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  1. Article: Fatty acids and their lipid mediators in the induction of cellular apoptosis in cancer cells.

    Biswas, Pritam / Datta, Chandreyee / Rathi, Parul / Bhattacharjee, Ashish

    Prostaglandins & other lipid mediators

    2022  Volume 160, Page(s) 106637

    Abstract: The oxygenation of polyunsaturated fatty acids such as arachidonic and linoleic acid through enzymes like lipoxygenases (LOXs) are common and often leads to the production of various bioactive lipids that are important both in acute inflammation and its ... ...

    Abstract The oxygenation of polyunsaturated fatty acids such as arachidonic and linoleic acid through enzymes like lipoxygenases (LOXs) are common and often leads to the production of various bioactive lipids that are important both in acute inflammation and its resolution and thus in disease progression. Amongst the several isoforms of LOX that are expressed in mammals, 15-lipoxygenase (15-LOX) has shown to be crucial in the context of inflammation. Moreover, being expressed in cells of the immune system, as well as in epithelial cells; the enzyme has been shown to crosstalk with a number of important signalling pathways. Mounting evidences from recent reports suggest that 15-LOX has anti-cancer activities which are dependent or independent of its metabolites, and is executed through several downstream pathways like cGMP, PPAR, p53, p21 and NAG-1. However, it is still unclear whether the up-regulation of 15-LOX is associated with cancer cell apoptosis. Monoamine oxidase A (MAO-A), on the other hand, is a mitochondrial flavoenzyme which is believed to be involved in the pathogenesis of atherosclerosis and inflammation and in many other neurological disorders. MAO-A has also been reported as a potential therapeutic target in different types of cancers like prostate cancer, lung cancer etc. In this review, we discussed about the role of fatty acids and their lipid mediators in cancer cell apoptosis. Here we particularly focused on the contribution of oxidative enzymes like 15-LOX and MAO-A in mediating apoptosis in lung cancer cell after fatty acid induction.
    MeSH term(s) Animals ; Apoptosis ; Fatty Acids ; Inflammation ; Lung Neoplasms ; Mammals ; Monoamine Oxidase
    Chemical Substances Fatty Acids ; Monoamine Oxidase (EC 1.4.3.4)
    Language English
    Publishing date 2022-03-24
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 1426962-4
    ISSN 2212-196X ; 1098-8823 ; 0090-6980
    ISSN (online) 2212-196X
    ISSN 1098-8823 ; 0090-6980
    DOI 10.1016/j.prostaglandins.2022.106637
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: NapA (Rv0430), a Novel Nucleoid-Associated Protein that Regulates a Virulence Operon in Mycobacterium tuberculosis in a Supercoiling-Dependent Manner.

    Datta, Chandreyee / Jha, Rajiv Kumar / Ganguly, Sohini / Nagaraja, Valakunja

    Journal of molecular biology

    2019  Volume 431, Issue 8, Page(s) 1576–1591

    Abstract: Comparison of Mycobacterium tuberculosis with Escherichia coli reveals a reduction in the diversity of DNA-managing proteins, such as DNA topoisomerases, although genome sizes are similar for the two species. The same is true for nucleoid-associated ... ...

