178,631 research outputs found

    Senescence and pre-malignancy: How do tumors progress?

    No full text
    Cellular senescence is a tumor suppressor response that has been observed both in vitro and in vivo, and features of senescence have been documented in various human premalignant lesions, including melanoma, colon and lung adenoma, prostatic intraepithelial neoplasia, and others. The fact that a subset of these lesions eventually progress to malignant invasive tumors suggests that premalignant cells can either bypass or escape the senescent response. Much work has been done to understand the mechanisms underlying such progression, but it remains unclear whether tumors progress by evasion of senescence induction, or by disruption of senescence maintenance, or whether both mechanisms can occur in human cancer development. This review presents the current evidence for mechanisms of senescence evasion and reversion, and discusses what has been learnt about this process using in vitro and in vivo experimental systems. As we learn more about the key signaling effectors of senescence, the hope is that appropriate targets will be identified for preservation and-or re-induction of senescence in human tumors. Such knowledge may also find application in better estimation of risks of cancer progression in individual premalignant lesions, which will lead to more accurate allocation of appropriate treatment options for such patients. © 2011 Elsevier Ltd.Acosta JC, 2008, CELL, V133, P1006, DOI 10.1016-j.cell.2008.03.038; Bartkova J, 2006, NATURE, V444, P633, DOI 10.1038-nature05268; Beausejour CM, 2003, EMBO J, V22, P4212, DOI 10.1093-emboj-cdg417; Berman HK, 2010, CANCER PREV RES, V3, P579, DOI 10.1158-1940-6207.CAPR-10-0073; Bihani T, 2004, CELL CYCLE, V3, P1201; Braig M, 2005, NATURE, V436, P660, DOI 10.1038-nature03841; BRASH DE, 1991, P NATL ACAD SCI USA, V88, P10124, DOI 10.1073-pnas.88.22.10124; BURCH HB, 1995, ENDOCRIN METAB CLIN, V24, P663; Busuttil RA, 2006, DNA REPAIR, V5, P52, DOI 10.1016-j.dnarep.2005.07.006; BUTTRAM VC, 1981, FERTIL STERIL, V36, P433; Campisi J, 2007, NAT REV MOL CELL BIO, V8, P729, DOI 10.1038-nrm2233; Campisi J, 2005, CELL, V120, P513, DOI 10.1016-j.cell.2005.02.003; Cappell M S, 2007, Minerva Gastroenterol Dietol, V53, P351; Chakrabarti J, 2004, BRIT J CANCER, V91, P954, DOI 10.1038-sj.bjc.6602059; Chang BD, 1999, CANCER RES, V59, P3761; Chen ZB, 2005, NATURE, V436, P725, DOI 10.1038-nature03918; Collado M, 2005, NATURE, V436, P642, DOI 10.1038-436642a; Collins LC, 2005, CANCER-AM CANCER SOC, V103, P1778, DOI 10.1002-cncr.20979; Coppe JP, 2008, PLOS BIOL, V6, P2853, DOI 10.1371-journal.pbio.0060301; Courtois-Cox S, 2006, CANCER CELL, V10, P459, DOI 10.1016-j.ccr.2006.10.003; Cristofalo VJ, 2005, EXP GERONTOL, V40, P836, DOI 10.1016-j.exger.2005.08.005; Dankort D, 2007, GENE DEV, V21, P379, DOI 10.1101-gad.1516407; Denchi EL, 2005, MOL CELL BIOL, V25, P2660, DOI 10.1128-MCB.25.7.2660-2672.2005; Dhomen N, 2009, CANCER CELL, V15, P294, DOI 10.1016-j.ccr.2009.02.022; Dickinson SI, 2010, CANCER CONTROL, V17, P214; di Fagagna FD, 2008, NAT REV CANCER, V8, P512, DOI 10.1038-nrc2440; Di Micco R, 2006, NATURE, V444, P638, DOI 10.1038-nature05327; Di Micco R, 2011, NAT CELL BIOL, V13, P292, DOI 10.1038-ncb2170; DIMRI GP, 1995, P NATL ACAD SCI USA, V92, P9363, DOI 10.1073-pnas.92.20.9363; Dirac AMG, 2003, J BIOL CHEM, V278, P11731, DOI 10.1074-jbc.C300023200; Farrell WE, 1998, ANN MED, V30, P192, DOI 10.3109-07853899808999403; Feldser DM, 2007, CANCER CELL, V11, P461, DOI 10.1016-j.ccr.2007.02.026; Ferbeyre G, 2000, GENE DEV, V14, P2015; Fonseca R, 1997, ANN INTERN MED, V127, P1013; Gauthier ML, 2007, CANCER CELL, V12, P479, DOI 10.1016-j.ccr.2007.10.017; Gire V, 1998, MOL CELL BIOL, V18, P1611; Goldman R, 2003, J NUTR, V133, p965S; Gosselin K, 2009, CANCER RES, V69, P7917, DOI 10.1158-0008-5472.CAN-08-2510; Gray-Schopfer