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  1. Article ; Online: LncRTPred: Predicting RNA-RNA mode of interaction mediated by lncRNA.

    Das, Gourab / Das, Troyee / Parida, Sibun / Ghosh, Zhumur

    IUBMB life

    2023  Volume 76, Issue 1, Page(s) 53–68

    Abstract: Long non-coding RNAs (lncRNAs) play a significant role in various biological processes. Hence, it is utmost important to elucidate their functions in order to understand the molecular mechanism of a complex biological system. This versatile RNA molecule ... ...

    Abstract Long non-coding RNAs (lncRNAs) play a significant role in various biological processes. Hence, it is utmost important to elucidate their functions in order to understand the molecular mechanism of a complex biological system. This versatile RNA molecule has diverse modes of interaction, one of which constitutes lncRNA-mRNA interaction. Hence, identifying its target mRNA is essential to understand the function of an lncRNA explicitly. Existing lncRNA target prediction tools mainly adopt thermodynamics approach. Large execution time and inability to perform real-time prediction limit their usage. Further, lack of negative training dataset has been a hindrance in the path of developing machine learning (ML) based lncRNA target prediction tools. In this work, we have developed a ML-based lncRNA-mRNA target prediction model- 'LncRTPred'. Here we have addressed the existing problems by generating reliable negative dataset and creating robust ML models. We have identified the non-interacting lncRNA and mRNAs from the unlabelled dataset using BLAT. It is further filtered to get a reliable set of outliers. LncRTPred provides a cumulative_model_score as the final output against each query. In terms of prediction accuracy, LncRTPred outperforms other popular target prediction protocols like LncTar. Further, we have tested its performance against experimentally validated disease-specific lncRNA-mRNA interactions. Overall, performance of LncRTPred is heavily dependent on the size of the training dataset, which is highly reflected by the difference in its performance for human and mouse species. Its performance for human species shows better as compared to that for mouse when applied on an unknown data due to smaller size of the training dataset in case of mouse compared to that of human. Availability of increased number of lncRNA-mRNA interaction data for mouse will improve the performance of LncRTPred in future. Both webserver and standalone versions of LncRTPred are available. Web server link: http://bicresources.jcbose.ac.in/zhumur/lncrtpred/index.html. Github Link: https://github.com/zglabDIB/LncRTPred.
    MeSH term(s) Humans ; Animals ; Mice ; RNA, Long Noncoding/genetics ; RNA, Messenger/genetics ; Computational Biology/methods
    Chemical Substances RNA, Long Noncoding ; RNA, Messenger
    Language English
    Publishing date 2023-08-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 1492141-8
    ISSN 1521-6551 ; 1521-6543
    ISSN (online) 1521-6551
    ISSN 1521-6543
    DOI 10.1002/iub.2778
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: MicroRNA mediated gene regulatory circuits leads to machine learning based preliminary detection of acute myeloid leukemia.

    Sarkar, Arijita / Das, Troyee / Das, Gourab / Ghosh, Zhumur

    Computational biology and chemistry

    2023  Volume 104, Page(s) 107859

    Abstract: Acute Myeloid Leukemia (AML) can be detected based on morphology, cytochemistry, immunological markers, and cytogenetics. MicroRNAs (miRNAs) influence key biological pathways in multiple haematological malignancies including AML. In this work, we have ... ...

    Abstract Acute Myeloid Leukemia (AML) can be detected based on morphology, cytochemistry, immunological markers, and cytogenetics. MicroRNAs (miRNAs) influence key biological pathways in multiple haematological malignancies including AML. In this work, we have analysed the miRNome and the transcriptome of normal and AML samples and have identified the significant set of miRNA-target mRNA pairs present within AML- Peripheral Blood and AML- Bone Marrow samples from both tissue and cell lines. The miRNA target genes are further filtered based on their functional significance in AML system. These filtered genes constitute the set of selected miRNA target features, which have been finally used for developing machine learning based prediction tool, 'TbAMLPred' for preliminary detection of AML. This model implements both unsupervised clustering and supervised classification algorithms that would increase the reliability of prediction. Our results show that the selected miRNA target-based features can separate the control and disease samples linearly. Overall, we put forward 'TbAMLPred' for a non-invasive mode of preliminary AML diagnosis in future. Github link for accessing TbAMLPred: https://github.com/zglabDIB/TbAMLPred.
    MeSH term(s) Humans ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Reproducibility of Results ; Leukemia, Myeloid, Acute/diagnosis ; Leukemia, Myeloid, Acute/genetics ; Cell Line ; Gene Regulatory Networks/genetics
    Chemical Substances MicroRNAs
    Language English
    Publishing date 2023-03-31
    Publishing country England
    Document type Journal Article
    ISSN 1476-928X
    ISSN (online) 1476-928X
    DOI 10.1016/j.compbiolchem.2023.107859
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Defense Surveillance System at the Interface: Response of Rice Towards