    Abstract Comparison of Mycobacterium tuberculosis with Escherichia coli reveals a reduction in the diversity of DNA-managing proteins, such as DNA topoisomerases, although genome sizes are similar for the two species. The same is true for nucleoid-associated proteins (NAPs), important factors in bacterial chromosome compaction, chromosome remodeling, and regulation of gene expression. In a search for still uncharacterized NAPs, we found that M. tuberculosis protein Rv0430 has NAP-like features: it binds to DNA in a length- and supercoil-dependent fashion, prefers A/T-rich DNA sequences, protects DNA from damaging agents, and modulates DNA supercoiling. At a ratio of 1 dimer/40 bps of DNA, Rv0430 bridges distant DNA segments; at 1 dimer/20 bps, it coats DNA, forming inflexible rods. Rv0430 also stimulates the DNA relaxation activity of topoisomerase I. Remarkably, Rv0430 stimulates its own promoter in a supercoil-dependent manner. It is the first gene of an operon harboring two regulators of M. tuberculosis virulence (virR and sodC), and controls the expression of these downstream virulence regulators and therefore itself is a virulence regulator. The sensitivity of rv0430 expression to supercoiling is consistent with supercoiling being important for infection by M. tuberculosis. Thus, Rv0430 is a novel NAP, doubling up as a topology modulator of M. tuberculosis.
    MeSH term(s) Amino Acid Sequence ; Animals ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Base Sequence ; DNA, Bacterial/chemistry ; DNA, Bacterial/genetics ; DNA, Bacterial/metabolism ; Gene Expression Regulation, Bacterial ; Humans ; Mycobacterium tuberculosis/chemistry ; Mycobacterium tuberculosis/enzymology ; Mycobacterium tuberculosis/genetics ; Mycobacterium tuberculosis/pathogenicity ; Nitrate Reductase/genetics ; Nitrate Reductase/metabolism ; Operon ; Protein Multimerization ; Tuberculosis/microbiology ; Virulence
    Chemical Substances Bacterial Proteins ; DNA, Bacterial ; Nitrate Reductase (EC 1.7.99.4)
    Language English
    Publishing date 2019-03-12
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2019.02.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: NapA (Rv0430), a Novel Nucleoid-Associated Protein that Regulates a Virulence Operon in Mycobacterium tuberculosis in a Supercoiling-Dependent Manner

    Datta, Chandreyee / Jha, Rajiv Kumar / Ganguly, Sohini / Nagaraja, Valakunja

    Journal of molecular biology. 2019 Apr. 05, v. 431, no. 8

    2019  

    Abstract: Comparison of Mycobacterium tuberculosis with Escherichia coli reveals a reduction in the diversity of DNA-managing proteins, such as DNA topoisomerases, although genome sizes are similar for the two species. The same is true for nucleoid-associated ... ...

    Abstract Comparison of Mycobacterium tuberculosis with Escherichia coli reveals a reduction in the diversity of DNA-managing proteins, such as DNA topoisomerases, although genome sizes are similar for the two species. The same is true for nucleoid-associated proteins (NAPs), important factors in bacterial chromosome compaction, chromosome remodeling, and regulation of gene expression. In a search for still uncharacterized NAPs, we found that M. tuberculosis protein Rv0430 has NAP-like features: it binds to DNA in a length- and supercoil-dependent fashion, prefers A/T-rich DNA sequences, protects DNA from damaging agents, and modulates DNA supercoiling. At a ratio of 1 dimer/40 bps of DNA, Rv0430 bridges distant DNA segments; at 1 dimer/20 bps, it coats DNA, forming inflexible rods. Rv0430 also stimulates the DNA relaxation activity of topoisomerase I. Remarkably, Rv0430 stimulates its own promoter in a supercoil-dependent manner. It is the first gene of an operon harboring two regulators of M. tuberculosis virulence (virR and sodC), and controls the expression of these downstream virulence regulators and therefore itself is a virulence regulator. The sensitivity of rv0430 expression to supercoiling is consistent with supercoiling being important for infection by M. tuberculosis. Thus, Rv0430 is a novel NAP, doubling up as a topology modulator of M. tuberculosis.
    Keywords DNA ; DNA topoisomerase ; DNA-binding proteins ; Escherichia coli ; Mycobacterium tuberculosis ; chromosomes ; enzyme activity ; gene expression regulation ; nucleotide sequences ; operon ; topology ; virulence
    Language English
    Dates of publication 2019-0405
    Size p. 1576-1591.
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2019.02.029
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Physical and functional interaction between nucleoid-associated proteins HU and Lsr2 of Mycobacterium tuberculosis: altered DNA binding and gene regulation.

