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  1. Article ; Online: Silicon p-i-n junction fibers.

    He, Rongrui / Day, Todd D / Krishnamurthi, Mahesh / Sparks, Justin R / Sazio, Pier J A / Gopalan, Venkatraman / Badding, John V

    Advanced materials (Deerfield Beach, Fla.)

    2012  Volume 25, Issue 10, Page(s) 1461–1467

    Abstract: Flexible Si p-i-n junction fibers made by high pressure chemical vapor deposition offer new ...

    Abstract Flexible Si p-i-n junction fibers made by high pressure chemical vapor deposition offer new opportunities in textile photovoltaics and optoelectronics, as exemplified by their photovoltaic properties, gigahertz bandwidth for photodetection, and ability to waveguide light.
    Language English
    Publishing date 2012-12-04
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1474949-X
    ISSN 1521-4095 ; 0935-9648
    ISSN (online) 1521-4095
    ISSN 0935-9648
    DOI 10.1002/adma.201203879
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Menadione (vitamin K3) inhibits hydrogen sulfide and substance P via NF-кB pathway in caerulein-induced acute pancreatitis and associated lung injury in mice.

    Amiti / Tamizhselvi, Ramasamy / Manickam, Venkatraman

    Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.

    2019  Volume 19, Issue 2, Page(s) 266–273

    Abstract: ... intraperitoneal (i.p) injections of caerulein (50 μg/kg at 1 h interval). Menadione (10 mg/kg) was administered ... one hour (i.p, 10 mg/kg) after the first caerulein injection and control animals were given hourly ... intraperitoneal (i.p) injection of isotonic sodium chloride solution for 6 hours.: Results: Administration ...

    Abstract Objective: We aim to study the protective effect of menadione on caerulein-induced acute pancreatitis (AP) and associated lung injury and to explore the possible mechanism.
    Methods: Male Swiss mice randomized into control and different experimental groups. AP was induced in mice by six hourly intraperitoneal (i.p) injections of caerulein (50 μg/kg at 1 h interval). Menadione (10 mg/kg) was administered one hour (i.p, 10 mg/kg) after the first caerulein injection and control animals were given hourly intraperitoneal (i.p) injection of isotonic sodium chloride solution for 6 hours.
    Results: Administration of menadione attenuated the severity of AP and associated lung injury as shown by the histopathology, reduced MPO and serum amylase activity. Further, the anti-inflammatory effect of menadione was associated with a reduction of pancreatic and pulmonary proinflammatory cytokine interleukin 1β (IL-1β) and hydrogen sulfide (H
    Conclusion: The present findings show for the first time that in AP, menadione may exhibit an anti-inflammatory effect by down-regulating substance-P and H
    MeSH term(s) Amylases ; Animals ; Ceruletide/toxicity ; Gene Expression Regulation/drug effects ; Hydrogen Sulfide/metabolism ; Interleukin-1beta/genetics ; Interleukin-1beta/metabolism ; Lung Injury/etiology ; Lung Injury/prevention & control ; Male ; Mice ; NF-kappa B/metabolism ; Pancreatitis/chemically induced ; Pancreatitis/complications ; Peroxidase/metabolism ; Random Allocation ; Substance P/metabolism ; Vitamin K 3/pharmacology
    Chemical Substances Interleukin-1beta ; NF-kappa B ; Substance P (33507-63-0) ; Vitamin K 3 (723JX6CXY5) ; Ceruletide (888Y08971B) ; Peroxidase (EC 1.11.1.7) ; Amylases (EC 3.2.1.-) ; Hydrogen Sulfide (YY9FVM7NSN)
    Language English
    Publishing date 2019-01-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2056680-3
    ISSN 1424-3911 ; 1424-3903
    ISSN (online) 1424-3911
    ISSN 1424-3903
    DOI 10.1016/j.pan.2019.01.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Demonstration of the Blood-Stage Plasmodium falciparum Controlled Human Malaria Infection Model to Assess Efficacy of the P. falciparum Apical Membrane Antigen 1 Vaccine, FMP2.1/AS01.

