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  1. Article ; Online: An orchestrated program regulating secretory pathway genes and cargos by the transmembrane transcription factor CREB-H.

    Barbosa, Sónia / Fasanella, Giovanna / Carreira, Suzanne / Llarena, Marta / Fox, Rebecca / Barreca, Cristina / Andrew, Deborah / O'Hare, Peter

    Traffic (Copenhagen, Denmark)

    2013  Volume 14, Issue 4, Page(s) 382–398

    Abstract: CREB3 proteins comprise a set of ER-localized bZip transcription factors defined by the presence of a transmembrane domain. They are regulated by inter-compartmental transport, Golgi cleavage and nuclear transport where they promote appropriate ... ...

    Abstract CREB3 proteins comprise a set of ER-localized bZip transcription factors defined by the presence of a transmembrane domain. They are regulated by inter-compartmental transport, Golgi cleavage and nuclear transport where they promote appropriate transcriptional responses. Although CREB3 proteins play key roles in differentiation, inflammation and metabolism, a general framework relating their defining features to these diverse activities is lacking. We identify unique features of CREB3 organization including the ATB domain, which we show it is essential for transcriptional activity. This domain is absent in all other human bZip factors, but conserved in Drosophila CREBA, which controls secretory pathway genes (SPGs). Furthermore, each of the five human CREB3 factors was capable of activating SPGs in Drosophila, dependent upon the ATB domain. Expression of the CREB3 protein, CREB-H, in 293 cells, upregulated genes involved in secretory capacity, extracellular matrix formation and lipid metabolism and increased secretion of specific cargos. In liver cells, which normally express CREB-H, the active form specifically induced secretion of apolipoproteins, including ApoA-IV, ApoAI, consistent with data implicating CREB-H in metabolic homeostasis. Based on these data and other recent studies, we propose a general role for the CREB3 family in regulating secretory capacity, with particular relevance to specialized cargos.
    MeSH term(s) Apolipoproteins/metabolism ; Cell Membrane/metabolism ; Cyclic AMP Response Element-Binding Protein/chemistry ; Cyclic AMP Response Element-Binding Protein/genetics ; Cyclic AMP Response Element-Binding Protein/metabolism ; Cyclic AMP Response Element-Binding Protein A/chemistry ; Cyclic AMP Response Element-Binding Protein A/genetics ; Drosophila Proteins/chemistry ; Drosophila Proteins/genetics ; Extracellular Matrix/metabolism ; Gene Expression Regulation ; HEK293 Cells ; Hep G2 Cells ; Humans ; Lipid Metabolism ; Protein Structure, Tertiary ; Secretory Pathway/genetics ; Sequence Deletion ; Transcription, Genetic
    Chemical Substances Apolipoproteins ; CrebA protein, Drosophila ; Cyclic AMP Response Element-Binding Protein ; Cyclic AMP Response Element-Binding Protein A ; Drosophila Proteins
    Language English
    Publishing date 2013-01-24
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1483852-7
    ISSN 1600-0854 ; 1398-9219
    ISSN (online) 1600-0854
    ISSN 1398-9219
    DOI 10.1111/tra.12038
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Xenoestrogens and the induction of proliferative effects in breast cancer cells via direct activation of oestrogen receptor alpha.

    Recchia, A G / Vivacqua, A / Gabriele, S / Carpino, A / Fasanella, G / Rago, V / Bonofiglio, D / Maggiolini, M

    Food additives and contaminants

    2004  Volume 21, Issue 2, Page(s) 134–144

    Abstract: Environmental contamination with a variety of industrial products has been associated with developmental and reproductive abnormalities in wildlife species. Increasing evidence has suggested that bisphenol A (BPA) and 4-nonylphenol (NPH), two major ... ...

