2020
DOI: 10.1111/cas.14644
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Epigenetic inactivation of IRX4 is responsible for acceleration of cell growth in human pancreatic cancer

Abstract: Epigenetic gene silencing by aberrant DNA methylation is one of the important mechanisms leading to loss of key cellular pathways in tumorigenesis. Methyl‐CpG‐targeted transcriptional activation (MeTA) reactivates hypermethylation‐mediated silenced genes in a different way from DNA‐demethylating agents. Microarray coupled with MeTA (MeTA‐array) identified seven commonly hypermethylation‐mediated silenced genes in 12 pancreatic ductal adenocarcinoma (PDAC) cell lines. Among these, we focused on IRX4 (Iroquois h… Show more

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Cited by 5 publications
(2 citation statements)
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“…It was also observed that the promoter region of IRX4 was frequently and specifically hypermethylated in pancreatic primary tumors. Moreover, the re-expression of IRX4 in pancreatic cancer cell lines was able to inhibit colony formation and cell proliferation [ 69 ].…”
Section: Iroquois Family Genes In Cancermentioning
confidence: 99%
“…It was also observed that the promoter region of IRX4 was frequently and specifically hypermethylated in pancreatic primary tumors. Moreover, the re-expression of IRX4 in pancreatic cancer cell lines was able to inhibit colony formation and cell proliferation [ 69 ].…”
Section: Iroquois Family Genes In Cancermentioning
confidence: 99%
“…Promotion of IRX3 signaling or inhibition of IRX5 signaling may be a pathway for differentiation therapy in nephroblastoma (11). Epigenetic inactivation of IRX4 accelerates the growth of human pancreatic cancer cells (12). IRX5 plays an important role in VSMC G1/S phase cell cycle checkpoint control and apoptosis (13).…”
Section: Introductionmentioning
confidence: 99%