    Payne, Ruth O / Milne, Kathryn H / Elias, Sean C / Edwards, Nick J / Douglas, Alexander D / Brown, Rebecca E / Silk, Sarah E / Biswas, Sumi / Miura, Kazutoyo / Roberts, Rachel / Rampling, Thomas W / Venkatraman, Navin / Hodgson, Susanne H / Labbé, Geneviève M / Halstead, Fenella D / Poulton, Ian D / Nugent, Fay L / de Graaf, Hans / Sukhtankar, Priya /
    Williams, Nicola C / Ockenhouse, Christian F / Kathcart, April K / Qabar, Aziz N / Waters, Norman C / Soisson, Lorraine A / Birkett, Ashley J / Cooke, Graham S / Faust, Saul N / Woods, Colleen / Ivinson, Karen / McCarthy, James S / Diggs, Carter L / Vekemans, Johan / Long, Carole A / Hill, Adrian V S / Lawrie, Alison M / Dutta, Sheetij / Draper, Simon J

    The Journal of infectious diseases

    2016  Volume 213, Issue 11, Page(s) 1743–1751

    Abstract: ... of a blood-stage P. falciparum CHMI model to assess blood-stage vaccine candidates, using their impact ... growth inhibitory activity against P. falciparum in vitro. There were no vaccine- or CHMI-related safety concerns ...

    Abstract Background: Models of controlled human malaria infection (CHMI) initiated by mosquito bite have been widely used to assess efficacy of preerythrocytic vaccine candidates in small proof-of-concept phase 2a clinical trials. Efficacy testing of blood-stage malaria parasite vaccines, however, has generally relied on larger-scale phase 2b field trials in malaria-endemic populations. We report the use of a blood-stage P. falciparum CHMI model to assess blood-stage vaccine candidates, using their impact on the parasite multiplication rate (PMR) as the primary efficacy end point.
    Methods: Fifteen healthy United Kingdom adult volunteers were vaccinated with FMP2.1, a protein vaccine that is based on the 3D7 clone sequence of apical membrane antigen 1 (AMA1) and formulated in Adjuvant System 01 (AS01). Twelve vaccinees and 15 infectivity controls subsequently underwent blood-stage CHMI. Parasitemia was monitored by quantitative real-time polymerase chain reaction (PCR) analysis, and PMR was modeled from these data.
    Results: FMP2.1/AS01 elicited anti-AMA1 T-cell and serum antibody responses. Analysis of purified immunoglobulin G showed functional growth inhibitory activity against P. falciparum in vitro. There were no vaccine- or CHMI-related safety concerns. All volunteers developed blood-stage parasitemia, with no impact of the vaccine on PMR.
    Conclusions: FMP2.1/AS01 demonstrated no efficacy after blood-stage CHMI. However, the model induced highly reproducible infection in all volunteers and will accelerate proof-of-concept testing of future blood-stage vaccine candidates.
    Clinical trials registration: NCT02044198.
    MeSH term(s) Adult ; Antigens, Protozoan/immunology ; Enzyme-Linked Immunospot Assay ; Erythrocytes/parasitology ; Female ; Humans ; Immunogenicity, Vaccine ; Life Cycle Stages ; Malaria Vaccines/immunology ; Malaria, Falciparum/parasitology ; Malaria, Falciparum/prevention & control ; Male ; Membrane Proteins/immunology ; Middle Aged ; Models, Biological ; Plasmodium falciparum/immunology ; Plasmodium falciparum/physiology ; Protozoan Proteins/immunology ; Young Adult
    Chemical Substances Antigens, Protozoan ; Malaria Vaccines ; Membrane Proteins ; Protozoan Proteins ; apical membrane antigen I, Plasmodium
    Language English
    Publishing date 2016-02-04
    Publishing country United States
    Document type Clinical Trial ; Journal Article
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiw039
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Zinc finger nuclease-mediated gene knockout results in loss of transport activity for P-glycoprotein, BCRP, and MRP2 in Caco-2 cells.

