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  1. Article ; Online: Developmental and foliation changes due to dysregulation of adenosine kinase in the cerebellum.

    Gebril, Hoda M / Lai, Tho / Fedele, Denise E / Wahba, Amir

    Scientific reports

    2023  Volume 13, Issue 1, Page(s) 19831

    Abstract: Adenosine kinase (ADK), the major adenosine-metabolizing enzyme, plays a key role in brain development and disease. In humans, mutations in the Adk gene have been linked to developmental delay, stunted growth, and intellectual disability. To better ... ...

    Abstract Adenosine kinase (ADK), the major adenosine-metabolizing enzyme, plays a key role in brain development and disease. In humans, mutations in the Adk gene have been linked to developmental delay, stunted growth, and intellectual disability. To better understand the role of ADK in brain development, it is important to dissect the specific roles of the two isoforms of the enzyme expressed in the cytoplasm (ADK-S) and cell nucleus (ADK-L). We, therefore, studied brain development in Adk-tg transgenic mice, which only express ADK-S in the absence of ADK-L throughout development. In the mutant animals, we found a reduction in the overall brain, body size, and weight during fetal and postnatal development. As a major developmental abnormality, we found a profound change in the foliation pattern of the cerebellum. Strikingly, our results indicated aberrant Purkinje cells arborization at P9 and accelerated cell death at P6 and P9. We found defects in cerebellar cell proliferation and migration using a bromodeoxyuridine (BrdU)-based cell proliferation assay at postnatal day 7. Our data demonstrate that dysregulation of ADK expression during brain development profoundly affects brain growth and differentiation.
    MeSH term(s) Mice ; Animals ; Humans ; Adenosine Kinase/genetics ; Adenosine Kinase/metabolism ; Brain/metabolism ; Mice, Transgenic ; Cerebellum/metabolism ; Protein Isoforms/metabolism
    Chemical Substances Adenosine Kinase (EC 2.7.1.20) ; Protein Isoforms
    Language English
    Publishing date 2023-11-14
    Publishing country England
    Document type Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-023-47098-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Adenosine Kinase Expression Determines DNA Methylation in Cancer Cell Lines.

    Wahba, Amir E / Fedele, Denise / Gebril, Hoda / AlHarfoush, Enmar / Toti, Kiran S / Jacobson, Kenneth A / Boison, Detlev

    ACS pharmacology & translational science

    2021  Volume 4, Issue 2, Page(s) 680–686

    Abstract: DNA methylation has a major role in cancer, and its inhibitors are used therapeutically. DNA methylation depends on methyl group flux through the transmethylation pathway, which forms adenosine. We hypothesized that an adenosine kinase isoform with ... ...

    Abstract DNA methylation has a major role in cancer, and its inhibitors are used therapeutically. DNA methylation depends on methyl group flux through the transmethylation pathway, which forms adenosine. We hypothesized that an adenosine kinase isoform with nuclear expression (ADK-L) determines global DNA methylation in cancer cells. We quantified ADK-L expression (Western Blot) and global DNA methylation as percent 5-methyldeoxycytidine (5mdC, LC-MS/MS) in three cancer lines (HeLa, HepG2, and U373). ADK-L expression and global DNA methylation correlated positively with the highest levels in HeLa cells compared to U373 and HepG2 cells. To determine whether ADK increases global DNA methylation and to validate its potential therapeutics, we treated HeLa cells with potent ADK inhibitors MRS4203 and MRS4380 (IC
    Language English
    Publishing date 2021-02-16
    Publishing country United States
    Document type Journal Article
    ISSN 2575-9108
    ISSN (online) 2575-9108
    DOI 10.1021/acsptsci.1c00008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Reductive N-alkylation of nitroarenes: a green approach for the N-alkylation of natural products.

    Wahba, Amir E / Hamann, Mark T

    The Journal of organic chemistry

    2012  Volume 77, Issue 10, Page(s) 4578–4585

    Abstract: A simple, mild, cost-effective, and green approach for the reductive mono-N-alkylation of nitroarenes has been developed. HOAc/Zn are utilized as the reducing system together with a carbonyl compound as an alkyl source in methanol. Excellent yields were ... ...