    Datta, Chandreyee / Jha, Rajiv Kumar / Ahmed, Wareed / Ganguly, Sohini / Ghosh, Soumitra / Nagaraja, Valakunja

    Molecular microbiology

    2019  Volume 111, Issue 4, Page(s) 981–994

    Abstract: Nucleoid-associated proteins (NAPs) in bacteria contribute to key activities such as DNA compaction, chromosome organization and regulation of gene expression. HU and Lsr2 are two principal NAPs in Mycobacterium tuberculosis (Mtb). HU is essential for ... ...

    Abstract Nucleoid-associated proteins (NAPs) in bacteria contribute to key activities such as DNA compaction, chromosome organization and regulation of gene expression. HU and Lsr2 are two principal NAPs in Mycobacterium tuberculosis (Mtb). HU is essential for Mtb survival and is one of the most abundant NAPs. It differs from other eubacterial HU proteins in having a long, flexible lysine- and arginine-rich carboxy-terminal domain. Lsr2 of Mtb is the functional analogue of the bacterial NAP commonly called H-NS. Lsr2 binds to and regulates expression of A/T-rich portions of the otherwise G/C-rich mycobacterial chromosome. Here, we demonstrate that HU and Lsr2 interact to form a complex. The interaction occurs primarily through the flexible carboxy-terminal domain of HU and the acidic amino-terminal domain of Lsr2. The resulting complex, upon binding to DNA, forms thick nucleoprotein rods, in contrast to the DNA bridging seen with Lsr2 and the DNA compaction seen with HU. Furthermore, transcription assays indicate that the HU-Lsr2 complex is a regulator of gene expression. This physical and functional interaction between two NAPs, which has not been reported previously, is likely to be important for DNA organization and gene expression in Mtb and perhaps other bacterial species.
    MeSH term(s) Bacterial Proteins/metabolism ; Chromosomes, Bacterial ; DNA, Bacterial/metabolism ; DNA-Binding Proteins/metabolism ; Gene Expression Regulation, Bacterial ; Mycobacterium tuberculosis/genetics ; Mycobacterium tuberculosis/metabolism
    Chemical Substances Bacterial Proteins ; DNA, Bacterial ; DNA-Binding Proteins ; Lsr2 protein, Mycobacterium tuberculosis ; histone-like protein HU, bacteria
    Language English
    Publishing date 2019-02-11
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 619315-8
    ISSN 1365-2958 ; 0950-382X
    ISSN (online) 1365-2958
    ISSN 0950-382X
    DOI 10.1111/mmi.14202
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Regulation of RNA methylation by therapy treatment, promotes tumor survival.

    Bukhari, Syed Ia / Truesdell, Samuel S / Datta, Chandreyee / Choudhury, Pritha / Wu, Keith Q / Shrestha, Jitendra / Maharjan, Ruby / Plotsker, Ethan / Elased, Ramzi / Laisa, Sadia / Bhambhani, Vijeta / Lin, Yue / Kreuzer, Johannes / Morris, Robert / Koh, Siang-Boon / Ellisen, Leif W / Haas, Wilhelm / Ly, Amy / Vasudevan, Shobha

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Our data previously revealed that chemosurviving cancer cells translate specific genes. Here, we find that the m6A-RNA-methyltransferase, METTL3, increases transiently in chemotherapy-treated breast cancer and leukemic cells in vitro and in vivo. ... ...

    Abstract Our data previously revealed that chemosurviving cancer cells translate specific genes. Here, we find that the m6A-RNA-methyltransferase, METTL3, increases transiently in chemotherapy-treated breast cancer and leukemic cells in vitro and in vivo. Consistently, m6A increases on RNA from chemo-treated cells, and is needed for chemosurvival. This is regulated by eIF2α phosphorylation and mTOR inhibition upon therapy treatment. METTL3 mRNA purification reveals that eIF3 promotes METTL3 translation that is reduced by mutating a 5'UTR m6A-motif or depleting METTL3. METTL3 increase is transient after therapy treatment, as metabolic enzymes that control methylation and thus m6A levels on METTL3 RNA, are altered over time after therapy. Increased METTL3 reduces proliferation and anti-viral immune response genes, and enhances invasion genes, which promote tumor survival. Consistently, overriding phospho-eIF2α prevents METTL3 elevation, and reduces chemosurvival and immune-cell migration. These data reveal that therapy-induced stress signals transiently upregulate METTL3 translation, to alter gene expression for tumor survival.
    Language English
    Publishing date 2023-05-20
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.05.19.540602
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Long-read sequencing reveals complex patterns of wraparound transcription in polyomaviruses.

