Details

Autor(en) / Beteiligte

• Balogh, Andrea
• Reiniger, Lilla
• Hetey, Szabolcs
• Kiraly, Peter
• Toth, Eszter
• Karaszi, Katalin
• Juhasz, Kata
• Gelencser, Zsolt
• Zvara, Agnes
• Szilagyi, Andras
• Puskas, Laszlo G
• Matko, Janos
• Papp, Zoltan
• Kovalszky, Ilona
• Juhasz, Csaba
• Than, Nandor Gabor

Titel

Decreased Expression of ZNF554 in Gliomas is Associated with the Activation of Tumor Pathways and Shorter Patient Survival

Ist Teil von

• International journal of molecular sciences, 2020-08, Vol.21 (16), p.5762

Ort / Verlag

Switzerland: MDPI

Erscheinungsjahr

2020

Quelle

MEDLINE

Beschreibungen/Notizen

• Zinc finger protein 554 (ZNF554), a member of the Krüppel-associated box domain zinc finger protein subfamily, is predominantly expressed in the brain and placenta in humans. Recently, we unveiled that ZNF554 regulates trophoblast invasion during placentation and its decreased expression leads to the early pathogenesis of preeclampsia. Since ZNF proteins are immensely implicated in the development of several tumors including malignant tumors of the brain, here we explored the pathological role of ZNF554 in gliomas. e examined the expression of ZNF554 at mRNA and protein levels in normal brain and gliomas, and then we searched for genome-wide transcriptomic changes in U87 glioblastoma cells transiently overexpressing . Immunohistochemistry of brain tissues in our cohort ( = 62) and analysis of large TCGA RNA-Seq data ( = 687) of control, oligodendroglioma, and astrocytoma tissues both revealed decreased expression of towards higher glioma grades. Furthermore, low expression was associated with shorter survival of grade III and IV astrocytoma patients. Overexpression of in U87 cells resulted in differential expression, mostly downregulation of 899 genes. The "PI3K-Akt signaling pathway", known to be activated during glioma development, was the most impacted among 116 dysregulated pathways. Most affected pathways were cancer-related and/or immune-related. Congruently, cell proliferation was decreased and cell cycle was arrested in -transfected glioma cells. These data collectively suggest that ZNF554 is a potential tumor suppressor and its decreased expression may lead to the loss of oncogene suppression, activation of tumor pathways, and shorter survival of patients with malignant glioma.