    Abstract Environmental contamination with a variety of industrial products has been associated with developmental and reproductive abnormalities in wildlife species. Increasing evidence has suggested that bisphenol A (BPA) and 4-nonylphenol (NPH), two major endocrine-disrupting chemicals, might be responsible for adverse effects on humans as a consequence of ubiquitous use together with potential oestrogen-like activity. To provide insight into the oestrogen-like nature of BPA and NPH, their ability to activate a reporter gene construct via an oestrogen response element in the hormone-dependent breast cancer cell lines MCF7 and T47D was ascertained. Both compounds transactivated the endogenous oestrogen receptor (ER) alpha in a direct fashion since the anti-oestrogen 4-hydroxytamoxifen abolished the response. In addition, using steroid-receptor-negative HeLa cells engineered to express ERalpha and ERbeta and the hormone-binding domains of both ERalpha and ERbeta, BPA and NPH confirmed the direct transcriptional activity. Interestingly these properties were supported in MCF7 cells by the ability to autoregulate ERalpha expression as well as to induce its nuclear compartmentalization. We therefore evaluated by reverse transcriptase polymerase chain reaction the expression of oestrogen-controlled genes such as cathepsin D and TFF1 (formerly pS2), which were increased by both chemicals tested. The agonistic effects exhibited in all assays performed prompted the evaluation of a more complex biological response such as the proliferation of MCF7 and T47D cells. The same concentration of xenoestrogens eliciting substantial transcriptional activity significantly stimulated the proliferation of both breast cancer cell lines, although with a reduced effectiveness with respect to the natural hormone 17beta-oestradiol. The results indicate that the biological action of environmental oestrogen such as BPA and NPH should be taken into account for the potential impact on human disease-like hormone-dependent breast cancer. However, further studies are needed to clarify their bioavailability and metabolism as well as whether compound mixtures could produce noticeable effects by synergistic activity.
    MeSH term(s) Benzhydryl Compounds ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Cathepsin D/biosynthesis ; Cell Division/drug effects ; Cell Line, Tumor ; Estrogen Receptor alpha ; Estrogen Receptor beta ; Estrogens/pharmacology ; Female ; Gene Expression Regulation, Neoplastic/drug effects ; Homeostasis/drug effects ; Humans ; Neoplasms, Hormone-Dependent/metabolism ; Neoplasms, Hormone-Dependent/pathology ; Peptides/metabolism ; Phenols/pharmacology ; Proteins ; Receptors, Estrogen/drug effects ; Receptors, Estrogen/genetics ; Receptors, Estrogen/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Transcriptional Activation/drug effects ; Transfection ; Trefoil Factor-1 ; Tumor Suppressor Proteins
    Chemical Substances Benzhydryl Compounds ; Estrogen Receptor alpha ; Estrogen Receptor beta ; Estrogens ; Peptides ; Phenols ; Proteins ; Receptors, Estrogen ; TFF1 protein, human ; Trefoil Factor-1 ; Tumor Suppressor Proteins ; Cathepsin D (EC 3.4.23.5) ; 4-nonylphenol (I03GBV4WEL) ; bisphenol A (MLT3645I99)
    Language English
    Publishing date 2004-02
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 49417-3
    ISSN 0265-203X
    ISSN 0265-203X
    DOI 10.1080/02652030310001641177
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Xenoestrogens and the induction of proliferative effects in breast cancer cells via direct activation of oestrogen receptor α

    Recchia, A.G / Vivacqua, A / Gabriele, S / Carpino, A / Fasanella, G / Rago, V / Bonofiglio, D / Maggiolini, M

    Food additives and contaminants. 2004 Feb., v. 21, no. 2

    2004  

    Keywords xenoestrogens ; endocrine-disrupting chemicals ; hormone antagonists ; estradiol ; breast neoplasms ; cell lines ; cell culture ; steroidogenesis ; hormone receptors ; transcriptional activation ; reporter genes ; cell proliferation ; messenger RNA ; cathepsins ; gene overexpression ; luciferase ; signal transduction ; estrogenic properties ; health effects assessments
    Language English
    Dates of publication 2004-02
    Size p. 134-144.
    Document type Article
    ZDB-ID 49417-3
    ISSN 1464-5122 ; 0265-203X
    ISSN (online) 1464-5122
    ISSN 0265-203X
    Database NAL-Catalogue (AGRICOLA)

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  4. Article: Differential phosphorylation of c-Jun and JunD in response to the epidermal growth factor is determined by the structure of MAPK targeting sequences.

