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1.
Microbes Infect ; 26(1-2): 105246, 2024.
Article in English | MEDLINE | ID: mdl-37926369

ABSTRACT

The delivery of Helicobacter pylori CagA into host cells was long believed to occur through the integrin cell surface receptors. However, the role of CEACAM receptors has recently been highlighted, instead. Here, we have categorized the existing experimental evidence according to whether deletion, upregulation, downregulation, or inhibition of the target ligands (T4SS or HopQ) or receptors (integrins or CEACAMs), result in alterations in CagA phosphorylation, cell elongation, or IL-8 production. According to our analysis, the statistics favor the essence of most of the T4SS constituents and the involvement of HopQ adhesin in all three functions. Concerning the integrin family, the collected data is controversial, but yielding towards it being dispensable or involved in CagA translocation. Yet, regarding cell elongation, more events are showing ß1 integrin being involved, than αvß4 being inhibitory. Concerning IL-8 secretion, again there are more events showing α5, ß1 and ß6 integrins to be involved, than those showing inhibitory roles for ß1, ß4 and ß6 integrins. Finally, CEACAM 1, 3, and 5 are identified as mostly essential or involved in CagA phosphorylation, whereasCEACAM 4, 7, and 8 are found dispensable and CEACAM6 is under debate. Conversely, CEACAM1, 5 and 6 appear mostly dispensable for cell elongation. Noteworthy is the choice of cell type, bacterial strain, multiplicity and duration of infection, as well as the sensitivity of the detection methods, all of which can affect the variably obtained results.


Subject(s)
Helicobacter Infections , Helicobacter pylori , Humans , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Integrins/metabolism , Antigens, Bacterial/genetics , Antigens, Bacterial/metabolism , Helicobacter pylori/genetics , Interleukin-8/metabolism
2.
Genome Biol ; 24(1): 178, 2023 08 03.
Article in English | MEDLINE | ID: mdl-37537644

ABSTRACT

Differential gene expression in bulk transcriptomics data can reflect change of transcript abundance within a cell type and/or change in the proportions of cell types. Expression deconvolution methods can help differentiate these scenarios. BEDwARS is a Bayesian deconvolution method designed to address differences between reference signatures of cell types and corresponding true signatures underlying bulk transcriptomic profiles. BEDwARS is more robust to noisy reference signatures and outperforms leading in-class methods for estimating cell type proportions and signatures. Application of BEDwARS to dihydropyridine dehydrogenase deficiency identified the possible involvement of ciliopathy and impaired translational control in the etiology of the disorder.


Subject(s)
Gene Expression Profiling , Transcriptome , Bayes Theorem , Gene Expression Profiling/methods
3.
Genome Biol ; 22(1): 19, 2021 01 07.
Article in English | MEDLINE | ID: mdl-33413550

ABSTRACT

BACKGROUND: Metastatic progress is the primary cause of death in most cancers, yet the regulatory dynamics driving the cellular changes necessary for metastasis remain poorly understood. Multi-omics approaches hold great promise for addressing this challenge; however, current analysis tools have limited capabilities to systematically integrate transcriptomic, epigenomic, and cistromic information to accurately define the regulatory networks critical for metastasis. RESULTS: To address this limitation, we use a purposefully generated cellular model of colon cancer invasiveness to generate multi-omics data, including expression, accessibility, and selected histone modification profiles, for increasing levels of invasiveness. We then adopt a rigorous probabilistic framework for joint inference from the resulting heterogeneous data, along with transcription factor binding profiles. Our approach uses probabilistic graphical models to leverage the functional information provided by specific epigenomic changes, models the influence of multiple transcription factors simultaneously, and automatically learns the activating or repressive roles of cis-regulatory events. Global analysis of these relationships reveals key transcription factors driving invasiveness, as well as their likely target genes. Disrupting the expression of one of the highly ranked transcription factors JunD, an AP-1 complex protein, confirms functional relevance to colon cancer cell migration and invasion. Transcriptomic profiling confirms key regulatory targets of JunD, and a gene signature derived from the model demonstrates strong prognostic potential in TCGA colorectal cancer data. CONCLUSIONS: Our work sheds new light into the complex molecular processes driving colon cancer metastasis and presents a statistically sound integrative approach to analyze multi-omics profiles of a dynamic biological process.