    Acharya, Udita / Das, Troyee / Ghosh, Zhumur / Ghosh, Anupama

    Molecular plant-microbe interactions : MPMI

    2022  , Page(s) MPMI07220153R

    Abstract: Sheath blight of rice caused by necrotrophic plant ... ...

    Abstract Sheath blight of rice caused by necrotrophic plant pathogen
    Language English
    Publishing date 2022-12-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 743331-1
    ISSN 1943-7706 ; 0894-0282
    ISSN (online) 1943-7706
    ISSN 0894-0282
    DOI 10.1094/MPMI-07-22-0153-R
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: NSAID targets SIRT3 to trigger mitochondrial dysfunction and gastric cancer cell death.

    Debsharma, Subhashis / Pramanik, Saikat / Bindu, Samik / Mazumder, Somnath / Das, Troyee / Pal, Uttam / Saha, Debanjan / De, Rudranil / Nag, Shiladitya / Banerjee, Chinmoy / Chandra Maiti, Nakul / Ghosh, Zhumur / Bandyopadhyay, Uday

    iScience

    2024  Volume 27, Issue 4, Page(s) 109384

    Abstract: Gastric cancer (GC) is a deadly malignancy that demands effective therapeutic intervention capitalizing unique drug target/s. Here, we report that indomethacin, a cyclooxygenase non-selective non-steroidal anti-inflammatory drug, arrests GC cell growth ... ...

    Abstract Gastric cancer (GC) is a deadly malignancy that demands effective therapeutic intervention capitalizing unique drug target/s. Here, we report that indomethacin, a cyclooxygenase non-selective non-steroidal anti-inflammatory drug, arrests GC cell growth by targeting mitochondrial deacetylase Sirtuin 3 (SIRT3). Interaction study revealed that indomethacin competitively inhibited SIRT3 by binding to nicotinamide adenine dinucleotide (NAD)-binding site. The Cancer Genome Atlas data meta-analysis indicated poor prognosis associated with high SIRT3 expression in GC. Further, transcriptome sequencing data of human gastric adenocarcinoma cells revealed that indomethacin treatment severely downregulated SIRT3. Indomethacin-induced SIRT3 downregulation augmented SOD2 and OGG1 acetylation, leading to mitochondrial redox dyshomeostasis, mtDNA damage, respiratory chain failure, bioenergetic crisis, mitochondrial fragmentation, and apoptosis via blocking the AMPK/PGC1α/SIRT3 axis. Indomethacin also downregulated SIRT3 regulators ERRα and PGC1α. Further, SIRT3 knockdown aggravated indomethacin-induced mitochondrial dysfunction as well as blocked cell-cycle progression to increase cell death. Thus, we reveal how indomethacin induces GC cell death by disrupting SIRT3 signaling.
    Language English
    Publishing date 2024-03-01
    Publishing country United States
    Document type Journal Article
    ISSN 2589-0042
    ISSN (online) 2589-0042
    DOI 10.1016/j.isci.2024.109384
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: LncRBase V.2: an updated resource for multispecies lncRNAs and ClinicLSNP hosting genetic variants in lncRNAs for cancer patients

    Das, Troyee / Deb, Aritra / Parida, Sibun / Mondal, Sudip / Khatua, Sunirmal / Ghosh, Zhumur

    RNA biology. 2021 Aug. 03, v. 18, no. 8

    2021  

    Abstract: The recent discovery of long non-coding RNA as a regulatory molecule in the cellular system has altered the concept of the functional aptitude of the genome. Since our publication of the first version of LncRBase in 2014, there has been an enormous ... ...