    Sampson, Kathleen E / Brinker, Amanda / Pratt, Jennifer / Venkatraman, Neetu / Xiao, Yongling / Blasberg, Jim / Steiner, Toni / Bourner, Maureen / Thompson, David C

    Drug metabolism and disposition: the biological fate of chemicals

    2015  Volume 43, Issue 2, Page(s) 199–207

    Abstract: Membrane transporters P-glycoprotein [P-gp; multidrug resistance 1 (MDR1 ... or 10 μM for 2 hours at 37°C. P-gp substrates digoxin and erythromycin, BCRP substrates estrone 3 ...

    Abstract Membrane transporters P-glycoprotein [P-gp; multidrug resistance 1 (MDR1)], multidrug resistance-associated protein (MRP) 2, and breast cancer resistance protein (BCRP) affect drug absorption and disposition and can also mediate drug-drug interactions leading to safety/toxicity concerns in the clinic. Challenges arise with interpreting cell-based transporter assays when substrates or inhibitors affect more than one actively expressed transporter and when endogenous or residual transporter activity remains following overexpression or knockdown of a given transporter. The objective of this study was to selectively knock out three drug efflux transporter genes (MDR1, MRP2, and BCRP), both individually as well as in combination, in a subclone of Caco-2 cells (C2BBe1) using zinc finger nuclease technology. The wild-type parent and knockout cell lines were tested for transporter function in Transwell bidirectional assays using probe substrates at 5 or 10 μM for 2 hours at 37°C. P-gp substrates digoxin and erythromycin, BCRP substrates estrone 3-sulfate and nitrofurantoin, and MRP2 substrate 5-(and-6)-carboxy-2',7'-dichlorofluorescein each showed a loss of asymmetric transport in the MDR1, BCRP, and MRP2 knockout cell lines, respectively. Furthermore, transporter interactions were deduced for cimetidine, ranitidine, fexofenadine, and colchicine. Compared with the knockout cell lines, standard transporter inhibitors showed substrate-specific variation in reducing the efflux ratios of the test compounds. These data confirm the generation of a panel of stable Caco-2 cell lines with single or double knockout of human efflux transporter genes and a complete loss of specific transport activity. These cell lines may prove useful in clarifying complex drug-transporter interactions without some of the limitations of current chemical or genetic knockdown approaches.
    MeSH term(s) ATP Binding Cassette Transporter, Sub-Family B/antagonists & inhibitors ; ATP Binding Cassette Transporter, Sub-Family B/genetics ; ATP Binding Cassette Transporter, Sub-Family B/metabolism ; ATP Binding Cassette Transporter, Sub-Family G, Member 2 ; ATP-Binding Cassette Transporters/antagonists & inhibitors ; ATP-Binding Cassette Transporters/genetics ; ATP-Binding Cassette Transporters/metabolism ; Biological Transport/drug effects ; Caco-2 Cells ; Cell Membrane Permeability/drug effects ; Clone Cells ; Drug Evaluation, Preclinical/methods ; Drug Interactions ; Enterocytes/drug effects ; Enterocytes/metabolism ; Gene Knockout Techniques ; Humans ; Multidrug Resistance-Associated Proteins/antagonists & inhibitors ; Multidrug Resistance-Associated Proteins/genetics ; Multidrug Resistance-Associated Proteins/metabolism ; Neoplasm Proteins/antagonists & inhibitors ; Neoplasm Proteins/genetics ; Neoplasm Proteins/metabolism ; RNA, Messenger/metabolism ; Xenobiotics/analysis ; Xenobiotics/metabolism ; Xenobiotics/pharmacology
    Chemical Substances ABCB1 protein, human ; ABCG2 protein, human ; ATP Binding Cassette Transporter, Sub-Family B ; ATP Binding Cassette Transporter, Sub-Family G, Member 2 ; Multidrug Resistance-Associated Proteins ; Neoplasm Proteins ; RNA, Messenger ; Xenobiotics ; multidrug resistance-associated protein 2 (4AF605U6JN)
    Language English
    Publishing date 2015-02
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 186795-7
    ISSN 1521-009X ; 0090-9556
    ISSN (online) 1521-009X
    ISSN 0090-9556
    DOI 10.1124/dmd.114.057216
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Central and peripheral contrast sensitivity in thyroid eye disease.

