7 results on '"Madhry D"'
Search Results
2. Comprehensive Analysis of Juvenile Nasopharyngeal Angiofibromas via Whole-Exome Sequencing.
- Author
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Kumari K, Afroj S, Madhry D, Verma Y, Kairo AK, Thakar A, Sikka K, Verma H, and Verma B
- Subjects
- Humans, Male, Adolescent, Child, Ubiquitin Thiolesterase genetics, Angiofibroma genetics, Angiofibroma pathology, Exome Sequencing methods, Nasopharyngeal Neoplasms genetics, Nasopharyngeal Neoplasms pathology, Mutation
- Abstract
Introduction: The molecular basis and mechanisms of juvenile nasopharyngeal angiofibromas (JNA) pathogenesis are still unknown. Despite being a rare and benign neoplasm, JNA is a locally aggressive and potentially destructive head and neck neoplasm, typically found in young males. The advancement of genome technologies and analytical tools has provided an unparalleled opportunity to explore the intricacy of JNA. The present study provides the first evidence of the involvement of Y-chromosome genes in JNA., Methods: A total of 13 JNA patients at an advanced disease stage and five age-matched male controls were registered for this study. Whole-exome sequencing (WES) analysis was conducted followed by functional analysis to understand the molecular mechanism of the JNA., Results: WES analysis revealed a high prevalence of mutations in 14 genes within the protein-coding, male-specific region of the Y-chromosome of young males (mean age: 13.8 ± 2.4) with JNA. These mutations, occurring at 28 distinct positions, were characterized as moderate to high impact and were prevalent in nine JNA patients but not in the control group. The most frequently mutated genes were USP9Y and UTY, followed by KDM5D, DDX3Y, and TSPY4. The expression of USP9Y, UTY, and DDX3Y was found to be co-modulated, implying their coordinated regulation as a complex. Furthermore, somatic mutations were detected in genes previously linked to JNA., Conclusion: The wide array of genetic mutations in the Y-chromosome male-specific region, along with the somatic alterations identified in JNA, provides novel insights into JNA pathophysiology., (© 2024 Wiley Periodicals LLC.)
- Published
- 2024
- Full Text
- View/download PDF
3. Unravelling tRNA fragments in DENV pathogenesis: Insights from RNA sequencing.
- Author
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Madhry D, Kumari K, Meena V, Roy R, and Verma B
- Subjects
- Humans, Gene Expression Profiling methods, RNA, Transfer genetics, RNA, Transfer metabolism, Dengue Virus genetics, Dengue Virus pathogenicity, Sequence Analysis, RNA, Dengue virology, Dengue genetics, RNA, Small Untranslated genetics
- Abstract
Small non-coding RNAs (sncRNAs) derived from tRNAs are known as tRNA-derived small RNAs (tsRNAs). These tsRNAs are further categorized into tRNA-derived fragments (tRFs) and tRNA halves (tiRNAs), which play significant roles in the various molecular mechanisms underlying certain human diseases. However, the generation of tsRNAs and their potential roles during Dengue virus (DENV) infection is not yet known. Here, we performed small RNA sequencing to identify the generation and alterations in tsRNAs expression profiles of DENV-infected Huh7 cells. Upon DENV infection, tRNA fragmentation was found to be increased. We identified a significant number of differentially expressed tsRNAs during DENV infection. Interestingly, the 3'tRF population showed upregulation, while the i-tRF population exhibited downregulation. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was performed to analyze the impact of differentially expressed tsRNAs on DENV pathogenesis. Our results suggest that differentially expressed tsRNAs are involved in transcriptional regulation via RNA polymerase II promoter and metabolic pathways. Overall, our study contributes significantly to our understanding of the roles played by tsRNAs in the complex dynamics of DENV infection., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
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4. Synergistic correlation between host angiogenin and dengue virus replication.
- Author
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Madhry D, Malvankar S, Phadnis S, Srivastava RK, Bhattacharyya S, and Verma B
- Subjects
- Humans, Ribonuclease, Pancreatic genetics, Virus Replication, Ivermectin pharmacology, Dengue
- Abstract
DENV infection poses a major health concern globally and the pathophysiology relies heavily on host-cellular machinery. Although virus replication relies heavily on the host, the mechanistic details of DENV-host interaction is not fully characterized yet. Here, we are focusing on characterizing the mechanistic basis of virus-induced stress on the host cell. Specifically, we aim to characterize the role of the stress modulator ribonuclease Angiogenin during DENV infection. Our results suggested that the levels of Angiogenin are up-regulated in DENV-infected cells and the levels increase proportionately with DENV replication. Our efforts to knockdown Angiogenin using siRNA were unsuccessful in DENV-infected cells but not in mock-infected control. To further investigate the modulation between DENV replication and Angiogenin, we treated Huh7 cells with Ivermectin prior to DENV infection. Our results suggest a significant reduction in DENV replication specifically at the later stages as a consequence of Ivermectin treatment. Interestingly, Angiogenin levels were also found to be decreased proportionately. Our results suggest that Angiogenin modulation during DENV infection is important for DENV replication and pathogenesis.