    Abstract The recent discovery of long non-coding RNA as a regulatory molecule in the cellular system has altered the concept of the functional aptitude of the genome. Since our publication of the first version of LncRBase in 2014, there has been an enormous increase in the number of annotated lncRNAs of multiple species other than Human and Mouse. LncRBase V.2 hosts information of 549,648 lncRNAs corresponding to six additional species besides Human and Mouse, viz. Rat, Fruitfly, Zebrafish, Chicken, Cow and C.elegans. It provides additional distinct features such as (i) Transcription Factor Binding Site (TFBS) in the lncRNA promoter region, (ii) sub-cellular localization pattern of lncRNAs (iii) lnc-pri-miRNAs (iv) Possible small open reading frames (sORFs) within lncRNA. (v) Manually curated information of interacting target molecules and disease association of lncRNA genes (vi) Distribution of lncRNAs across multiple tissues of all species. Moreover, we have hosted ClinicLSNP within LncRBase V.2. ClinicLSNP has a comprehensive catalogue of lncRNA variants present within breast, ovarian, and cervical cancer inferred from 561 RNA-Seq data corresponding to these cancers. Further, we have checked whether these lncRNA variants overlap with (i)Repeat elements,(ii)CGI, (iii)TFBS within lncRNA loci (iv)SNP localization in trait-associated Linkage Disequilibrium(LD) region, (v)predicted the potentially pathogenic variants and (vi)effect of SNP on lncRNA secondary structure. Overall, LncRBaseV.2 is a user-friendly database to survey, search and retrieve information about multi-species lncRNAs. Further, ClinicLSNP will serve as a useful resource for cancer specific lncRNA variants and their related information. The database is freely accessible and available at http://dibresources.jcbose.ac.in/zhumur/lncrbase2/.
    Keywords Danio rerio ; breasts ; chickens ; cows ; databases ; fruit flies ; humans ; linkage disequilibrium ; mice ; non-coding RNA ; promoter regions ; rats ; sequence analysis ; surveys ; transcription factors ; uterine cervical neoplasms
    Language English
    Dates of publication 2021-0803
    Size p. 1136-1151.
    Publishing place Taylor & Francis
    Document type Article
    ISSN 1555-8584
    DOI 10.1080/15476286.2020.1833529
    Database NAL-Catalogue (AGRICOLA)

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  6. Article: The Natural Antisense Transcript DONE40 Derived from the lncRNA ENOD40 Locus Interacts with SET Domain Protein ASHR3 During Inception of Symbiosis in Arachis hypogaea

    Ganguly, Pritha / Roy, Dipan / Das, Troyee / Kundu, Anindya / Cartieaux, Fabienne / Ghosh, Zhumur / DasGupta, Maitrayee

    Molecular plant-microbe interactions. 2021 Sept., v. 34, no. 9

    2021  

    Abstract: The long noncoding RNA ENOD40 is required for cortical cell division during root nodule symbiosis (RNS) of legumes, though it is not essential for actinorhizal RNS. Our objective was to understand whether ENOD40 was required for aeschynomenoid nodule ... ...