    Bhattacharjee, Kasturi / Rehman, Obaidur / Ichhpujani, Parul / Venkatraman, Vatsalya

    Indian journal of ophthalmology

    2024  

    Abstract: ... patients and controls was statistically insignificant (P = 0.189), but a significant difference was noted ... in central and total CS score (P < 0.001, Wilcoxon-Mann-Whitney test). On CS comparison between DON and non ... DON eyes, a significant difference in average scores was noted in central and all peripheral areas (P ...

    Abstract Purpose: Assessment of central and peripheral contrast sensitivity (CS) in thyroid eye disease (TED) with and without dysthyroid optic neuropathy (DON).
    Methods: This cross-sectional study enrolled 33 eyes of 18 treatment-naïve TED patients and 18 age- and sex-matched healthy controls for comparative analysis. A detailed ophthalmic examination included visual acuity (VA), intraocular pressure measurement, slit-lamp biomicroscopy, and CS testing (central and four peripheral regions) using Spaeth-Richman Contrast Sensitivity test was done.
    Results: The average age of TED patients was 47.17 ± 13.99 years and a female preponderance was noted (66.66%, n = 12). Twenty-five eyes (75.8%) were diagnosed as TED without DON, while eight eyes (24.2%) had DON. Nine eyes (27.2%) were in the active stage of disease and 29 eyes (87.8%) had proptosis. The difference in mean logMAR visual acuities between TED patients and controls was statistically insignificant (P = 0.189), but a significant difference was noted in central and total CS score (P < 0.001, Wilcoxon-Mann-Whitney test). On CS comparison between DON and non-DON eyes, a significant difference in average scores was noted in central and all peripheral areas (P < 0.05, Wilcoxon-Mann-Whitney test). With increasing clinical activity score, a statistically significant reduction was noted in CS in three out of four peripheral regions (Spearman correlation, P < 0.05).
    Conclusion: Visual function compromise can be detected in TED in the presence of intact VA, by testing CS. Peripheral CS deteriorates with increasing inflammation and in DON. Serial monitoring of both central and peripheral CS may help in diagnosing DON early.
    Language English
    Publishing date 2024-04-16
    Publishing country India
    Document type Journal Article
    ZDB-ID 187392-1
    ISSN 1998-3689 ; 0301-4738
    ISSN (online) 1998-3689
    ISSN 0301-4738
    DOI 10.4103/IJO.IJO_2593_23
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  6. Article ; Online: Subsume Pediatric Headaches in Psychiatric Disorders? Critiques on Delphic Nosology, Diagnostic Conundrums, and Variability in the Interventions.

    Sharma, Aditya / Khurana, Priyal / Venkatraman, Akila / Gupta, Mayank

    Current pain and headache reports

    2024  

    Abstract: Purpose of review: Tension-type headache (TTH) continues to be the most prevalent type of headache across all age groups worldwide, and the global burden of migraine and TTH together account for 7% of all-cause years lived with disability (YLDs). TTH ... ...