Subject(s)
Neoplasm Metastasis/genetics , Neoplasms/genetics , Neoplasms/metabolism , Cell Line, Tumor , Cell Movement , Colonic Neoplasms/genetics , Colonic Neoplasms/metabolism , Epigenomics , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Histones , Humans , Prognosis , Proto-Oncogene Proteins c-jun/genetics , Transcription Factor AP-1 , Transcription Factors/metabolism , Transcriptome
4.
Sci Rep ; 8(1): 5873, 2018 04 12.
Article in English | MEDLINE | ID: mdl-29651001

ABSTRACT

Consumption of green tea (GT) extracts or purified catechins has shown the ability to prevent oral and other cancers and inhibit cancer progression in rodent models, but the evidence for this in humans is mixed. Working with humans, we sought to understand the source of variable responses to GT by examining its effects on oral epithelium. Lingual epithelial RNA and lingual and gingival microbiota were measured before and after 4 weeks of exposure in tobacco smokers, whom are at high risk of oral cancer. GT consumption had on average inconsistent effects on miRNA expression in the oral epithelium. Only analysis that examined paired miRNAs, showing changed and coordinated expression with GT exposure, provided evidence for a GT effect on miRNAs, identifying miRNAs co-expressed with two hubs, miR-181a-5p and 301a-3p. An examination of the microbiome on cancer prone lingual mucosa, in contrast, showed clear shifts in the relative abundance of Streptococcus and Staphylococcus, and other genera after GT exposure. These data support the idea that tea consumption can consistently change oral bacteria in humans, which may affect carcinogenesis, but argue that GT effects on oral epithelial miRNA expression in humans vary between individuals.


Subject(s)
Antioxidants/administration & dosage , MicroRNAs/genetics , Mouth Mucosa/drug effects , Mouth Neoplasms/prevention & control , Tea/chemistry , Adult , Antioxidants/chemistry , Carcinogenesis/drug effects , Catechin/administration & dosage , Epithelium/drug effects , Epithelium/microbiology , Female , Gene Expression Regulation, Neoplastic/drug effects , Gingiva/drug effects , Gingiva/microbiology , Humans , Male , MicroRNAs/drug effects , Microbiota/drug effects , Microbiota/genetics , Middle Aged , Mouth Mucosa/microbiology , Mouth Neoplasms/genetics , Mouth Neoplasms/microbiology , Smokers , Staphylococcus/drug effects , Staphylococcus/pathogenicity , Streptococcus/drug effects , Streptococcus/pathogenicity , Young Adult
5.
Iran J Psychiatry ; 12(2): 142-146, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28659987

ABSTRACT

Objective: Management of borderline personality disorder (BPD) is a difficult challenge due to the complex features of this disorder. This article reviews the use of naltrexone in the treatment of BPD. Method: Published articles and clinical trials were searched in Google Scholar, MedLine, ELSEVIER, and Cochrane database of systematic reviews abstracts in English language between 1990 and 2017. Results: Naltrexone (NTX), a nonspecific competitive opiate antagonist, has been noted to be helpful in controlling self-injurious behavior (SIB) and dissociative symptoms in patients with BPD. Conclusion: Further studies should be conducted on the effects of naltrexone to confirm the role of this medication in the treatment of BPD.

6.
J Res Pharm Pract ; 3(4): 142-4, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25535623

ABSTRACT

Superwarfarin toxicity may be a serious problem. It needs high clinical suspicious in patients with bleeding diathesis without hematologic or liver diseases even in patients with apparent negative history of warfarin or other anticoagulant accessibility. Here we reported a patient with a negative history of any medical diseases or drug administration who was referred with generalized ecchymosis. Increased international normalized ratio and decreased vitamin K-dependent coagulation factors were detected in this patient. His hematologic and liver evaluations were normal. Clinical pharmacist emphasis in taking history revealed using anticoagulant rodenticide all over the farm the patient lived in that might result in unaware intoxication in this patient who suffered dementia.

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