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PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors
by
Djekidel, Nadhir
, Reed, Kristin B.
, Adkins, Grace E.
, Hatley, Mark E.
, Xu, Beisi
, Jin, Hongjian
, Pruett-Miller, Shondra M.
, Schreiner, Patrick A.
, Langdon, Casey G.
, Vuong, Kyna
, Abraham, Brian J.
, Porter, Shaina N.
, Zhang, Yang
, Stevens, Bradley T.
, Kimbrough, Darden W.
, Gadek, Katherine E.
, Searcy, Madeline B.
, Garcia, Matthew R.
, Drummond, Catherine J.
, Rehg, Jerold E.
, Larsen, Randolph K.
in
13/1
/ 13/100
/ 13/106
/ 13/109
/ 13/31
/ 13/51
/ 13/89
/ 38/35
/ 38/39
/ 38/77
/ 38/90
/ 38/91
/ 59/57
/ 631/532/2435
/ 631/67/1798
/ 631/67/2332
/ 64/110
/ 64/60
/ 82/1
/ Animal models
/ Cell differentiation
/ Endothelial cells
/ FOXO1 protein
/ Humanities and Social Sciences
/ multidisciplinary
/ Muscles
/ Pax3 protein
/ Pediatrics
/ Progenitor cells
/ Rhabdomyosarcoma
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Stem cells
2023
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PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors
by
Djekidel, Nadhir
, Reed, Kristin B.
, Adkins, Grace E.
, Hatley, Mark E.
, Xu, Beisi
, Jin, Hongjian
, Pruett-Miller, Shondra M.
, Schreiner, Patrick A.
, Langdon, Casey G.
, Vuong, Kyna
, Abraham, Brian J.
, Porter, Shaina N.
, Zhang, Yang
, Stevens, Bradley T.
, Kimbrough, Darden W.
, Gadek, Katherine E.
, Searcy, Madeline B.
, Garcia, Matthew R.
, Drummond, Catherine J.
, Rehg, Jerold E.
, Larsen, Randolph K.
in
13/1
/ 13/100
/ 13/106
/ 13/109
/ 13/31
/ 13/51
/ 13/89
/ 38/35
/ 38/39
/ 38/77
/ 38/90
/ 38/91
/ 59/57
/ 631/532/2435
/ 631/67/1798
/ 631/67/2332
/ 64/110
/ 64/60
/ 82/1
/ Animal models
/ Cell differentiation
/ Endothelial cells
/ FOXO1 protein
/ Humanities and Social Sciences
/ multidisciplinary
/ Muscles
/ Pax3 protein
/ Pediatrics
/ Progenitor cells
/ Rhabdomyosarcoma
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Stem cells
2023
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PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors
by
Djekidel, Nadhir
, Reed, Kristin B.
, Adkins, Grace E.
, Hatley, Mark E.
, Xu, Beisi
, Jin, Hongjian
, Pruett-Miller, Shondra M.
, Schreiner, Patrick A.
, Langdon, Casey G.
, Vuong, Kyna
, Abraham, Brian J.
, Porter, Shaina N.
, Zhang, Yang
, Stevens, Bradley T.
, Kimbrough, Darden W.
, Gadek, Katherine E.
, Searcy, Madeline B.
, Garcia, Matthew R.
, Drummond, Catherine J.
, Rehg, Jerold E.
, Larsen, Randolph K.
in
13/1
/ 13/100
/ 13/106
/ 13/109
/ 13/31
/ 13/51
/ 13/89
/ 38/35
/ 38/39
/ 38/77
/ 38/90
/ 38/91
/ 59/57
/ 631/532/2435
/ 631/67/1798
/ 631/67/2332
/ 64/110
/ 64/60
/ 82/1
/ Animal models
/ Cell differentiation
/ Endothelial cells
/ FOXO1 protein
/ Humanities and Social Sciences
/ multidisciplinary
/ Muscles
/ Pax3 protein
/ Pediatrics
/ Progenitor cells
/ Rhabdomyosarcoma
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Stem cells
2023
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PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors
Journal Article
PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors
2023
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Overview
Fusion-positive rhabdomyosarcoma (FP-RMS) driven by the expression of the PAX3-FOXO1 (P3F) fusion oncoprotein is an aggressive subtype of pediatric rhabdomyosarcoma. FP-RMS histologically resembles developing muscle yet occurs throughout the body in areas devoid of skeletal muscle highlighting that FP-RMS is not derived from an exclusively myogenic cell of origin. Here we demonstrate that P3F reprograms mouse and human endothelial progenitors to FP-RMS. We show that P3F expression in
aP2-Cre
expressing cells reprograms endothelial progenitors to functional myogenic stem cells capable of regenerating injured muscle fibers. Further, we describe a FP-RMS mouse model driven by P3F expression and
Cdkn2a
loss in endothelial cells. Additionally, we show that P3F expression in
TP53
-null human iPSCs blocks endothelial-directed differentiation and guides cells to become myogenic cells that form FP-RMS tumors in immunocompromised mice. Together these findings demonstrate that FP-RMS can originate from aberrant development of non-myogenic cells driven by P3F.
Histologically, PAX3-FOXO1 (P3F) fusion-positive rhabdomyosarcoma (FP-RMS) resembles muscles cells, however, its cell-of-origin is less clear. Here, the authors demonstrate that P3F expression induces endothelial cells reprogramming into functional myogenic stem cells, driving the formation of FP-RMS in mouse models.
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