    Abstract Purpose of review: Tension-type headache (TTH) continues to be the most prevalent type of headache across all age groups worldwide, and the global burden of migraine and TTH together account for 7% of all-cause years lived with disability (YLDs). TTH has been shown to have a prevalence of up to 80% in several studies and presents a wide range and high variability in clinical settings. The aim of this review is to identify gaps in diagnostics, nosology, and variability in the treatment of children and adolescents who present with headaches without an identifiable etiology.
    Recent findings: Migraine and TTH have been debated to have more similarities than distinctions, increasing chances of misdiagnosis and leading to significant cases diagnosed as probable TTH or probable migraine. The lack of specificity and sensitivity for TTH classification often leads to the diagnosis being made by negating associated migraine symptoms. Although pathology is not well understood, some studies have suggested a neurological basis for TTH, in need of further validation. Some research indicates that nitric oxide signaling plays an integral part in the pain mechanisms related to TTH. Analgesics and non-steroidal anti-inflammatories are usually the first lines of treatment for children with recurring headaches, and additional treatment options include medication and behavioral therapies. With high prevalence and socioeconomic burden among children and adolescents, it's essential to further study Tension-type headaches and secondary headaches without known cause and potential interventions. Treatment studies involving randomized controlled trials are also needed to test the efficacy of various treatments further.
    Language English
    Publishing date 2024-02-17
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2055062-5
    ISSN 1534-3081 ; 1531-3433
    ISSN (online) 1534-3081
    ISSN 1531-3433
    DOI 10.1007/s11916-024-01225-7
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  7. Article ; Online: A cross talk study on sitagliptin mediated reclamation on TGF β signalling, DPP 4, miR-29a and miR-24 expression in PCOS rats fed with high fat-high fructose diet.

    Nanda, Dipti / Venkatraman, Anuradha Carani / Kalaivanan, Kalpana

    Tissue & cell

    2024  Volume 88, Page(s) 102375

    Abstract: ... testosterone propionate (TP) for 28 days to both the CD/HFFD rats and treated with STG i.p. for last 15 days. At the end ... κB-p65, TGF-β1, p-Smad 2 and p-Smad 3 followed by no significant changes in the expression of BAX ...

    Abstract Polycystic Ovary Syndrome (PCOS) is a multifactorial reproductive, endocrine and metabolic disturbance which is very commonly observed in females of reproductive age group. The disease is still incurable however the use of synthetic drugs in combination with lifestyle is recommended. Accordingly, the present study was conducted to investigate the possible beneficial effects of sitagliptin on PCOS induced rats on control diet (CD)/high fat- high fructose diet (HFFD). PCOS was induced by giving testosterone propionate (TP) for 28 days to both the CD/HFFD rats and treated with STG i.p. for last 15 days. At the end of the experiment lipid profile, inflammatory markers, expression of NF-κB-p65, miR-24 and miR-29a, fibrotic and apoptotic proteins from ovary tissue were examined. Moreover, lipid accumulation and fibrosis of ovary tissue was further confirmed using Sudan III and Masson's trichrome stain. STG treated rats exerted a significant decrease in levels of cholesterol, TG, LDL-C, VLDL-C, IL-6 and TNF-α and increased HDL-C level, miR-24 and miR-29a expression. STG treated groups expressed significantly decreased expression of NF-κB-p65, TGF-β1, p-Smad 2 and p-Smad 3 followed by no significant changes in the expression of BAX, caspase-9, caspase-3 and Bcl-2 in all the PCOS induced groups. Among all the CD/ HFFD fed groups, rats on HFFD showed more devastating effect which suggests that diet plays a major role in genesis of PCOS. In conclusion, current results reflect the potential impact of STG against dyslipidaemia, inflammation and fibrosis in PCOS rats via regulating dyslipidaemia and fibrosis via DPP 4 mediated miR-29a expression.
    Language English
    Publishing date 2024-04-04
    Publishing country Scotland
    Document type Journal Article
    ZDB-ID 204424-9
    ISSN 1532-3072 ; 0040-8166
    ISSN (online) 1532-3072
    ISSN 0040-8166
    DOI 10.1016/j.tice.2024.102375
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  8. Article ; Online: Predicting sensitivity of non-small-cell lung cancer to gefitinib: is there a role for P-Akt?