    Abstract A simple, mild, cost-effective, and green approach for the reductive mono-N-alkylation of nitroarenes has been developed. HOAc/Zn are utilized as the reducing system together with a carbonyl compound as an alkyl source in methanol. Excellent yields were obtained with stoichiometric control of mono- over dialkylated products. Application to five complex natural products demonstrated the practical utility of the method.
    MeSH term(s) Alkylation ; Biological Products/chemistry ; Catalysis ; Molecular Structure ; Nitro Compounds/chemistry
    Chemical Substances Biological Products ; Nitro Compounds
    Language English
    Publishing date 2012-04-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/jo300303d
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: New one-pot methodologies for the modification or synthesis of alkaloid scaffolds.

    Wahba, Amir E / Hamann, Mark T

    Marine drugs

    2010  Volume 8, Issue 8, Page(s) 2395–2416

    Abstract: There are several avenues by which promising bioactive natural products can be produced in sufficient quantities to enable lead optimization and medicinal chemistry studies. The total synthesis of natural products is an important, but sometimes difficult, ...

    Abstract There are several avenues by which promising bioactive natural products can be produced in sufficient quantities to enable lead optimization and medicinal chemistry studies. The total synthesis of natural products is an important, but sometimes difficult, approach and requires the development of innovative synthetic methodologies to simplify the synthesis of complex molecules. Various classes of natural product alkaloids are both common and widely distributed in plants, bacteria, fungi, insects and marine organisms. This mini-review will discuss the scope, mechanistic insights and enantioselectivity aspects of selected examples of recently developed one-pot methods that have been published in 2009 for the synthesis of substituted piperidines, quinolizidines, pyrrolidines, hexahydropyrrolizines, octahydroindolizines and γ-lactams. In addition, progress on the synthesis of β-carboline (manzamine) alkaloids will also be discussed.
    MeSH term(s) Alkaloids/chemical synthesis ; Alkaloids/chemistry ; Animals ; Aquatic Organisms ; Biological Products/chemical synthesis ; Biological Products/chemistry ; Lactams/chemical synthesis ; Lactams/chemistry ; Piperidines/chemical synthesis ; Piperidines/chemistry ; Porifera ; Pyrrolidines/chemical synthesis ; Pyrrolidines/chemistry ; Stereoisomerism
    Chemical Substances Alkaloids ; Biological Products ; Lactams ; Piperidines ; Pyrrolidines
    Language English
    Publishing date 2010-08-24
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S. ; Review
    ZDB-ID 2175190-0
    ISSN 1660-3397 ; 1660-3397
    ISSN (online) 1660-3397
    ISSN 1660-3397
    DOI 10.3390/md8082395
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Ergosterol Peroxide from the Egyptian Red Lingzhi or Reishi Mushroom, Ganoderma resinaceum (Agaricomycetes), Showed Preferred Inhibition of MCF-7 over MDA-MB-231 Breast Cancer Cell Lines.

    El-Sherif, Neveen F / Ahmed, Safwat A / Ibrahim, Amany K / Habib, Eman S / El-Fallal, Amira A / El-Sayed, Ahmed K / Wahba, Amir E

    International journal of medicinal mushrooms

    2020  Volume 22, Issue 4, Page(s) 389–396

    Abstract: Ergosterol peroxide and ganoderic acid AMI were isolated for the first time from the mycelium ...