    Vinciguerra, Maria / Vivacqua, Adele / Fasanella, Giovanna / Gallo, Adriana / Cuozzo, Concetta / Morano, Annalisa / Maggiolini, Marcello / Musti, Anna Maria

    The Journal of biological chemistry

    2003  Volume 279, Issue 10, Page(s) 9634–9641

    Abstract: MAPK phosphorylation of various substrates is mediated by the presence of docking sites, including the D domain and the DEF motif. Depending on the number and sequences of these domains, substrates are phosphorylated by specific subsets of MAPKs. For ... ...

    Abstract MAPK phosphorylation of various substrates is mediated by the presence of docking sites, including the D domain and the DEF motif. Depending on the number and sequences of these domains, substrates are phosphorylated by specific subsets of MAPKs. For example, a D domain targets JNK to c-Jun, whereas a DEF motif is required for ERK phosphorylation of c-Fos. JunD, in contrast, contains both D and DEF domains. Here we show that these motifs mediate JunD phosphorylation in response to either ERK or JNK activation. An intact D domain is required for phosphorylation and activation of JunD by both subtypes of MAPK. The DEF motif acts together with the D domain to elicit efficient phosphorylation of JunD in response to the epidermal growth factor (EGF) but has no function on JunD phosphorylation and activation by JNK signaling. Furthermore, we show that conversion of a c-Jun sequence to a canonical DEF domain, as it is present in JunD, elicits c-Jun activation in response to EGF. Our results suggest that evolution of a particular modular system of MAPK targeting sequences has determined a differential response of JunD and c-Jun to ERK activation.
    MeSH term(s) Amino Acid Sequence ; Animals ; Binding Sites/genetics ; Cell Line ; Epidermal Growth Factor/metabolism ; Humans ; JNK Mitogen-Activated Protein Kinases ; Mice ; Mitogen-Activated Protein Kinases/genetics ; Mitogen-Activated Protein Kinases/metabolism ; Molecular Sequence Data ; Phosphorylation ; Protein Structure, Tertiary ; Sequence Analysis ; Signal Transduction ; Structure-Activity Relationship
    Chemical Substances Epidermal Growth Factor (62229-50-9) ; JNK Mitogen-Activated Protein Kinases (EC 2.7.11.24) ; Mitogen-Activated Protein Kinases (EC 2.7.11.24)
    Language English
    Publishing date 2003-12-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1074/jbc.M308721200
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: The mutant androgen receptor T877A mediates the proliferative but not the cytotoxic dose-dependent effects of genistein and quercetin on human LNCaP prostate cancer cells.

    Maggiolini, Marcello / Vivacqua, Adele / Carpino, Amalia / Bonofiglio, Daniela / Fasanella, Giovanna / Salerno, Michele / Picard, Didier / Andó, Sebastiano

    Molecular pharmacology

    2002  Volume 62, Issue 5, Page(s) 1027–1035

    Abstract: High consumption of soybean products, such as phytoestrogens, has been hypothesized to contribute to a reduced incidence of prostate cancer in Southeast Asian people, although there have been inconsistent results among studies. Human LNCaP cells, ... ...

    Abstract High consumption of soybean products, such as phytoestrogens, has been hypothesized to contribute to a reduced incidence of prostate cancer in Southeast Asian people, although there have been inconsistent results among studies. Human LNCaP cells, extensively used as a model for androgen-dependent prostate tumor, express the androgen receptor (AR) mutant T877A promiscuously transactivated by estrogens and other ligands, which may further facilitate cancer progression. Here, for the first time to our knowledge, we demonstrate that genistein and quercetin, two phytoestrogens abundantly present in soybeans, activate either the AR mutant T877A in LNCaP or in transfected Chinese hamster ovary cells. This observation is supported by their capability to induce AR accumulation in the nuclear compartment of LNCaP together with mRNA down-regulation of the androgen target genes AR and PAP, and PSA up-regulation. Of interest, at concentrations eliciting transcriptional activity, both genistein and quercetin stimulate LNCaP cell growth, whereas at high levels, they become cytotoxic independently of AR expression, as ascertained in steroid receptor-negative Hela cells. The results of our study provide evidence that phytoestrogens may regulate several signaling processes in LNCaP cells; however, further studies are needed to assess their potential capability to restrain prostate tumor progression.
    MeSH term(s) Active Transport, Cell Nucleus/drug effects ; Animals ; CHO Cells ; Cell Division/drug effects ; Cricetinae ; Dose-Response Relationship, Drug ; Gene Expression/drug effects ; Genistein/pharmacology ; HeLa Cells ; Humans ; Male ; Prostate-Specific Antigen/genetics ; Prostatic Neoplasms/pathology ; Quercetin/pharmacology ; RNA, Messenger ; Receptors, Androgen/genetics ; Receptors, Androgen/physiology ; Tumor Cells, Cultured ; Up-Regulation/drug effects
    Chemical Substances RNA, Messenger ; Receptors, Androgen ; Quercetin (9IKM0I5T1E) ; Genistein (DH2M523P0H) ; Prostate-Specific Antigen (EC 3.4.21.77)
    Language English
    Publishing date 2002-09-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 124034-1
    ISSN 1521-0111 ; 0026-895X
    ISSN (online) 1521-0111
    ISSN 0026-895X
    DOI 10.1124/mol.62.5.1027
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: The G protein-coupled receptor GPR30 mediates c-fos up-regulation by 17beta-estradiol and phytoestrogens in breast cancer cells.

