 PMC: 11670199. DOI: 10.3389/fimmu.2024.1448764.


A comprehensive review of oncogenic Notch signaling in multiple myeloma.

Roosma J PeerJ. 2024; 12:e18485.

PMID: 39619207 PMC: 11608568. DOI: 10.7717/peerj.18485.


Advances in hematopoietic stem cells ex vivo expansion associated with bone marrow niche.

Deng J, Tan Y, Xu Z, Wang H Ann Hematol. 2024; 103(12):5035-5057.

PMID: 38684510 DOI: 10.1007/s00277-024-05773-1.


Emerging roles of growth factors in osteonecrosis of the femoral head.

Che Z, Song Y, Zhu L, Liu T, Li X, Huang L Front Genet. 2022; 13:1037190.

PMID: 36452155 PMC: 9702520. DOI: 10.3389/fgene.2022.1037190.


The role of the bone microenvironment in regulating myeloma residual disease and treatment.

Dadzie T, Green A Front Oncol. 2022; 12:999939.

PMID: 36072809 PMC: 9441696. DOI: 10.3389/fonc.2022.999939.


References
1.
Silbermann R, Roodman G . Current Controversies in the Management of Myeloma Bone Disease. J Cell Physiol. 2016; 231(11):2374-9. DOI: 10.1002/jcp.25351. View

2.
Walker B, Wardell C, Murison A, Boyle E, Begum D, Dahir N . APOBEC family mutational signatures are associated with poor prognosis translocations in multiple myeloma. Nat Commun. 2015; 6:6997. PMC: 4568299. DOI: 10.1038/ncomms7997. View

3.
Manier S, Salem K, Park J, Landau D, Getz G, Ghobrial I . Genomic complexity of multiple myeloma and its clinical implications. Nat Rev Clin Oncol. 2016; 14(2):100-113. DOI: 10.1038/nrclinonc.2016.122. View

4.
Bergsagel P, Kuehl W, Zhan F, Sawyer J, Barlogie B, Shaughnessy Jr J . Cyclin D dysregulation: an early and unifying pathogenic event in multiple myeloma. Blood. 2005; 106(1):296-303. PMC: 1895118. DOI: 10.1182/blood-2005-01-0034. View

5.
Prideaux S, Conway OBrien E, Chevassut T . The genetic architecture of multiple myeloma. Adv Hematol. 2014; 2014:864058. PMC: 3996928. DOI: 10.1155/2014/864058. View