    Abstract Ergosterol peroxide and ganoderic acid AMI were isolated for the first time from the mycelium of the Egyptian Ganoderma resinaceum mushroom. The structure of these two metabolites was established by detailed analysis of 1D and 2D NMR. The isolated compounds were tested for their antitumor in vitro activities in MCF-7 and MDA-MB-231 breast cancer cell lines. Ergosterol peroxide showed preferred inhibition of MCF-7 (ER +ve) cell lines relative to MDA-MB-231 (ER -ve) cell lines with an IC50 of 1.18 μM and 12.82 μM respectively. Our data suggest that ergosterol peroxide targets estrogen receptors.
    MeSH term(s) Antineoplastic Agents/chemistry ; Antineoplastic Agents/isolation & purification ; Antineoplastic Agents/pharmacology ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Egypt ; Ergosterol/analogs & derivatives ; Ergosterol/chemistry ; Ergosterol/isolation & purification ; Ergosterol/pharmacology ; Ganoderma/chemistry ; Humans ; Inhibitory Concentration 50 ; MCF-7 Cells ; Molecular Structure ; Mycelium/chemistry ; Receptors, Estrogen/metabolism ; Triterpenes/chemistry ; Triterpenes/isolation & purification ; Triterpenes/pharmacology
    Chemical Substances Antineoplastic Agents ; Receptors, Estrogen ; Triterpenes ; ganoderic acid ; ergosterol-5,8-peroxide (UG9TN81TGH) ; Ergosterol (Z30RAY509F)
    Language English
    Publishing date 2020-06-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2108803-2
    ISSN 1940-4344 ; 1521-9437
    ISSN (online) 1940-4344
    ISSN 1521-9437
    DOI 10.1615/IntJMedMushrooms.2020034223
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Acantholactone, a new manzamine related alkaloid with an unprecedented δ-lactone and ε-lactam ring system.

    Wahba, Amir E / Fromentin, Yann / Zou, Yike / Hamann, Mark T

    Tetrahedron letters

    2012  Volume 53, Issue 47, Page(s) 6329–6331

    Abstract: A new manzamine-related alkaloid with unprecedented δ-lactone and ε-lactam rings called acantholactone ( ...

    Abstract A new manzamine-related alkaloid with unprecedented δ-lactone and ε-lactam rings called acantholactone (
    Language English
    Publishing date 2012-09-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 204287-3
    ISSN 1873-3581 ; 0040-4039
    ISSN (online) 1873-3581
    ISSN 0040-4039
    DOI 10.1016/j.tetlet.2012.08.140
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Reductive N-Alkylation of Nitroarenes: A Green Approach for the N-Alkylation of Natural Products

    Wahba, Amir E / Hamann Mark T

    Journal of organic chemistry. 2012 May 18, v. 77, no. 10

    2012  

    Abstract: A simple, mild, cost-effective, and green approach for the reductive mono-N-alkylation of nitroarenes has been developed. HOAc/Zn are utilized as the reducing system together with a carbonyl compound as an alkyl source in methanol. Excellent yields were ... ...

    Abstract A simple, mild, cost-effective, and green approach for the reductive mono-N-alkylation of nitroarenes has been developed. HOAc/Zn are utilized as the reducing system together with a carbonyl compound as an alkyl source in methanol. Excellent yields were obtained with stoichiometric control of mono- over dialkylated products. Application to five complex natural products demonstrated the practical utility of the method.
    Keywords alkylation ; cost effectiveness ; methanol ; organic chemistry ; zinc
    Language English
    Dates of publication 2012-0518
    Size p. 4578-4585.
    Publishing place American Chemical Society
    Document type Article
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021%2Fjo300303d
    Database NAL-Catalogue (AGRICOLA)

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  8. Article ; Online: Developmental Role of Adenosine Kinase in the Cerebellum.

    Gebril, Hoda / Wahba, Amir / Zhou, Xiaofeng / Lai, Tho / Alharfoush, Enmar / DiCicco-Bloom, Emanuel / Boison, Detlev

    eNeuro

    2021  Volume 8, Issue 3

    Abstract: Adenosine acts as a neuromodulator and metabolic regulator of the brain through receptor dependent and independent mechanisms. In the brain, adenosine is tightly controlled through its metabolic enzyme adenosine kinase (ADK), which exists in a ... ...