    Pao, William / Miller, Vincent A / Venkatraman, Ennapadam / Kris, Mark G

    Journal of the National Cancer Institute

    2004  Volume 96, Issue 15, Page(s) 1117–1119

    MeSH term(s) Antineoplastic Agents/pharmacology ; Antineoplastic Agents/therapeutic use ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/metabolism ; Enzyme Inhibitors/therapeutic use ; Gene Expression Regulation, Neoplastic/drug effects ; Humans ; Lung Neoplasms/drug therapy ; Lung Neoplasms/metabolism ; Mitogen-Activated Protein Kinase Kinases/drug effects ; Mitogen-Activated Protein Kinase Kinases/metabolism ; Predictive Value of Tests ; Prognosis ; Protein-Serine-Threonine Kinases/drug effects ; Protein-Serine-Threonine Kinases/metabolism ; Protein-Tyrosine Kinases/antagonists & inhibitors ; Protein-Tyrosine Kinases/metabolism ; Proto-Oncogene Proteins/drug effects ; Proto-Oncogene Proteins/metabolism ; Proto-Oncogene Proteins c-akt ; Quinazolines/pharmacology ; Quinazolines/therapeutic use ; Receptor, Epidermal Growth Factor/drug effects ; Receptor, Epidermal Growth Factor/metabolism ; Treatment Outcome
    Chemical Substances Antineoplastic Agents ; Enzyme Inhibitors ; Proto-Oncogene Proteins ; Quinazolines ; Protein-Tyrosine Kinases (EC 2.7.10.1) ; Receptor, Epidermal Growth Factor (EC 2.7.10.1) ; AKT1 protein, human (EC 2.7.11.1) ; Protein-Serine-Threonine Kinases (EC 2.7.11.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; Mitogen-Activated Protein Kinase Kinases (EC 2.7.12.2) ; gefitinib (S65743JHBS)
    Language English
    Publishing date 2004-08-04
    Publishing country United States
    Document type Comment ; Editorial
    ZDB-ID 2992-0
    ISSN 1460-2105 ; 0027-8874 ; 0198-0157
    ISSN (online) 1460-2105
    ISSN 0027-8874 ; 0198-0157
    DOI 10.1093/jnci/djh244
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  9. Article ; Online: Novel Nexus with NFκB, β-catenin, and RB1 empowers PSMD10/Gankyrin to counteract TNF-α induced apoptosis establishing its oncogenic role.

    Mulla, Saim Wasi / Venkatraman, Prasanna

    The international journal of biochemistry & cell biology

    2022  Volume 146, Page(s) 106209

    Abstract: NFκB is a critical rapid-acting transcription factor that protects cancer cells from programmed cell death induced by stress or therapy. While NFκB works in nexus with non-classical oncoproteins such as STAT3 and AKT under a variety of conditions, it is ... ...

