Publications by authors named "Amir Foroushani"

Article Synopsis
  • Interferon-stimulated genes (ISGs) are crucial for the body's immune defenses, but when overactive, they can contribute to inflammatory diseases and interfere with normal immune function.* -
  • Research on MATRIN3 (MATR3), a protein linked to familial ALS, shows that disrupting MATR3 increases ISG expression, revealing a potential pathway related to ALS development.* -
  • The findings suggest that this pathway, involving cGAS-STING activation, could lead to new diagnostic and treatment strategies for certain cases of ALS.*
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Suppressive regulatory T cell (Treg) differentiation is controlled by diverse immunometabolic signaling pathways and intracellular metabolites. Here we show that cell-permeable α-ketoglutarate (αKG) alters the DNA methylation profile of naive CD4 T cells activated under Treg polarizing conditions, markedly attenuating FoxP3+ Treg differentiation and increasing inflammatory cytokines. Adoptive transfer of these T cells into tumor-bearing mice results in enhanced tumor infiltration, decreased FoxP3 expression, and delayed tumor growth.

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  • The human genome encodes over 1,500 RNA-binding proteins (RBPs), but most research has focused on their effects on protein-coding mRNAs, leaving a neglected area involving endogenous retroviruses (ERVs), which make up about 8% of the genome.
  • This study aimed to explore the interaction between RBPs and ERV transcripts, using a computational approach to correlate their expressions in RNA-sequencing data.
  • The findings highlight RNA-binding motif protein 4 (RBM4) as a key regulator that binds to ERV transcripts and represses their expression, specifically noting its effect on HERV-K elements through a conserved CGG element.
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  • Fetal hematopoietic stem and progenitor cells (HSPCs) show potential for treating blood-related diseases, and previous research indicated that the RNA-binding protein Lin28b helps adult HSPCs mimic fetal cells.
  • New findings reveal that Lin28b alone cannot fully change adult HSPC gene expression to fetal patterns, but its partnership with another RNA-binding protein, Igf2bp3, significantly boosts this process.
  • The collaboration between Lin28b and Igf2bp3 stabilizes key mRNAs involved in B-cell development, highlighting their role in a regulatory network that influences the transition from fetal to adult hematopoiesis, which may have therapeutic implications.
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Hepatocellular carcinoma (HCC) remains a deadly cancer, underscoring the need for relevant preclinical models. Male C3HeB/FeJ mice model spontaneous HCC with some hepatocarcinogenesis susceptibility loci corresponding to syntenic regions of human chromosomes altered in HCC. We tested other properties of C3HeB/FeJ tumors for similarity to human HCC.

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Network analysis is the preferred approach for the detection of subtle but coordinated changes in expression of an interacting and related set of genes. We introduce a novel method based on the analyses of coexpression networks and Bayesian networks, and we use this new method to classify two types of hematological malignancies; namely, acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Our classifier has an accuracy of 93%, a precision of 98%, and a recall of 90% on the training dataset (n = 366); which outperforms the results reported by other scholars on the same dataset.

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Background: The distinct types of hematological malignancies have different biological mechanisms and prognoses. For instance, myelodysplastic syndrome (MDS) is generally indolent and low risk; however, it may transform into acute myeloid leukemia (AML), which is much more aggressive.

Methods: We develop a novel network analysis approach that uses expression of eigengenes to delineate the biological differences between these two diseases.

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Motivation. Predominant pathway analysis approaches treat pathways as collections of individual genes and consider all pathway members as equally informative. As a result, at times spurious and misleading pathways are inappropriately identified as statistically significant, solely due to components that they share with the more relevant pathways.

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MicroRNAs (miRNAs) are important regulators of gene expression and are known to play a key role in regulating both adaptive and innate immunity. Bovine alveolar macrophages (BAMs) help maintain lung homeostasis and constitute the front line of host defense against several infectious respiratory diseases, such as bovine tuberculosis. Little is known, however, about the role miRNAs play in these cells.

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MicroRNAs (miRNAs) are short, non-coding RNAs, which post-transcriptionally regulate gene expression and are proposed to play a key role in the regulation of innate and adaptive immunity. Here, we report a next generation sequencing (NGS) approach profiling the expression of miRNAs in primary bovine mammary epithelial cells (BMEs) at 1, 2, 4 and 6 hours post-infection with Streptococcus uberis, a causative agent of bovine mastitis. Analysing over 450 million sequencing reads, we found that 20% of the approximately 1,300 currently known bovine miRNAs are expressed in unchallenged BMEs.

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InnateDB (http://www.innatedb.com) is an integrated analysis platform that has been specifically designed to facilitate systems-level analyses of mammalian innate immunity networks, pathways and genes.

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Background: The innate immune response is the first line of defence against invading pathogens and is regulated by complex signalling and transcriptional networks. Systems biology approaches promise to shed new light on the regulation of innate immunity through the analysis and modelling of these networks. A key initial step in this process is the contextual cataloguing of the components of this system and the molecular interactions that comprise these networks.

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