    Maggiolini, Marcello / Vivacqua, Adele / Fasanella, Giovanna / Recchia, Anna Grazia / Sisci, Diego / Pezzi, Vincenzo / Montanaro, Daniela / Musti, Anna Maria / Picard, Didier / Andò, Sebastiano

    The Journal of biological chemistry

    2004  Volume 279, Issue 26, Page(s) 27008–27016

    Abstract: A growing body of evidence concerning estrogen effects cannot be explained by the classic model of hormone action, which involves the binding to estrogen receptors (ERs) alpha and ERbeta and the interaction of the steroid-receptor complex with specific ... ...

    Abstract A growing body of evidence concerning estrogen effects cannot be explained by the classic model of hormone action, which involves the binding to estrogen receptors (ERs) alpha and ERbeta and the interaction of the steroid-receptor complex with specific DNA sequences associated with target genes. Using c-fos proto-oncogene expression as an early molecular sensor of estrogen action in ERalpha-positive MCF7 and ER-negative SKBR3 breast cancer cells, we have discovered that 17beta-estradiol (E2), and the two major phytoestrogens, genistein and quercetin, stimulate c-fos expression through ERalpha as well as through an ER-independent manner via the G protein-coupled receptor homologue GPR30. The c-fos response is repressed in GPR30-expressing SKBR3 cells transfected with an antisense oligonucleotide against GPR30 and reconstituted in GPR30-deficient MDA-MB 231 and BT-20 breast cancer cells transfected with a GPR30 expression vector. GPR30-dependent activation of ERK1/2 by E2 and phytoestrogens occurs via a Gbetagamma-associated pertussis toxin-sensitive pathway that requires both Src-related and EGF receptor tyrosine kinase activities. The ability of E2 and phytoestrogens to regulate the expression of growth-related genes such as c-fos even in the absence of ER has interesting implications for understanding breast cancer progression.
    MeSH term(s) Breast Neoplasms/genetics ; Breast Neoplasms/metabolism ; Cell Line, Tumor ; Estradiol/pharmacology ; Estrogen Receptor alpha ; Genistein/pharmacology ; Humans ; Isoflavones/pharmacology ; Mitogen-Activated Protein Kinase 1/metabolism ; Mitogen-Activated Protein Kinase 3 ; Mitogen-Activated Protein Kinases/metabolism ; Oligoribonucleotides, Antisense/pharmacology ; Phosphorylation ; Phytoestrogens ; Plant Preparations/pharmacology ; Plasmids/genetics ; Proto-Oncogene Proteins c-fos/antagonists & inhibitors ; Proto-Oncogene Proteins c-fos/biosynthesis ; Proto-Oncogene Proteins c-fos/genetics ; Quercetin/pharmacology ; RNA, Messenger/biosynthesis ; Receptors, Estrogen/metabolism ; Receptors, G-Protein-Coupled/genetics ; Receptors, G-Protein-Coupled/physiology ; Signal Transduction ; Transcriptional Activation/drug effects ; Transfection ; Up-Regulation/drug effects
    Chemical Substances Estrogen Receptor alpha ; GPER1 protein, human ; Isoflavones ; Oligoribonucleotides, Antisense ; Phytoestrogens ; Plant Preparations ; Proto-Oncogene Proteins c-fos ; RNA, Messenger ; Receptors, Estrogen ; Receptors, G-Protein-Coupled ; Estradiol (4TI98Z838E) ; Quercetin (9IKM0I5T1E) ; Genistein (DH2M523P0H) ; Mitogen-Activated Protein Kinase 1 (EC 2.7.11.24) ; Mitogen-Activated Protein Kinase 3 (EC 2.7.11.24) ; Mitogen-Activated Protein Kinases (EC 2.7.11.24)
    Language English
    Publishing date 2004-04-16
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1074/jbc.M403588200
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The food contaminants bisphenol A and 4-nonylphenol act as agonists for estrogen receptor alpha in MCF7 breast cancer cells.