VC, 2006, BRIT J CANCER, V95, P496, DOI 10.1038-sj.bjc.6603283; Ha L, 2007, P NATL ACAD SCI USA, V104, P10968, DOI 10.1073-pnas.0611638104; Haggman MJ, 1997, J UROLOGY, V158, P12, DOI 10.1097-00005392-199707000-00004; Hanahan D, 2000, CELL, V100, P57, DOI 10.1016-S0092-8674(00)81683-9; Hartmann LC, 2005, NEW ENGL J MED, V353, P229, DOI 10.1056-NEJMoa044383; Jasperson KW, 2010, GASTROENTEROLOGY, V138, P2044, DOI 10.1053-j.gastro.2010.01.054; Kennedy AL, 2010, CELL DIV, V5, DOI 10.1186-1747-1028-5-16; Kortlever RM, 2006, NAT CELL BIOL, V8, P877, DOI 10.1038-ncb1448; Kosar M, 2011, CELL CYCLE, V10, P457, DOI 10.4161-cc.10.3.14707; Krtolica A, 2001, P NATL ACAD SCI USA, V98, P12072, DOI 10.1073-pnas.211053698; Kuilman T, 2010, GENE DEV, V24, P2463, DOI 10.1101-gad.1971610; Kuilman T, 2008, CELL, V133, P1019, DOI 10.1016-j.cell.2008.03.039; Lee Erica H, 2010, Plast Reconstr Surg, V125, p188e, DOI 10.1097-PRS.0b013e3181d6e89a; Levy A, 2003, FRONT NEUROENDOCRIN, V24, P94, DOI 10.1016-S0091-3022(03)00012-8; Lukasova E, 2005, J LEUKOCYTE BIOL, V77, P100, DOI 10.1189-jlb.0704388; Majumder PK, 2008, CANCER CELL, V14, P146, DOI 10.1016-j.ccr.2008.06.002; Mallette FA, 2007, J BIOL CHEM, V282, P34938, DOI 10.1074-jbc.M707074200; Mallette FA, 2007, CELL CYCLE, V6, P1831; Michaloglou C, 2005, NATURE, V436, P720, DOI 10.1038-nature03890; Moiseeva O, 2006, MOL BIOL CELL, V17, P1583, DOI 10.1091-mbc.E05-09-0858; Mooi WJ, 2006, NEW ENGL J MED, V355, P1037, DOI 10.1056-NEJMra062285; Nardella C, 2008, GENE DEV, V22, P2172, DOI 10.1101-gad.1699608; Narita M, 2003, CELL, V113, P703, DOI 10.1016-S0092-8674(03)00401-X; Narita M, 2006, CELL, V126, P503, DOI 10.1016-j.cell.2006.05.052; PAGE DL, 1994, WORLD J SURG, V18, P32; Park YS, 2008, ANN SURG ONCOL, V15, P1968, DOI 10.1245-s10434-008-9927-9; Roberson RS, 2005, CANCER RES, V65, P2795, DOI 10.1158-0008-5472.CAN-04-1270; Rodier F, 2009, NAT CELL BIOL, V11, P973, DOI 10.1038-ncb1909; Saab R, 2010, THESCIENTIFICWORLDJO, V10, P727, DOI 10.1100-tsw.2010.68; Saab R, 2009, CANCER RES, V69, P440, DOI 10.1158-0008-5472.CAN-08-1892; Sabah M, 2007, APPL IMMUNOHISTO M M, V15, P64, DOI 10.1097-01.pai.0000201809.43554.ed; Sage J, 2003, NATURE, V424, P223, DOI 10.1038-nature01764; Sarkisian CJ, 2007, NAT CELL BIOL, V9, P493, DOI 10.1038-ncb1567; Schmitt CA, 2007, BBA-REV CANCER, V1775, P5, DOI 10.1016-j.bbcan.2006.08.005; Schmitt CA, 2002, CELL, V109, P335, DOI 10.1016-S0092-8674(02)00734-1; Serrano M, 2001, CURR OPIN CELL BIOL, V13, P748, DOI 10.1016-S0955-0674(00)00278-7; Shamma A, 2009, CANCER CELL, V15, P255, DOI 10.1016-j.ccr.2009.03.001; Shay JW, 2004, ONCOGENE, V23, P2919, DOI 10.1038-sj.onc.1207518; Skomedal H, 1999, GYNECOL ONCOL, V73, P223, DOI 10.1006-gyno.1999.5346; Soucek L, 2008, NATURE, V455, P679, DOI 10.1038-nature07260; STEIN GH, 1985, J CELL PHYSIOL, V122, P343, DOI 10.1002-jcp.1041220303; Sun PQ, 2007, CELL, V128, P295, DOI 10.1016-j.cell.2006.11.050; Takahashi A, 2006, NAT CELL BIOL, V8, P1291, DOI 10.1038-ncb1491; Tateishi U, 2003, RADIOGRAPHICS, V23, P1477, DOI 10.1148-rg.236015526; te Poele RH, 2002, CANCER RES, V62, P1876; Untergasser G, 2003, EXP GERONTOL, V38, P1179, DOI 10.1016-j.exger.2003.08.008; Ventura A, 2007, NATURE, V445, P661, DOI 10.1038-nature05541; Vijg J, 2005, ANN NY ACAD SCI, V1055, P35, DOI 10.1196-annals.1323.007; Wajapeyee N, 2008, CELL, V132, P363, DOI 10.1016-j.cell.2007.12.032; Wu CH, 2007, P NATL ACAD SCI USA, V104, P13028, DOI 10.1073-pnas.0701953104; Xu M, 2008, MOL CELL BIOL, V28, P1713, DOI 10.1128-MCB.01360-07; Xue W, 2007, NATURE, V445, P656, DOI 10.1038-nature05529; Young AP, 2008, NAT CELL BIOL, V10, P361, DOI 10.1038-ncb1699; Zhang RG, 2005, DEV CELL, V8, P19, DOI 10.1016-j.devcel.2004.10.019; Zhang ZH, 2006, MODERN PATHOL, V19, P1339, DOI 10.1038-modpathol.3800655; Zheng Y, 2009, OMICS, V13, P301, DOI 10.1089-omi.2009.001410111

