MAOB expression correlates with a favourable prognosis in prostate cancer, and its genetic variants are associated with the metastasis of the disease

• Published in: Journal of cellular and molecular medicine Vol. 28; no. 8; pp. e18229 - n/a
• Main Authors: Huang, Hsiang‐Ching, Hsieh, Yi‐Hsien, Hsiao, Chi‐Hao, Lin, Chia‐Yen, Wang, Shian‐Shiang, Ho, Kuo‐Hao, Chang, Lun‐Ching, Huang, Huei‐Mei, Yang, Shun‐Fa, Chien, Ming‐Hsien
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.04.2024; John Wiley and Sons Inc
• Subjects: Alleles; Amine oxidase (flavin-containing); Androgens; Biopsy; Biotechnology; Cancer therapies; Cell proliferation; Cholangiocarcinoma; clinicopathologic development; Disease; Genes; Genetic diversity; Genomes; Genotype; Humans; Kinases; Liver cancer; Lymph nodes; Lymphatic system; Male; Medical prognosis; Metastases; Metastasis; Monoamine Oxidase; monoamine oxidase B; Original; Polymorphism, Single Nucleotide - genetics; Prognosis; Prostate cancer; Prostate-specific antigen; Prostatic Neoplasms - genetics; Proteins; Single-nucleotide polymorphism; United States > US; Taiwan; prostate cancer; single‐nucleotide polymorphism; monoamine oxidase B; prognosis; clinicopathologic development
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/jcmm.18229

Monoamine oxidase B (MAOB), a neurotransmitter‐degrading enzyme, was reported to reveal conflicting roles in various cancers. However, the functional role of MAOB and impacts of its genetic variants on prostate cancer (PCa) is unknown. Herein, we genotyped four loci of MAOB single‐nucleotide polymorphisms (SNPs), including rs1799836 (A/G), rs3027452 (G/A), rs6651806 (A/C) and rs6324 (G/A) in 702 PCa Taiwanese patients. We discovered that PCa patients carrying the MAOB rs6324 A‐allele exhibited an increased risk of having a high initial prostate‐specific antigen (iPSA) level (>10 ng/mL). Additionally, patients with the rs3027452 A‐allele had a higher risk of developing distal metastasis, particularly in the subpopulation with high iPSA levels. In a subpopulation without postoperative biochemical recurrence, patients carrying the rs1799836 G‐allele had a higher risk of developing lymph node metastasis and recurrence compared to those carrying the A‐allele. Furthermore, genotype screening in PCa cell lines revealed that cells carrying the rs1799836 G‐allele expressed lower MAOB levels than those carrying the A‐allele. Functionally, overexpression and knockdown of MAOB in PCa cells respectively suppressed and enhanced cell motility and proliferation. In clinical observations, correlations of lower MAOB expression levels with higher Gleason scores, advanced clinical T stages, tumour metastasis, and poorer prognosis in PCa patients were noted. Our findings suggest that MAOB may act as a suppressor of PCa progression, and the rs3027452 and rs1799836 genetic variants of MAOB are linked to PCa metastasis within the Taiwanese population.