    Abstract NFκB is a critical rapid-acting transcription factor that protects cancer cells from programmed cell death induced by stress or therapy. While NFκB works in nexus with non-classical oncoproteins such as STAT3 and AKT under a variety of conditions, it is a major antiapoptotic factor activated by TNF-α of the tumor microenvironment. Therefore, it is surprising that PSMD10, an oncoprotein overexpressed in several cancers and a marker of poor prognosis, is reported to inhibit the NFκB pathway. In this study, we explore the role of PSMD10 in cancer cells exposed to TNF-α. We screen several breast and colon cancer cell lines and select SW480, a colon cancer cell line highly resistant to TNF-α, and demonstrate that PSMD10 knockdown sensitizes these cells to TNF-α induced cell death. One of the mechanisms involves transcriptional regulation of β-catenin and RB1, two key colon cancer cell specific anti-apoptotic factors. Surprisingly, we find that PSMD10 is required for optimal phosphorylation and transcriptional activation of NFκB (RELA). Thus, upon PSMD10 knockdown, there is significant downregulation of anti-apoptotic NFκB target genes TNFAIP3 (A20), BIRC2 (cIAP1), BIRC3 (cIAP2), and XIAP. Our study, for the first time, shows that PSMD10 is required for the activation of the pro-survival arm via NFκB transcriptional activation to prevent cancer cells from succumbing to TNF-induced cell death. In addition by transcriptional regulation of two major antiapoptotic players RB1 and β-catenin, PSMD10 proves to be a coveted oncoprotein with a key role in tumorigenesis.
    MeSH term(s) Apoptosis ; Carcinogenesis ; Cell Line, Tumor ; Colonic Neoplasms ; Humans ; NF-kappa B/metabolism ; Proteasome Endopeptidase Complex/metabolism ; Proto-Oncogene Proteins/metabolism ; Retinoblastoma Binding Proteins/metabolism ; Tumor Microenvironment ; Tumor Necrosis Factor-alpha/metabolism ; Tumor Necrosis Factor-alpha/pharmacology ; Ubiquitin-Protein Ligases/genetics ; Ubiquitin-Protein Ligases/metabolism ; beta Catenin/genetics ; beta Catenin/metabolism
    Chemical Substances NF-kappa B ; PSMD10 protein, human ; Proto-Oncogene Proteins ; RB1 protein, human ; Retinoblastoma Binding Proteins ; Tumor Necrosis Factor-alpha ; beta Catenin ; Ubiquitin-Protein Ligases (EC 2.3.2.27) ; Proteasome Endopeptidase Complex (EC 3.4.25.1)
    Language English
    Publishing date 2022-04-02
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1228429-4
    ISSN 1878-5875 ; 1357-2725
    ISSN (online) 1878-5875
    ISSN 1357-2725
    DOI 10.1016/j.biocel.2022.106209
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  10. Article ; Online: Investigating radiation profiles and conducting risk assessment for ecological and environmental components on Vaan and Koswari islands in the Tuticorin group of islands, India.

    Krishnan, S J Athul / Nishanth, P / Venkatraman, Atvr / Krishnakumar, S / Priyadharshini, Marckasagayam / Musthafa, Mohamed Saiyad

    Environmental monitoring and assessment

    2024  Volume 196, Issue 2, Page(s) 139

    Abstract: Natural radioactive concentration assessment was conducted on sediment, water, and biota obtained on Vaan and Koswari islands in the Tuticorin group of islands, Tamil Nadu, India. For biotic and abiotic components, radiation profiles such as gross alpha, ...

    Abstract Natural radioactive concentration assessment was conducted on sediment, water, and biota obtained on Vaan and Koswari islands in the Tuticorin group of islands, Tamil Nadu, India. For biotic and abiotic components, radiation profiles such as gross alpha, beta, primordial radionuclide, polonium, and lead analyses were performed. The gross α and β range from BDL to 15.18 ± 1.7 Bq/kg and 40.43 ± 4.9 Bq/kg to 105.12 ± 11.7 Bq/kg, respectively. Primordial radionuclides were analyzed using Nal(TI)-based scintillator with PC-MCA, and the concentrations ranged from 13.43 ± 3.3 Bq/kg to 30.97 ± 9.6 Bq/kg with a mean of 21.31 ± 2.7 Bq/kg for
    MeSH term(s) India ; Lead ; Environmental Monitoring ; Risk Assessment ; Water
    Chemical Substances Lead (2P299V784P) ; Water (059QF0KO0R)
    Language English
    Publishing date 2024-01-11
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 782621-7
    ISSN 1573-2959 ; 0167-6369
    ISSN (online) 1573-2959
    ISSN 0167-6369
    DOI 10.1007/s10661-024-12312-y
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