    Nomburg, Jason / Zou, Wei / Frost, Thomas C / Datta, Chandreyee / Vasudevan, Shobha / Starrett, Gabriel J / Imperiale, Michael J / Meyerson, Matthew / DeCaprio, James A

    PLoS pathogens

    2022  Volume 18, Issue 4, Page(s) e1010401

    Abstract: Polyomaviruses (PyV) are ubiquitous pathogens that can cause devastating human diseases. Due to the small size of their genomes, PyV utilize complex patterns of RNA splicing to maximize their coding capacity. Despite the importance of PyV to human ... ...

    Abstract Polyomaviruses (PyV) are ubiquitous pathogens that can cause devastating human diseases. Due to the small size of their genomes, PyV utilize complex patterns of RNA splicing to maximize their coding capacity. Despite the importance of PyV to human disease, their transcriptome architecture is poorly characterized. Here, we compare short- and long-read RNA sequencing data from eight human and non-human PyV. We provide a detailed transcriptome atlas for BK polyomavirus (BKPyV), an important human pathogen, and the prototype PyV, simian virus 40 (SV40). We identify pervasive wraparound transcription in PyV, wherein transcription runs through the polyA site and circles the genome multiple times. Comparative analyses identify novel, conserved transcripts that increase PyV coding capacity. One of these conserved transcripts encodes superT, a T antigen containing two RB-binding LxCxE motifs. We find that superT-encoding transcripts are abundant in PyV-associated human cancers. Together, we show that comparative transcriptomic approaches can greatly expand known transcript and coding capacity in one of the simplest and most well-studied viral families.
    MeSH term(s) BK Virus/genetics ; Humans ; Polyomavirus/genetics ; Polyomavirus Infections/genetics ; RNA Splicing ; Simian virus 40/genetics
    Language English
    Publishing date 2022-04-01
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2205412-1
    ISSN 1553-7374 ; 1553-7374
    ISSN (online) 1553-7374
    ISSN 1553-7374
    DOI 10.1371/journal.ppat.1010401
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Localized outbreaks of

    Pulusu, Chanakya Pachi / Manivannan, Bhavani / Raman, Sai Suguna / Singh, Sanjay / Khamari, Balaram / Lama, Manmath / Peketi, Arun Sai Kumar / Datta, Chandreyee / Prasad, Kashi Nath / Nagaraja, Valakunja / Pradeep, Bulagonda Eswarappa

    Journal of medical microbiology

    2022  Volume 71, Issue 3

    Abstract: ... ...

    Abstract Introduction
    MeSH term(s) Clone Cells ; Disease Outbreaks ; Hospitals ; Humans ; Pseudomonas Infections/microbiology ; Pseudomonas aeruginosa
    Language English
    Publishing date 2022-03-14
    Publishing country England
    Document type Journal Article
    ZDB-ID 218356-0
    ISSN 1473-5644 ; 0022-2615
    ISSN (online) 1473-5644
    ISSN 0022-2615
    DOI 10.1099/jmm.0.001500
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Ribosome changes reprogram translation for chemosurvival in G0 leukemic cells.

    Datta, Chandreyee / Truesdell, Samuel S / Wu, Keith Q / Bukhari, Syed I A / Ngue, Harrison / Buchanan, Brienna / Le Tonqueze, Olivier / Lee, Sooncheol / Kollu, Swapna / Granovetter, Madeleine A / Boukhali, Myriam / Kreuzer, Johannes / Batool, Maheen S / Balaj, Leonora / Haas, Wilhelm / Vasudevan, Shobha

    Science advances

    2022  Volume 8, Issue 43, Page(s) eabo1304

    Abstract: Quiescent leukemic cells survive chemotherapy, with translation changes. Our data reveal that FXR1, a protein amplified in several aggressive cancers, is elevated in quiescent and chemo-treated leukemic cells and promotes chemosurvival. This suggests ... ...