    Vivacqua, Adele / Recchia, Anna Grazia / Fasanella, Giovanna / Gabriele, Sabrina / Carpino, Amalia / Rago, Vittoria / Di Gioia, Maria Luisa / Leggio, Antonella / Bonofiglio, Daniela / Liguori, Angelo / Maggiolini, Marcello

    Endocrine

    2003  Volume 22, Issue 3, Page(s) 275–284

    Abstract: Xenoestrogens are chemically distinct industrial products potentially able to disrupt the endocrine system by mimicking the action of endogenous steroid hormones. Among such compounds, the ubiquitous environmental contaminants bisphenol A (BPA) and 4- ... ...

    Abstract Xenoestrogens are chemically distinct industrial products potentially able to disrupt the endocrine system by mimicking the action of endogenous steroid hormones. Among such compounds, the ubiquitous environmental contaminants bisphenol A (BPA) and 4-nonylphenol (NPH) may promote adverse effects in humans triggering estrogenic signals in target tissues. Following a research program on human exposure to endocrine disruptors, we found contamination of fresh food by BPA and NPH. More important, these contaminants were found to display estrogen-like activity using as a model system the estrogen-dependent MCF7 breast cancer cells (MCF7wt); its variant named MCF7SH, which is hormone-independent but still ERalpha-positive, and the steroid receptor-negative human cervical carcinoma HeLa cells. In transfection experiments BPA and NPH activated in a direct manner the endogenous ERalpha in MCF7wt and MCF7SH cells, as the antiestrogen hydroxytamoxifen was able to reverse both responses. Moreover, only the hormone-binding domains of ERalpha and ERbeta expressed by chimeric proteins in HeLa cells were sufficient to elicit the transcriptional activity upon BPA and NPH treatments. Transfecting the same cell line with ERalpha mutants, both contaminants triggered an estrogen-like response. These transactivation properties were interestingly supported in MCF7wt cells by the autoregulation of ERalpha which was assessed by RT-PCR for the mRNA evaluation and by immunoblotting and immunocytochemistry for the determination of protein levels. The ability of BPA and NPH to modulate gene expression was further confirmed by the upregulation of an estrogen target gene like pS2. As a biological counterpart, concentrations of xenoestrogens eliciting transcriptional activity were able to stimulate the proliferation of MCF7wt and MCFSH cells. Only NPH at a dose likely too high to be of any physiological relevance induced a severe cytotoxicity in an ERalpha-independent manner as ascertained in HeLa cells. The estrogenic effects of such industrial agents together with an increasing widespread human exposure should be taken into account for the potential influence also on hormone-dependent breast cancer disease.
    MeSH term(s) Benzhydryl Compounds ; Blotting, Western ; Breast Neoplasms/genetics ; Breast Neoplasms/metabolism ; Cell Division/drug effects ; Cell Line, Tumor ; Environmental Pollutants/pharmacology ; Estrogen Receptor alpha ; Estrogens, Non-Steroidal/pharmacology ; Female ; Food Contamination ; Gene Expression Regulation, Neoplastic/drug effects ; Humans ; Immunohistochemistry ; Neoplasms, Hormone-Dependent/genetics ; Neoplasms, Hormone-Dependent/metabolism ; Phenols/pharmacology ; RNA, Messenger/biosynthesis ; RNA, Messenger/genetics ; Receptors, Estrogen/agonists ; Receptors, Estrogen/biosynthesis ; Receptors, Estrogen/genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Transcriptional Activation/drug effects ; Transfection
    Chemical Substances Benzhydryl Compounds ; Environmental Pollutants ; Estrogen Receptor alpha ; Estrogens, Non-Steroidal ; Phenols ; RNA, Messenger ; Receptors, Estrogen ; 4-nonylphenol (I03GBV4WEL) ; bisphenol A (MLT3645I99)
    Language English
    Publishing date 2003-12
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1194484-5
    ISSN 1355-008X ; 0969-711X
    ISSN 1355-008X ; 0969-711X
    DOI 10.1385/ENDO:22:3:275
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Oestrogen receptor beta is required for androgen-stimulated proliferation of LNCaP prostate cancer cells.

