2010
DOI: 10.1016/j.exphem.2009.11.009
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Distinct transcriptional profiles characterize bone microenvironment mesenchymal cells rather than osteoblasts in relationship with multiple myeloma bone disease

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Cited by 59 publications
(68 citation statements)
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“…[13][14][15] Notably, these genetic differences were not found in MM patient-derived OB, 15 indicating that MSC may represent a key stromal cell population with the capacity to influence the growth of malignant MM PC. This has led investigators to examine whether MM patients show evidence of elevated MSC numbers following MM PC infiltration into the BM.…”
Section: Introductionmentioning
confidence: 99%
“…[13][14][15] Notably, these genetic differences were not found in MM patient-derived OB, 15 indicating that MSC may represent a key stromal cell population with the capacity to influence the growth of malignant MM PC. This has led investigators to examine whether MM patients show evidence of elevated MSC numbers following MM PC infiltration into the BM.…”
Section: Introductionmentioning
confidence: 99%
“…30 Although MSCs in the bone microenvironment produce OPG to prevent excess osteoclast activation, upon osteolytic tumor growth, the homeostasis shifts toward less OPG production. 44 Furthermore, because of a decreased osteogenic potential of MSCs in myeloma, [45][46][47] the osteoprogenitor cell source becomes limited to remodel bone following aggressive osteoclast damage. During this shift in balance that negatively affects OPG level, 44 supplementation of MSCs overexpressing OPG offers a dual benefit to decreasing osteoclast activation and providing additional source of osteoprogenitors.…”
Section: Discussionmentioning
confidence: 99%
“…where N H is the number of harvested cells at the end of the growth period, and N S the number of seeded cells [18].…”
Section: Methodsmentioning
confidence: 99%