Endoplasmic reticulum chaperone prolyl 4-hydroxylase, beta polypeptide (P4HB) promotes malignant phenotypes in glioma via MAPK signaling

• Published in: Oncotarget Vol. 8; no. 42; pp. 71911 - 71923
• Main Authors: Sun, Stella, Kiang, Karrie M Y, Ho, Amy S W, Lee, Derek, Poon, Ming-Wai, Xu, Fei-Fan, Pu, Jenny K S, Kan, Amanda N C, Lee, Nikki P Y, Liu, Xiao-Bing, Man, Kwan, Day, Philip J R, Lui, Wai-Man, Fung, Ching-Fai, Leung, Gilberto K K
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 22.09.2017
• Subjects: Research Paper; glioma; P4HB; invasion; angiogenesis; MAPK signaling
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.18026

Endoplasmic reticulum (ER) chaperone Prolyl 4-hydroxylase, beta polypeptide (P4HB) has previously been identified as a novel target for chemoresistance in glioblastoma multiforme (GBM). Yet its functional roles in glioma carcinogenesis remain elusive. In clinical analysis using human glioma specimens and Gene Expression Omnibus (GEO) profiles, we found that aberrant expression of P4HB was correlated with high-grade malignancy and an angiogenic phenotype in glioma. Furthermore, P4HB upregulation conferred malignant characteristics including proliferation, invasion, migration and angiogenesis , and increased tumor growth via the mitogen-activated protein kinase (MAPK) signaling pathway. Pathway analysis suggested genetic and pharmacologic inhibition of P4HB suppressed MAPK expression and its downstream targets were involved in angiogenesis and invasion. This is the first study that demonstrates the oncogenic roles of P4HB and its underlying mechanism in glioma. Since tumor invasion and Vascularisation are typical hallmarks in malignant glioma, our findings uncover a promising anti-glioma mechanism through P4HB-mediated retardation of MAPK signal transduction.