    Abstract Adenosine acts as a neuromodulator and metabolic regulator of the brain through receptor dependent and independent mechanisms. In the brain, adenosine is tightly controlled through its metabolic enzyme adenosine kinase (ADK), which exists in a cytoplasmic (ADK-S) and nuclear (ADK-L) isoform. We recently discovered that ADK-L contributes to adult hippocampal neurogenesis regulation. Although the cerebellum (CB) is a highly plastic brain area with a delayed developmental trajectory, little is known about the role of ADK. Here, we investigated the developmental profile of ADK expression in C57BL/6 mice CB and assessed its role in developmental and proliferative processes. We found high levels of ADK-L during cerebellar development, which was maintained into adulthood. This pattern contrasts with that of the cerebrum, in which ADK-L expression is gradually downregulated postnatally and largely restricted to astrocytes in adulthood. Supporting a functional role in cell proliferation, we found that the ADK inhibitor 5-iodotubericine (5-ITU) reduced DNA synthesis of granular neuron precursors in a concentration-dependent manner
    MeSH term(s) Adenosine Kinase/genetics ; Adenosine Kinase/metabolism ; Animals ; Astrocytes/metabolism ; Cerebellum/metabolism ; Mice ; Mice, Inbred C57BL ; Neurons/metabolism
    Chemical Substances Adenosine Kinase (EC 2.7.1.20)
    Language English
    Publishing date 2021-06-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2800598-3
    ISSN 2373-2822 ; 2373-2822
    ISSN (online) 2373-2822
    ISSN 2373-2822
    DOI 10.1523/ENEURO.0011-21.2021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: New cytotoxic cyclic peroxide acids from

    Hoye, Thomas R / Alarif, Walied M / Basaif, Salim S / Abo-Elkarm, Mohamed / Hamann, Mark T / Wahba, Amir E / Ayyad, Seif-Eldin N

    ARKIVOC : free online journal of organic chemistry

    2015  Volume 2015, Issue 5, Page(s) 164–175

    Abstract: Bioassay-guided fractionation of the extract of Jamaican marine ... ...

    Abstract Bioassay-guided fractionation of the extract of Jamaican marine sponge
    Language English
    Publishing date 2015-04-05
    Publishing country Switzerland
    Document type Journal Article
    ISSN 1551-7004
    ISSN 1551-7004
    DOI 10.3998/ark.5550190.p008.948
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Slow-Binding Inhibition of Mycobacterium tuberculosis Shikimate Kinase by Manzamine Alkaloids.

    Simithy, Johayra / Fuanta, Ngolui Rene / Alturki, Mansour / Hobrath, Judith V / Wahba, Amir E / Pina, Ivett / Rath, Jnanendra / Hamann, Mark T / DeRuiter, Jack / Goodwin, Douglas C / Calderón, Angela I

    Biochemistry

    2018  Volume 57, Issue 32, Page(s) 4923–4933

    Abstract: ... inhibitors: manzamine A (1), 8-hydroxymanzamine A (2), manzamine E (3), manzamine F (4), 6-deoxymanzamine X ...

    Abstract Tuberculosis represents a significant public health crisis. There is an urgent need for novel molecular scaffolds against this pathogen. We screened a small library of marine-derived compounds against shikimate kinase from Mycobacterium tuberculosis ( MtSK), a promising target for antitubercular drug development. Six manzamines previously shown to be active against M. tuberculosis were characterized as MtSK inhibitors: manzamine A (1), 8-hydroxymanzamine A (2), manzamine E (3), manzamine F (4), 6-deoxymanzamine X (5), and 6-cyclohexamidomanzamine A (6). All six showed mixed noncompetitive inhibition of MtSK. The lowest K
    MeSH term(s) Carbazoles/pharmacology ; Enzyme Activation/drug effects ; Enzyme Inhibitors/pharmacology ; Indole Alkaloids/pharmacology ; Kinetics ; Mycobacterium tuberculosis/enzymology ; Phosphotransferases (Alcohol Group Acceptor)/metabolism
    Chemical Substances Carbazoles ; Enzyme Inhibitors ; Indole Alkaloids ; manzamine E ; manzamine F ; manzamine A (104196-68-1) ; Phosphotransferases (Alcohol Group Acceptor) (EC 2.7.1.-) ; shikimate kinase (EC 2.7.1.71)
    Language English
    Publishing date 2018-07-31
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1108-3
    ISSN 1520-4995 ; 0006-2960
    ISSN (online) 1520-4995
    ISSN 0006-2960
    DOI 10.1021/acs.biochem.8b00231
    Database MEDical Literature Analysis and Retrieval System OnLINE

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