- Published
- 2023
- Full Text
- View/download PDF
5. Regulatory roles of tRNA-derived RNA fragments in human pathophysiology.
- Author
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Pandey KK, Madhry D, Ravi Kumar YS, Malvankar S, Sapra L, Srivastava RK, Bhattacharyya S, and Verma B
- Abstract
Hundreds of tRNA genes and pseudogenes are encoded by the human genome. tRNAs are the second most abundant type of RNA in the cell. Advancement in deep-sequencing technologies have revealed the presence of abundant expression of functional tRNA-derived RNA fragments (tRFs). They are either generated from precursor (pre-)tRNA or mature tRNA. They have been found to play crucial regulatory roles during different pathological conditions. Herein, we briefly summarize the discovery and recent advances in deciphering the regulatory role played by tRFs in the pathophysiology of different human diseases., Competing Interests: The authors declare no competing interests., (© 2021 The Author(s).)
- Published
- 2021
- Full Text
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6. Role of non-coding RNAs in Dengue virus-host interaction.
- Author
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Madhry D, Pandey KK, Kaur J, Rawat Y, Sapra L, Y S RK, Srivastava RK, Bhattacharyya S, and Verma B
- Subjects
- Animals, Humans, Dengue Virus genetics, RNA, Untranslated genetics, RNA, Viral genetics
- Abstract
Dengue is potentially a life-threatening arthropod-borne viral infection for which there are no known therapeutic agents till date. Early stage diagnosis of dengue infection is still lacking. Diagnosis is only made after severe manifestations and later stages of infection. Timely prognosis can prevent dengue related mortalities. The nucleic acid-based therapy has potential to emerge as a promising approach for early diagnosis and treatment of this viral infection. Many studies have been carried out suggested the regulatory role of ncRNAs thereby revealing the importance of protein-RNA and RNA-RNA interactions during infection. Various regulatory RNAs are either expressed by mammalian cells or generated by viral RNA have reported to play important roles in viral life cycle including dengue virus. Thus exploring host-virus interaction will pave the novel path for understanding the pathophysiology of febrile infection in dengue. Rapid advances in sequencing techniques along with significant developments in the field of RNA studies has made RNA therapeutics as one of the promising approaches as antiviral targets. The idea of RNA based therapies has been greatly backed by a Hepatitis C virus drug, Miravirsen which has successfully completed phase II clinical trial. In the present review, we will discuss the implications of different non-coding RNAs in dengue infection. Differential expression of small ncRNA may serve as a reliable biomarker of disease severity during different stages of infection and can also play regulatory roles in disease progression., (© 2021 The Author(s). Published by BRI.)
- Published
- 2021
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7. Phytotherapy for treatment of cytokine storm in COVID-19.
- Author
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Sapra L, Bhardwaj A, Azam Z, Madhry D, Verma B, Rathore S, and Srivastava RK
- Subjects
- COVID-19 immunology, COVID-19 virology, Cytokine Release Syndrome immunology, Cytokines immunology, Cytokines metabolism, Humans, Macrophages drug effects, Macrophages immunology, Macrophages metabolism, Plants, Medicinal classification, SARS-CoV-2 immunology, SARS-CoV-2 pathogenicity, Virulence drug effects, Virulence immunology, Cytokine Release Syndrome prevention & control, Phytotherapy methods, Plant Extracts therapeutic use, Plants, Medicinal chemistry, SARS-CoV-2 drug effects, COVID-19 Drug Treatment
- Abstract
In 2020, a novel strain of coronavirus (COVID-19) has led to a significant morbidity and mortality worldwide. As of the date of this writing, a total of 116 M cases has been diagnosed worldwide leading to 2.5 M deaths. The number of mortalities is directly correlated with the rise of innate immune cells (especially macrophages) in the lungs that secrete inflammatory cytokines (IL-1β and IL-6) leading to the development of "Cytokine Storm Syndrome" (CSS), multi-organ-failure and death. Given that currently the treatment of this condition is rare and release of effective vaccine might be months away, here, we review the plants and their pharmacologically active-compounds as potential phytopharmaceuticals for the virus induced inflammatory response. Experimental validation of the effectiveness of these natural compounds to prevent or reduce the cytokine storm might be beneficial as an adjunct treatment of SARS-CoV-2., (© 2021 The Author(s). Published by BRI.)
- Published
- 2021
- Full Text
- View/download PDF
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