TY - JOUR
T1 - Allelic expression imbalance analysis identified yap1 amplification in p53-dependent osteosarcoma
AU - Niu, Guanglin
AU - Bak, Agnieszka
AU - Manyet, Melanie
AU - Zhang, Yue
AU - Pausch, Hubert
AU - Flisikowska, Tatiana
AU - Schnieke, Angelika E.
AU - Flisikowski, Krzysztof
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/3/2
Y1 - 2021/3/2
N2 - Osteosarcoma (OS) is a primary bone malignancy that mainly occurs during adolescent growth, suggesting that bone growth plays an important role in the aetiology of the disease. Genetic factors, such as heritable mutations of Rb1 and TP53, are associated with an increased risk of OS. Iden-tifying driver mutations for OS has been challenging due to the complexity of bone growth-related pathways and the extensive intra-tumoral heterogeneity of this cancer. We previously generated pigs carrying a mutated TP53 gene, which develop OS at high frequency. RNA sequencing and allele expression imbalance (AEI) analysis of OS and matched healthy control samples revealed a highly significant AEI (p = 2.14 × 10−39 ) for SNPs in the BIRC3-YAP1 locus on pig chromosome 9. Analysis of copy number variation showed that YAP1 amplification is associated with the AEI and the progression of OS. Accordingly, the inactivation of YAP1 inhibits proliferation, migration, and invasion, and leads to the silencing of TP63 and reconstruction of p16 expression in p53-deficient porcine OS cells. Increased p16 mRNA expression correlated with lower methylation of its pro-moter. Altogether, our study provides molecular evidence for the role of YAP1 amplification in the progression of p53-dependent OS.
AB - Osteosarcoma (OS) is a primary bone malignancy that mainly occurs during adolescent growth, suggesting that bone growth plays an important role in the aetiology of the disease. Genetic factors, such as heritable mutations of Rb1 and TP53, are associated with an increased risk of OS. Iden-tifying driver mutations for OS has been challenging due to the complexity of bone growth-related pathways and the extensive intra-tumoral heterogeneity of this cancer. We previously generated pigs carrying a mutated TP53 gene, which develop OS at high frequency. RNA sequencing and allele expression imbalance (AEI) analysis of OS and matched healthy control samples revealed a highly significant AEI (p = 2.14 × 10−39 ) for SNPs in the BIRC3-YAP1 locus on pig chromosome 9. Analysis of copy number variation showed that YAP1 amplification is associated with the AEI and the progression of OS. Accordingly, the inactivation of YAP1 inhibits proliferation, migration, and invasion, and leads to the silencing of TP63 and reconstruction of p16 expression in p53-deficient porcine OS cells. Increased p16 mRNA expression correlated with lower methylation of its pro-moter. Altogether, our study provides molecular evidence for the role of YAP1 amplification in the progression of p53-dependent OS.
KW - Allelic expression imbalance
KW - Bone cancer
KW - Copy number variation
KW - P16
KW - Pig
KW - TP53
KW - TP63
KW - YAP1
UR - http://www.scopus.com/inward/record.url?scp=85102649711&partnerID=8YFLogxK
U2 - 10.3390/cancers13061364
DO - 10.3390/cancers13061364
M3 - Article
AN - SCOPUS:85102649711
SN - 2072-6694
VL - 13
SP - 1
EP - 14
JO - Cancers
JF - Cancers
IS - 6
M1 - 1364
ER -