TY - JOUR
T1 - p53 maintains baseline expression of multiple tumor suppressor genes
AU - Pappas, Kyrie
AU - Xu, Jia
AU - Zairis, Sakellarios
AU - Resnick-Silverman, Lois
AU - Abate, Francesco
AU - Steinbach, Nicole
AU - Ozturk, Sait
AU - Saal, Lao H.
AU - Su, Tao
AU - Cheung, Pamela
AU - Schmidt, Hank
AU - Aaronson, Stuart
AU - Hibshoosh, Hanina
AU - Manfredi, James
AU - Rabadan, Raul
AU - Parsons, Ramon
PY - 2017/8/1
Y1 - 2017/8/1
N2 - TP53 is the most commonly mutated tumor suppressor gene and its mutation drives tumorigenesis. Using ChIP-seq for p53 in the absence of acute cell stress, we found that wild-type but not mutant p53 binds and activates numerous tumor suppressor genes, including PTEN, STK11(LKB1), miR-34a, KDM6A(UTX), FOXO1, PHLDA3, and TNFRSF10B through consensus binding sites in enhancers and promoters. Depletion of p53 reduced expression of these target genes, and analysis across 18 tumor types showed that mutation of TP53 associated with reduced expression of many of these genes. Regarding PTEN, p53 activated expression of a luciferase reporter gene containing the p53-consensus site in the PTEN enhancer, and homozygous deletion of this region in cells decreased PTEN expression and increased growth and transformation. These findings show that p53 maintains expression of a team of tumor suppressor genes that may together with the stress-induced targets mediate the ability of p53 to suppress cancer development. p53 mutations selected during tumor initiation and progression, thus, inactivate multiple tumor suppressor genes in parallel, which could account for the high frequency of p53 mutations in cancer.
AB - TP53 is the most commonly mutated tumor suppressor gene and its mutation drives tumorigenesis. Using ChIP-seq for p53 in the absence of acute cell stress, we found that wild-type but not mutant p53 binds and activates numerous tumor suppressor genes, including PTEN, STK11(LKB1), miR-34a, KDM6A(UTX), FOXO1, PHLDA3, and TNFRSF10B through consensus binding sites in enhancers and promoters. Depletion of p53 reduced expression of these target genes, and analysis across 18 tumor types showed that mutation of TP53 associated with reduced expression of many of these genes. Regarding PTEN, p53 activated expression of a luciferase reporter gene containing the p53-consensus site in the PTEN enhancer, and homozygous deletion of this region in cells decreased PTEN expression and increased growth and transformation. These findings show that p53 maintains expression of a team of tumor suppressor genes that may together with the stress-induced targets mediate the ability of p53 to suppress cancer development. p53 mutations selected during tumor initiation and progression, thus, inactivate multiple tumor suppressor genes in parallel, which could account for the high frequency of p53 mutations in cancer.
UR - http://www.scopus.com/inward/record.url?scp=85026624819&partnerID=8YFLogxK
U2 - 10.1158/1541-7786.MCR-17-0089
DO - 10.1158/1541-7786.MCR-17-0089
M3 - Article
C2 - 28483946
AN - SCOPUS:85026624819
SN - 1541-7786
VL - 15
SP - 1051
EP - 1062
JO - Molecular Cancer Research
JF - Molecular Cancer Research
IS - 8
ER -