    Abstract The long noncoding RNA ENOD40 is required for cortical cell division during root nodule symbiosis (RNS) of legumes, though it is not essential for actinorhizal RNS. Our objective was to understand whether ENOD40 was required for aeschynomenoid nodule formation in Arachis hypogaea. AhENOD40 express from chromosome 5 (chr5) (AhENOD40-1) and chr15 (AhENOD40-2) during symbiosis, and RNA interference of these transcripts drastically affected nodulation, indicating the importance of ENOD40 in A. hypogaea. Furthermore, we demonstrated several distinct characteristics of ENOD40. (i) Natural antisense transcript (NAT) of ENOD40 was detected from the AhENOD40-1 locus (designated as NAT-AhDONE40). (ii) Both AhENOD40-1 and AhENOD40-2 had two exons, whereas NAT-AhDONE40 was monoexonic. Reverse-transcription quantitative PCR analysis indicated both sense and antisense transcripts to be present in both cytoplasm and nucleus, and their expression increased with the progress of symbiosis. (iii) RNA pull-down from whole cell extracts of infected roots at 4 days postinfection indicated NAT-AhDONE40 to interact with the SET (Su(var)3-9, enhancer of Zeste and Trithorax) domain containing absent small homeotic disc (ASH) family protein AhASHR3 and this interaction was further validated using RNA immunoprecipitation and electrophoretic mobility shift assay. (iv) Chromatin immunoprecipitation assays indicate deposition of ASHR3-specific histone marks H3K36me3 and H3K4me3 in both of the ENOD40 loci during the progress of symbiosis. ASHR3 is known for its role in optimizing cell proliferation and reprogramming. Because both ASHR3 and ENOD40 from legumes cluster away from those in actinorhizal plants and other nonlegumes in phylogenetic distance trees, we hypothesize that the interaction of DONE40 with ASHR3 could have evolved for adapting the nodule organogenesis program for legumes. Copyright © 2021 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
    Keywords Arachis hypogaea ; RNA interference ; cell division ; cell proliferation ; chromatin immunoprecipitation ; cytoplasm ; exons ; gel electrophoresis ; genetic distance ; histones ; loci ; nodulation ; non-coding RNA ; organogenesis ; quantitative polymerase chain reaction ; reverse transcription ; root nodules ; symbiosis
    Language English
    Dates of publication 2021-09
    Size p. 1057-1070.
    Publishing place The American Phytopathological Society
    Document type Article
    ZDB-ID 743331-1
    ISSN 1943-7706 ; 0894-0282
    ISSN (online) 1943-7706
    ISSN 0894-0282
    DOI 10.1094/MPMI-12-20-0357-R
    Database NAL-Catalogue (AGRICOLA)

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  7. Article ; Online: LncRBase V.2: an updated resource for multispecies lncRNAs and ClinicLSNP hosting genetic variants in lncRNAs for cancer patients.

    Das, Troyee / Deb, Aritra / Parida, Sibun / Mondal, Sudip / Khatua, Sunirmal / Ghosh, Zhumur

    RNA biology

    2020  Volume 18, Issue 8, Page(s) 1136–1151

    Abstract: The recent discovery of long non-coding RNA as a regulatory molecule in the cellular system has altered the concept of the functional aptitude of the genome. Since our publication of the first version of LncRBase in 2014, there has been an enormous ... ...

    Abstract The recent discovery of long non-coding RNA as a regulatory molecule in the cellular system has altered the concept of the functional aptitude of the genome. Since our publication of the first version of LncRBase in 2014, there has been an enormous increase in the number of annotated lncRNAs of multiple species other than Human and Mouse. LncRBase V.2 hosts information of 549,648 lncRNAs corresponding to six additional species besides Human and Mouse, viz. Rat, Fruitfly, Zebrafish, Chicken, Cow and
    MeSH term(s) Animals ; Breast Neoplasms/genetics ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Caenorhabditis elegans/genetics ; Caenorhabditis elegans/metabolism ; Cattle ; Chickens/genetics ; Chickens/metabolism ; Databases, Nucleic Acid ; Drosophila melanogaster/genetics ; Drosophila melanogaster/metabolism ; Female ; Genome ; Humans ; Male ; Mice ; MicroRNAs/classification ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Molecular Sequence Annotation ; Ovarian Neoplasms/genetics ; Ovarian Neoplasms/metabolism ; Ovarian Neoplasms/pathology ; Polymorphism, Single Nucleotide ; RNA, Long Noncoding/classification ; RNA, Long Noncoding/genetics ; RNA, Long Noncoding/metabolism ; RNA, Small Interfering/classification ; RNA, Small Interfering/genetics ; RNA, Small Interfering/metabolism ; Rats ; Species Specificity ; Uterine Cervical Neoplasms/genetics ; Uterine Cervical Neoplasms/metabolism ; Uterine Cervical Neoplasms/pathology ; Zebrafish/genetics ; Zebrafish/metabolism
    Chemical Substances MicroRNAs ; RNA, Long Noncoding ; RNA, Small Interfering
    Language English
    Publishing date 2020-10-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1555-8584
    ISSN (online) 1555-8584
    DOI 10.1080/15476286.2020.1833529
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Nur77 influences immunometabolism to regulate the release of proinflammatory cytokines and the formation of lipid bodies during Mycobacterium tuberculosis infection of macrophages.

