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Nicotinamide N-methyltransferase (NNMT) catalyzes the methylation of nicotinamide. Our previous works indicate that NNMT is involved in the body mass index and energy metabolism, and recently the association between a SNP (rs694539) of and a variety of cardiovascular diseases was reported. At present, more than 200 single nucleotide polymorphisms (SNPs) have been identified in the databases of the human genome projects; however, the association between rs694539 variation and hyperlipidemia has not been reported yet, and whether there are any SNPs in significantly associated with hyperlipidemia is still unclear. In this paper, we selected 19 SNPs in as the tagSNPs using Haploview software (Haploview 4.2) first and then performed a case-control study to observe the association between these tagSNPs and hyperlipidemia and finally applied physiological approaches to explore the possible mechanisms through which the polymorphism induces hyperlipidemia. The results show that a SNP (rs1941404) in is significantly associated with hyperlipidemia, and the influence of rs1941404 variation on the resting energy expenditure may be the possible mechanism for rs1941404 variation to induce hyperlipidemia.
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http://dx.doi.org/10.1155/2016/7521942 | DOI Listing |
Hum Cell
August 2025
Department of Obstetrics and Gynecology, Teikyo University School of Medicine, 11-1 Kaga, Itabashi-Ku, Tokyo, Japan.
Nicotinamide N-methyltransferase (NNMT) is an S-adenosyl-l-methionine (SAM)-dependent cytosolic enzyme, and a growing body of evidence suggest that it plays an essential role in cancer progression. Recently, NNMT has a role in methylation metabolism and tumorigenesis and was associated with a poor prognosis against numerous cancers. In addition, it has been reported that NNMT has been overexpressed in the stroma of advanced high-grade serous carcinoma and may contribute to decreased survival.
View Article and Find Full Text PDFArch Biochem Biophys
August 2025
Department of Plastic Surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Keloid are characterized by fibroblastic proliferation and excessive collagen deposition. Nicotinamide N-methyltransferase (NNMT) belongs to the methyltransferase family and plays an important role in various physiological processes, including keloid formation. However, the role of NNMT in keloid development remains poorly understood.
View Article and Find Full Text PDFArch Biochem Biophys
October 2025
Physical Education College, Jiangxi Normal University, Nanchang, 330022, Jiangxi Province, China. Electronic address:
Non-alcoholic fatty liver disease (NAFLD), characterized by abnormal lipid accumulation in hepatocytes, is a prevalent metabolic disorder strongly linked to insulin resistance and obesity. Emerging evidence highlights the central role of nicotinamide N-methyltransferase (NNMT) in NAFLD pathogenesis through its regulation of nicotinamide adenine dinucleotide (NAD) metabolism, the methionine cycle, epigenetic modifications, and gut microbiota. NNMT methylates NAM to methylnicotinamide (MNAM), consuming SAM, raising SAH/Hcy, depleting NAD and worsening oxidative stress.
View Article and Find Full Text PDFNature
July 2025
Department of Obstetrics and Gynecology, Section of Gynecologic Oncology, University of Chicago, Chicago, IL, USA.
Cancer-associated fibroblasts (CAFs) have a pivotal cancer-supportive role, yet CAF-targeted therapies are lacking. Here, using spatial transcriptomics and single-cell RNA sequencing, we investigate the role of nicotinamide N-methyltransferase (NNMT) in high-grade serous ovarian cancer. Mechanistically, NNMT-induced H3K27me3 hypomethylation drives complement secretion from CAFs, attracting immunosuppressive myeloid-derived suppressor cells (MDSCs) to the tumour.
View Article and Find Full Text PDFGut
August 2025
State Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, Jinan University, Guangzhou, Guangdong, China minfengche
Background: Circulating tumour cell (CTC)-neutrophil clusters represent a key driver and a hallmark of tumour metastasis; however, efficient approaches for their elimination are still lacking.
Objective: This study sought to elucidate the location and mechanisms of CTC-neutrophil cluster formation and develop more effective antimetastasis strategies.
Design: Immunofluorescence staining of clinical colorectal cancer (CRC) samples was performed to identify the location of CTC-neutrophil clusters.