    Maggiolini, Marcello / Recchia, Anna Grazia / Carpino, Amalia / Vivacqua, Adele / Fasanella, Giovanna / Rago, Vittoria / Pezzi, Vincenzo / Briand, Pierre-André / Picard, Didier / Andò, Sebastiano

    Journal of molecular endocrinology

    1996  Volume 32, Issue 3, Page(s) 777–791

    Abstract: The role of oestrogens in the development of prostate cancer is poorly understood. However, a large body of evidence has suggested that oestrogenic hormones may be involved in prostatic malignancy. The localization of oestrogen receptor beta (ERbeta) in ... ...

    Abstract The role of oestrogens in the development of prostate cancer is poorly understood. However, a large body of evidence has suggested that oestrogenic hormones may be involved in prostatic malignancy. The localization of oestrogen receptor beta (ERbeta) in the secretory epithelium of the human prostate has raised the intriguing possibility that the action of oestrogen could be mediated, at least in part, by this receptor during the process of carcinogenesis. Hence, specific interference with oestrogen-activated and ERbeta-mediated transcriptional activity could open new issues in the endocrine manipulation of prostate tumours. In the present study, we provide new insights into the role of ERbeta in the context of an androgen-responsive prostate cancer cell line such as LNCaP, which was used as a model system together with steroid receptor negative HeLa cells. ERbeta and the mutated androgen receptor (AR) T877A did not discriminate between oestrogen- or androgen-induced transactivation, whereas ERbeta and AR transcriptional activity were inhibited only by the respective hormone antagonists ICI 182,780 and casodex. Furthermore, the nuclear localization of ERbeta evaluated by immunocytochemistry confirmed the promiscuous response to hormones in addition to the specific inhibitory action of antagonists. Interestingly, ICI 182,780 and an ERbeta antisense expression vector repressed the growth effects of both 17beta-oestradiol and 5alpha-dihydrotestosterone, suggesting that ERbeta has a key role in the proliferation induced by these steroids in LNCaP prostate cancer cells. Thus our findings implicate ERbeta as a potential target for the treatment of prostate tumours.
    MeSH term(s) Androgen Antagonists/metabolism ; Androgens/metabolism ; Anilides/metabolism ; Cell Line, Tumor ; Cell Proliferation ; Dihydrotestosterone/metabolism ; Estradiol/analogs & derivatives ; Estradiol/metabolism ; Estrogen Antagonists/metabolism ; Estrogen Receptor beta/genetics ; Estrogen Receptor beta/metabolism ; Fulvestrant ; Genes, Reporter ; Humans ; Male ; Nitriles ; Oligonucleotides, Antisense/metabolism ; Prostatic Neoplasms/metabolism ; Receptors, Androgen/genetics ; Receptors, Androgen/metabolism ; Response Elements ; Tosyl Compounds
    Chemical Substances Androgen Antagonists ; Androgens ; Anilides ; Estrogen Antagonists ; Estrogen Receptor beta ; Nitriles ; Oligonucleotides, Antisense ; Receptors, Androgen ; Tosyl Compounds ; Dihydrotestosterone (08J2K08A3Y) ; Fulvestrant (22X328QOC4) ; Estradiol (4TI98Z838E) ; bicalutamide (A0Z3NAU9DP)
    Language English
    Publishing date 1996-07-15
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 645012-x
    ISSN 1479-6813 ; 0952-5041
    ISSN (online) 1479-6813
    ISSN 0952-5041
    DOI 10.1677/jme.0.0320777
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Measurement of single-diffractive dijet production in proton-proton collisions at