    Birari, Pankaj / Mal, Soumya / Majumder, Debayan / Sharma, Arun K / Kumar, Manish / Das, Troyee / Ghosh, Zhumur / Jana, Kuladip / Gupta, Umesh D / Kundu, Manikuntala / Basu, Joyoti

    Pathogens and disease

    2023  Volume 81

    Abstract: Infection of macrophages with Mycobacterium tuberculosis induces innate immune responses designed to clear the invading bacterium. However, bacteria often survive within the intracellular environment by exploiting these responses triggered by macrophages. ...

    Abstract Infection of macrophages with Mycobacterium tuberculosis induces innate immune responses designed to clear the invading bacterium. However, bacteria often survive within the intracellular environment by exploiting these responses triggered by macrophages. Here, the role of the orphan nuclear receptor Nur77 (Nr4a1) in regulating the response of macrophages infected with M. tuberculosis (Mtb) has been delineated. Nur77 is induced early during infection, regulates metabolism by binding directly at the promoter of the TCA cycle enzyme, isocitrate dehydrogenase 2 (IDH2), to act as its repressor, and shifts the balance from a proinflammatory to an anti-inflammatory phenotype. Depletion of Nur77 increased transcription of IDH2 and, consequently, the levels of intracellular succinate, leading to enhanced levels of the proinflammatory cytokine IL-1β. Further, Nur77 inhibited the production of antibacterial nitric oxide and IL-1β in a succinate dehydrogenase (SDH)-dependent manner, suggesting that its induction favors bacterial survival by suppressing bactericidal responses. Indeed, depletion of Nur77 inhibited the intracellular survival of Mtb. On the other hand, depletion of Nur77 enhanced lipid body formation, suggesting that the fall in Nur77 levels as infection progresses likely favors foamy macrophage formation and long-term survival of Mtb in the host milieu.
    MeSH term(s) Humans ; Cytokines/metabolism ; Lipid Droplets/metabolism ; Macrophages ; Tuberculosis/microbiology ; Mycobacterium tuberculosis
    Chemical Substances Cytokines
    Language English
    Publishing date 2023-11-28
    Publishing country United States
    Document type Journal Article
    ISSN 2049-632X
    ISSN (online) 2049-632X
    DOI 10.1093/femspd/ftad033
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Repurposed drugs and nutraceuticals targeting envelope protein: A possible therapeutic strategy against COVID-19.

    Das, Gourab / Das, Troyee / Chowdhury, Nilkanta / Chatterjee, Durbadal / Bagchi, Angshuman / Ghosh, Zhumur

    Genomics

    2020  Volume 113, Issue 1 Pt 2, Page(s) 1129–1140

    Abstract: COVID-19 pandemic caused by SARS-CoV-2 has already claimed millions of lives worldwide due to the absence of a suitable anti-viral therapy. The CoV envelope (E) protein, which has not received much attention so far, is a 75 amino acid long integral ... ...

    Abstract COVID-19 pandemic caused by SARS-CoV-2 has already claimed millions of lives worldwide due to the absence of a suitable anti-viral therapy. The CoV envelope (E) protein, which has not received much attention so far, is a 75 amino acid long integral membrane protein involved in assembly and release of the virus inside the host. Here we have used artificial intelligence (AI) and pattern recognition techniques for initial screening of FDA approved pharmaceuticals and nutraceuticals to target this E protein. Subsequently, molecular docking simulations have been performed between the ligands and target protein to screen a set of 9 ligand molecules. Finally, we have provided detailed insight into their mechanisms of action related to the varied symptoms of infected patients.
    MeSH term(s) Antiviral Agents/therapeutic use ; Artificial Intelligence ; COVID-19/diet therapy ; COVID-19/virology ; Conserved Sequence ; Coronavirus Envelope Proteins/drug effects ; Coronavirus Envelope Proteins/genetics ; Dietary Supplements ; Drug Evaluation, Preclinical/methods ; Drug Repositioning ; Humans ; Machine Learning ; Models, Molecular ; Molecular Docking Simulation ; Pandemics ; Pattern Recognition, Automated ; SARS-CoV-2/chemistry ; SARS-CoV-2/drug effects ; SARS-CoV-2/genetics ; User-Computer Interface ; COVID-19 Drug Treatment
    Chemical Substances Antiviral Agents ; Coronavirus Envelope Proteins ; envelope protein, SARS-CoV-2
    Keywords covid19
    Language English
    Publishing date 2020-11-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 356334-0
    ISSN 1089-8646 ; 0888-7543
    ISSN (online) 1089-8646
    ISSN 0888-7543
    DOI 10.1016/j.ygeno.2020.11.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Honokiol, an inducer of sirtuin-3, protects against non-steroidal anti-inflammatory drug-induced gastric mucosal mitochondrial pathology, apoptosis and inflammatory tissue injury.

