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Neuroblastoma (NB), a common infantile neuroendocrine tumor, presents a substantial therapeutic challenge when MYCN is amplified. Given that the protein structure of N-Myc is disordered, we utilized Alphafold for prediction and GROMACS for optimization of the N-Myc structure, thereby improving the reliability of the predicted structure. The publicly available datasets GSE49710 and GSE73517 were adopted, which contain the transcriptome data of clinical samples from 598 NB patients. Through various machine learning algorithms, FAM13A was identified as a characteristic gene of MYCN. Cell functional experiments, including those on cell proliferation, apoptosis, and cell cycle, also indicate that FAM13A is a potential risk factor. Additionally, Alphafold and GROMACS were employed to predict and optimize the structure of FAM13A. Protein-protein docking and molecular dynamic modeling techniques were then used to validate the enhanced protein stability resulting from the interaction between N-Myc and FAM13A. Consequently, targeting FAM13A holds the potential to reduce the stability of N-Myc, hinder the proliferation of NB cells, and increase the infiltration of immune cells. This multi-faceted approach effectively combats tumor cells, making FAM13A a prospective therapeutic target for MYCN-amplified NB.
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http://dx.doi.org/10.1186/s12885-025-13903-9 | DOI Listing |
J Int Med Res
September 2025
Department of Physiology, Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Vietnam.
ObjectivesGenome-wide association studies have identified as a gene linked to chronic obstructive pulmonary disease. Several single-nucleotide polymorphisms-notably, rs7671167, rs2869967, rs2869966, and rs17014601-are associated with chronic obstructive pulmonary disease susceptibility and spirometric indices. This study aimed to investigate the association between single-nucleotide polymorphisms and spirometric indices in chronic obstructive pulmonary disease and non-chronic obstructive pulmonary disease patients and assess the correlation of these single-nucleotide polymorphisms with pulmonary ventilation function.
View Article and Find Full Text PDFClinics (Sao Paulo)
August 2025
People's Hospital of Zhengzhou University, Zhengzhou, China; Department of Geriatric Medicine, Henan Provincial People's Hospital and Provincial Hospital Clinical Medical College of Zhengzhou University, Zhengzhou, China. Electronic address:
Background: Research has shown that long noncoding RNAs (lncRNAs) play a role in Idiopathic Pulmonary Fibrosis (IPF), but their specific functions and patterns of expression are still unclear.
Method: A diagnostic study was conducted by utilizing analysis techniques. RNA sequencing (RNA-seq) data from 12 IPF patients and 5 controls was used to study lncRNA functions in IPF.
Front Genet
June 2025
Institute of Animal Breeding and Husbandry, Christian-Albrechts-University Kiel, Kiel, Germany.
Background: Beef on Dairy (BoD) calves are born from the crossing of dairy cows with beef breeds. The genetic architecture of these calves differs significantly from the parent breeds due to heterosis and other dominance effects. Identification of the genomic regions associated with traits in BoD calves and the inheritance pattern of these regions can assist in the selection process.
View Article and Find Full Text PDFJ Bras Pneumol
June 2025
. Departamento de Biologia Geral, Universidade Federal Fluminense, Niterói (RJ), Brasil.
Objective: Tuberculosis (TB) is an infectious disease caused by the bacillus Mycobacterium tuberculosis, which was recognized by the World Health Organization (WHO) as a global epidemic in 1993. TB is the leading infectious disease associated with silicosis, with studies showing an increased risk when compared to healthy individuals. We conducted an association study to evaluate the influence of polymorphisms in the ACE, FAM13A, FAS, FASLG, IL1RN, NOS2, TGFB1, and TNF genes on TB susceptibility.
View Article and Find Full Text PDFSci Rep
March 2025
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
Some genetic variants are associated with lung function decline and chronic obstructive pulmonary disease (COPD), but functional studies are necessary to confirm causality. We investigated the genetic susceptibility-associated lung function decline with or without COPD, using data from a community-based cohort (N = 8554). A genome-wide interaction study was conducted to identify the association between genetic variants and pulmonary function, and the way variants relate to lung impairment in accordance with smoking status and amount was examined.
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