    Abstract Quiescent leukemic cells survive chemotherapy, with translation changes. Our data reveal that FXR1, a protein amplified in several aggressive cancers, is elevated in quiescent and chemo-treated leukemic cells and promotes chemosurvival. This suggests undiscovered roles for this RNA- and ribosome-associated protein in chemosurvival. We find that FXR1 depletion reduces translation, with altered rRNAs, snoRNAs, and ribosomal proteins (RPs). FXR1 regulates factors that promote transcription and processing of ribosomal genes and snoRNAs. Ribosome changes in FXR1-overexpressing cells, including RPLP0/uL10 levels, activate eIF2α kinases. Accordingly, phospho-eIF2α increases, enabling selective translation of survival and immune regulators in FXR1-overexpressing cells. Overriding these genes or phospho-eIF2α with inhibitors reduces chemosurvival. Thus, elevated FXR1 in quiescent or chemo-treated leukemic cells alters ribosomes that trigger stress signals to redirect translation for chemosurvival.
    Language English
    Publishing date 2022-10-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2810933-8
    ISSN 2375-2548 ; 2375-2548
    ISSN (online) 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.abo1304
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: The secreted antigen, HP0175, of Helicobacter pylori links the unfolded protein response (UPR) to autophagy in gastric epithelial cells.

    Halder, Priyanka / Datta, Chandreyee / Kumar, Ranjeet / Sharma, Arun Kumar / Basu, Joyoti / Kundu, Manikuntala

    Cellular microbiology

    2015  Volume 17, Issue 5, Page(s) 714–729

    Abstract: Autophagy is an intracellular catabolic process that is required to maintain cellular homeostasis. Pathogen-elicited host cell autophagy may favour containment of infection or may help in bacterial survival. Pathogens have developed the ability to ... ...

    Abstract Autophagy is an intracellular catabolic process that is required to maintain cellular homeostasis. Pathogen-elicited host cell autophagy may favour containment of infection or may help in bacterial survival. Pathogens have developed the ability to modulate host autophagy. The secreted antigen HP0175, a peptidyl prolyl cis,trans isomerase of Helicobacter pylori, has moonlighting functions with reference to host cells. Here we show that it executes autophagy in gastric epithelial cells. Autophagy is dependent on the unfolded protein response (UPR) that activates the expression of PKR-like ER kinase (PERK). This is accompanied by phosphorylation of eukaryotic initiation factor 2α (eIF-2α) and transcriptional activation of ATF4 and CHOP. Knockdown of UPR-related genes inhibits the conversion of LC3I to LC3II, a marker of autophagy. The autophagy-inducing ability of H. pylori is compromised when cells are infected with an isogenic hp0175 mutant. Autophagy precedes apoptosis. Silencing of BECLIN1 augments cleavage of caspase 3 as well as apoptosis. Increased apoptosis of gastric epithelial cells is known to be linked to H. pylori-mediated gastric inflammation and carcinogenesis. To the best of our knowledge, this study provides the first demonstration of how HP0175 endowed with moonlighting functions links UPR-dependent autophagy and apoptosis during H. pylori infection.
    MeSH term(s) Antigens, Bacterial/metabolism ; Autophagy/drug effects ; Epithelial Cells/drug effects ; Epithelial Cells/microbiology ; Epithelial Cells/physiology ; Helicobacter pylori/physiology ; Host-Pathogen Interactions ; Peptidylprolyl Isomerase/metabolism ; Signal Transduction ; Unfolded Protein Response/drug effects
    Chemical Substances Antigens, Bacterial ; Peptidylprolyl Isomerase (EC 5.2.1.8)
    Language English
    Publishing date 2015-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1468320-9
    ISSN 1462-5822 ; 1462-5814
    ISSN (online) 1462-5822
    ISSN 1462-5814
    DOI 10.1111/cmi.12396
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Genome-wide mRNA-miRNA profiling uncovers a role of the microRNA miR-29b-1-5p/PHLPP1 signalling pathway in Helicobacter pylori-driven matrix metalloproteinase production in gastric epithelial cells.