    Sirunyan, A M / Tumasyan, A / Adam, W / Ambrogi, F / Asilar, E / Bergauer, T / Brandstetter, J / Dragicevic, M / Erö, J / Valle, A Escalante Del / Flechl, M / Frühwirth, R / Ghete, V M / Hrubec, J / Jeitler, M / Krammer, N / Krätschmer, I / Liko, D / Madlener, T /
    Mikulec, I / Rad, N / Rohringer, H / Schieck, J / Schöfbeck, R / Spanring, M / Spitzbart, D / Waltenberger, W / Wittmann, J / Wulz, C-E / Zarucki, M / Chekhovsky, V / Mossolov, V / Gonzalez, J Suarez / De Wolf, E A / Croce, D Di / Janssen, X / Lauwers, J / Lelek, A / Pieters, M / Haevermaet, H Van / Mechelen, P Van / Remortel, N Van / Zeid, S Abu / Blekman, F / D'Hondt, J / De Clercq, J / Deroover, K / Flouris, G / Lontkovskyi, D / Lowette, S / Marchesini, I / Moortgat, S / Moreels, L / Python, Q / Skovpen, K / Tavernier, S / Doninck, W Van / Mulders, P Van / Parijs, I Van / Beghin, D / Bilin, B / Brun, H / Clerbaux, B / De Lentdecker, G / Delannoy, H / Dorney, B / Fasanella, G / Favart, L / Grebenyuk, A / Kalsi, A K / Lenzi, T / Luetic, J / Postiau, N / Starling, E / Thomas, L / Velde, C Vander / Vanlaer, P / Vannerom, D / Wang, Q / Cornelis, T / Dobur, D / Fagot, A / Gul, M / Khvastunov, I / Poyraz, D / Roskas, C / Trocino, D / Tytgat, M / Verbeke, W / Vermassen, B / Vit, M / 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    The European physical journal. C, Particles and fields

    2020  Volume 80, Issue 12, Page(s) 1164

    Abstract: Measurements are presented of the single-diffractive dijet cross section and the diffractive cross section as a function of the proton fractional momentum ... ...

    Abstract Measurements are presented of the single-diffractive dijet cross section and the diffractive cross section as a function of the proton fractional momentum loss
    Language English
    Publishing date 2020-12-17
    Publishing country France
    Document type Journal Article
    ZDB-ID 1459069-4
    ISSN 1434-6052 ; 1434-6044
    ISSN (online) 1434-6052
    ISSN 1434-6044
    DOI 10.1140/epjc/s10052-020-08562-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Studies of Charm Quark Diffusion inside Jets Using Pb-Pb and pp Collisions at sqrt[s_{NN}]=5.02  TeV.

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    Physical review letters

    2020  Volume 125, Issue 10, Page(s) 102001

    Abstract: The first study of charm quark diffusion with respect to the jet axis in heavy ion collisions is presented. The measurement is performed using jets with p_{T}^{jet}>60  GeV/c and D^{0} mesons with p_{T}^{D}>4  GeV/c in lead-lead (Pb-Pb) and proton-proton ...

    Abstract The first study of charm quark diffusion with respect to the jet axis in heavy ion collisions is presented. The measurement is performed using jets with p_{T}^{jet}>60  GeV/c and D^{0} mesons with p_{T}^{D}>4  GeV/c in lead-lead (Pb-Pb) and proton-proton (pp) collisions at a nucleon-nucleon center-of-mass energy of sqrt[s_{NN}]=5.02  TeV, recorded by the CMS detector at the LHC. The radial distribution of D^{0} mesons with respect to the jet axis is sensitive to the production mechanisms of the meson, as well as to the energy loss and diffusion processes undergone by its parent parton inside the strongly interacting medium produced in Pb-Pb collisions. When compared to Monte Carlo event generators, the radial distribution in pp collisions is found to be well described by pythia, while the slope of the distribution predicted by sherpa is steeper than that of the data. In Pb-Pb collisions, compared to the pp results, the D^{0} meson distribution for 4<p_{T}^{D}<20  GeV/c hints at a larger distance on average with respect to the jet axis, reflecting a diffusion of charm quarks in the medium created in heavy ion collisions. At higher p_{T}^{D}, the Pb-Pb and pp radial distributions are found to be similar.<br />
    Language English
    Publishing date 2020-09-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.125.102001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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