    Debsharma, Subhashis / Pramanik, Saikat / Bindu, Samik / Mazumder, Somnath / Das, Troyee / Saha, Debanjan / De, Rudranil / Nag, Shiladitya / Banerjee, Chinmoy / Siddiqui, Asim Azhar / Ghosh, Zhumur / Bandyopadhyay, Uday

    British journal of pharmacology

    2023  Volume 180, Issue 18, Page(s) 2317–2340

    Abstract: Background and purpose: Mitochondrial oxidative stress, inflammation and apoptosis primarily underlie gastric mucosal injury caused by the widely used non-steroidal anti-inflammatory drugs (NSAIDs). Alternative gastroprotective strategies are therefore ... ...

    Abstract Background and purpose: Mitochondrial oxidative stress, inflammation and apoptosis primarily underlie gastric mucosal injury caused by the widely used non-steroidal anti-inflammatory drugs (NSAIDs). Alternative gastroprotective strategies are therefore needed. Sirtuin-3 pivotally maintains mitochondrial structural integrity and metabolism while preventing oxidative stress; however, its relevance to gastric injury was never explored. Here, we have investigated whether and how sirtuin-3 stimulation by the phytochemical, honokiol, could rescue NSAID-induced gastric injury.
    Experimental approach: Gastric injury in rats induced by indomethacin was used to assess the effects of honokiol. Next-generation sequencing-based transcriptomics followed by functional validation identified the gastroprotective function of sirtuin-3. Flow cytometry, immunoblotting, qRT-PCR and immunohistochemistry were used measure effects on oxidative stress, mitochondrial dynamics, electron transport chain function, and markers of inflammation and apoptosis. Sirtuin-3 deacetylase activity was also estimated and gastric luminal pH was measured.
    Key results: Indomethacin down-regulated sirtuin-3 to induce oxidative stress, mitochondrial hyperacetylation, 8-oxoguanine DNA glycosylase 1 depletion, mitochondrial DNA damage, respiratory chain defect and mitochondrial fragmentation leading to severe mucosal injury. Indomethacin dose-dependently inhibited sirtuin-3 deacetylase activity. Honokiol prevented mitochondrial oxidative damage and inflammatory tissue injury by attenuating indomethacin-induced depletion of both sirtuin-3 and its transcriptional regulators PGC1α and ERRα. Honokiol also accelerated gastric wound healing but did not alter gastric acid secretion, unlike lansoprazole.
    Conclusions and implications: Sirtuin-3 stimulation by honokiol prevented and reversed NSAID-induced gastric injury through maintaining mitochondrial integrity. Honokiol did not affect gastric acid secretion. Sirtuin-3 stimulation by honokiol may be utilized as a mitochondria-based, acid-independent novel gastroprotective strategy against NSAIDs.
    MeSH term(s) Rats ; Animals ; Sirtuin 3/metabolism ; Rats, Sprague-Dawley ; Anti-Inflammatory Agents, Non-Steroidal/pharmacology ; Indomethacin/toxicity ; Gastric Mucosa/metabolism ; Apoptosis ; Inflammation/metabolism
    Chemical Substances honokiol (11513CCO0N) ; Sirtuin 3 (EC 3.5.1.-) ; Anti-Inflammatory Agents, Non-Steroidal ; Indomethacin (XXE1CET956)
    Language English
    Publishing date 2023-05-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80081-8
    ISSN 1476-5381 ; 0007-1188
    ISSN (online) 1476-5381
    ISSN 0007-1188
    DOI 10.1111/bph.16070
    Database MEDical Literature Analysis and Retrieval System OnLINE

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