Table 1.

Genes and processes recently revealed to have roles in both HSC aging and transformation

GeneExpression in old vs young HSCsHSC phenotypeHematologic malignancy phenotypeFunction
Selp HSC aging (RNA and protein38Knockout increases hematopoietic regeneration39  Knockout accelerates leukemogenesis in CML39,40  Cell adhesion molecule produced by platelets and endothelial cells for leukocyte adhesion38  
Nupr1 HSC aging (RNA38Knockout increases HSC quiescence and engraftment potency41  Targeted inhibition reduces the growth of AML, T-cell ALL, lymphoma, and multiple myeloma cell lines42,43  High-mobility group protein family member involved in apoptosis, stress response, and cancer progression41  
Sema4a HSC aging (RNA38Knockout increases myeloid-biased HSC proliferation and impairs regenerative capacity44  Knockout impairs multiple myeloma cell growth45  Binds to surface receptor Plexin-D1, essential for HSC self-renewal and protection from stress44  
Cited2 HSC aging (RNA38Knockout depletes functional HSCs in young mice46  Knockdown decreases AML pathogenesis and induces apoptosis47  Binding partner of the acetyltransferase CBP/p300 in transcriptional regulation46  
Hsf1 HSC aging (protein48Dispensable in young HSCs; knockout impairs hematopoietic regeneration by middle age48  Knockout impairs initiation and maintenance of AML and T-cell ALL49,50  Maintains proteostasis and self-renewal in response to stress48  
Igf2bp2 HSC aging (RNA51Knockout impairs HSC function in young mice51  Knockdown inhibits the growth of AML cell lines52  RNA-binding protein that regulates messenger RNA stability and translation51  
Egr1 HSC aging (RNA53Knockout increases HSC cycling and mobilization54  Tumor suppressor in ALL, CML, and AML55  Transcription factor that regulates cell growth, differentiation, and depolarization55  
Twist1 HSC aging (RNA56Knockout reduces HSC self-renewal and causes myeloid-biased hematopoiesis56  Knockdown reduces AML cell line proliferation and sensitizes to decitabine57  Transcription factor essential for embryonic mesoderm development56  
Gata2 No change (RNA38Haploinsufficiency promotes HSC proliferation and functional decline58  Haploinsufficiency causes long latency but aggressive MDS and AML59  Essential transcription factor for fetal and adult hematopoiesis60  
GeneExpression in old vs young HSCsHSC phenotypeHematologic malignancy phenotypeFunction
Selp HSC aging (RNA and protein38Knockout increases hematopoietic regeneration39  Knockout accelerates leukemogenesis in CML39,40  Cell adhesion molecule produced by platelets and endothelial cells for leukocyte adhesion38  
Nupr1 HSC aging (RNA38Knockout increases HSC quiescence and engraftment potency41  Targeted inhibition reduces the growth of AML, T-cell ALL, lymphoma, and multiple myeloma cell lines42,43  High-mobility group protein family member involved in apoptosis, stress response, and cancer progression41  
Sema4a HSC aging (RNA38Knockout increases myeloid-biased HSC proliferation and impairs regenerative capacity44  Knockout impairs multiple myeloma cell growth45  Binds to surface receptor Plexin-D1, essential for HSC self-renewal and protection from stress44  
Cited2 HSC aging (RNA38Knockout depletes functional HSCs in young mice46  Knockdown decreases AML pathogenesis and induces apoptosis47  Binding partner of the acetyltransferase CBP/p300 in transcriptional regulation46  
Hsf1 HSC aging (protein48Dispensable in young HSCs; knockout impairs hematopoietic regeneration by middle age48  Knockout impairs initiation and maintenance of AML and T-cell ALL49,50  Maintains proteostasis and self-renewal in response to stress48  
Igf2bp2 HSC aging (RNA51Knockout impairs HSC function in young mice51  Knockdown inhibits the growth of AML cell lines52  RNA-binding protein that regulates messenger RNA stability and translation51  
Egr1 HSC aging (RNA53Knockout increases HSC cycling and mobilization54  Tumor suppressor in ALL, CML, and AML55  Transcription factor that regulates cell growth, differentiation, and depolarization55  
Twist1 HSC aging (RNA56Knockout reduces HSC self-renewal and causes myeloid-biased hematopoiesis56  Knockdown reduces AML cell line proliferation and sensitizes to decitabine57  Transcription factor essential for embryonic mesoderm development56  
Gata2 No change (RNA38Haploinsufficiency promotes HSC proliferation and functional decline58  Haploinsufficiency causes long latency but aggressive MDS and AML59  Essential transcription factor for fetal and adult hematopoiesis60  
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