    Datta, Chandreyee / Subuddhi, Arijita / Kumar, Manish / Lepcha, Thurbu Tshering / Chakraborty, Sohini / Jana, Kuladip / Ghosh, Zhumur / Mukhopadhyay, Asish Kumar / Basu, Joyoti / Kundu, Manikuntala

    Cellular microbiology

    2018  Volume 20, Issue 9, Page(s) e12859

    Abstract: Aberrant expression of microRNAs (miRNAs) is associated with tumour progression, extracellular matrix remodelling, and cell proliferation. miRNAs modulate host gene expression during infection by pathogens such as Helicobacter pylori, which is associated ...

    Abstract Aberrant expression of microRNAs (miRNAs) is associated with tumour progression, extracellular matrix remodelling, and cell proliferation. miRNAs modulate host gene expression during infection by pathogens such as Helicobacter pylori, which is associated with varying degrees of gastric pathology. In order to gain insight into the regulation of gene expression by miRNAs during H. pylori infection of gastric epithelial cells and its likely downstream consequences, we analysed the transcriptomes and miRnomes of AGS cells infected with H. pylori. In silico analysis of miRNA-mRNA interactions suggested that miR-29b-1-5p was a likely regulator of pathways associated with gastric epithelial cell pathology. We validated PH domain leucine rich phosphatase 1 (PHLPP1), a negative regulator of the Akt signalling pathway, as a target of miR-29b-1-5p. In an in vivo mouse model, we observed that infection with H. pylori was associated with upregulation of miR-29b-1-5p and downregulation of PHLPP1. Transfection with either a mimic or an inhibitor of miR-29b-1-5p confirmed that downregulation of PHLPP1 upregulates Akt-dependent NF-κB signalling leading to activation of matrix metalloproteinases 2 and 9, players in the degradation of extracellular matrix during H. pylori infection. The secreted antigen HP0175 was associated with upregulation of miR-29b-1-5p, regulation of metalloproteinase activity, and migration of AGS cells. Our study suggests that targeting the miR-29b-1-5p/PHLPP1 signalling axis could be a potential host-directed approach for regulating the outcome of H. pylori infection.
    MeSH term(s) Animals ; Cell Line ; Disease Models, Animal ; Epithelial Cells/microbiology ; Gene Expression Profiling ; Gene Regulatory Networks ; Helicobacter Infections/pathology ; Helicobacter pylori/growth & development ; Host-Pathogen Interactions ; Matrix Metalloproteinase 2/metabolism ; Matrix Metalloproteinase 9/metabolism ; Mice ; MicroRNAs/metabolism ; Nuclear Proteins/metabolism ; Phosphoprotein Phosphatases/metabolism ; Signal Transduction
    Chemical Substances MIRN29 microRNA, mouse ; MicroRNAs ; Nuclear Proteins ; Phlpp protein, mouse (EC 3.1.3.16) ; Phosphoprotein Phosphatases (EC 3.1.3.16) ; Matrix Metalloproteinase 2 (EC 3.4.24.24) ; Mmp2 protein, mouse (EC 3.4.24.24) ; Matrix Metalloproteinase 9 (EC 3.4.24.35) ; Mmp9 protein, mouse (EC 3.4.24.35)
    Language English
    Publishing date 2018-05-25
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1468320-9
    ISSN 1462-5822 ; 1462-5814
    ISSN (online) 1462-5822
    ISSN 1462-5814
    DOI 10.1111/cmi.12859
    Database MEDical Literature Analysis and Retrieval System OnLINE

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