    Communicating with terminal patients: Lessons from wit and students

    No full text
    [No abstract available]Deloney LA, 2003, TEACH LEARN MED, V15, P247, DOI 10.1207-S15328015TLM1504_06; Ellershaw J, 2003, BRIT MED J, V326, P30, DOI 10.1136-bmj.326.7379.30; Garg A, 1997, CAN MED ASSOC J, V156, P1159; Kirk P, 2004, BRIT MED J, V328, P1343, DOI 10.1136-bmj.38103.423576.55; Lloyd-Williams M, 2003, BRIT MED J, V327, P221, DOI 10.1136-bmj.327.7408.221-b; Saab BR, 2005, FAM MED, V37, P9032

    Cellular Senescence: Many Roads, One Final Destination

    No full text
    Cellular senescence is a tumor-suppressor mechanism that has been shown to occur in response to multiple signals, including oncogenic stress, DNA damage, oxidative stress, telomere shortening, and other tumor-promoting insults. Over the past decade, much has been uncovered regarding the phenotype of this tumor-suppressor response and the underlying pathways necessary for its establishment. However, we have also learned that the intricate details of signaling pathways underlying senescence as a tumor-suppressor response are very much context dependent. In addition, cross-talk among pathways, and negative and positive feedback loops, all complicate our understanding of this process. This short review attempts to summarize what is known to date regarding senescence in tumor suppression, both in vitro and in vivo. Further insights into pathways necessary for senescence will hopefully identify appropriate targets for interventions to not only induce senescence as a treatment of cancerous lesions, but also to maintain this state in premalignant lesions in an effort to prevent progression to cancer

    Resultados perinatais de transfusões intra-uterinas realizadas por doença hemolítica perinatal na maternidade Carmela Dutra - Florianópolis

    No full text
    Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina. Departamento de Tocoginecologia

    Resgate histórico do Departamento de Tocoginecologia da Universidade Federal de Santa Catarina.

    No full text
    Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina. Departamento de Tocoginecologia

    Appropriate Similarity Measures for Author Cocitation Analysis

    No full text
    We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis

    "Closing the R&D Gap, Evaluating the Sources of R&D Spending"

    No full text
    Both spending and tax policies have been implemented in the United States with the goal of stimulating private sector research and development (R&D). Karier questions whether current R&D policy, especially the research and experimentation tax credit, can contribute to closing the gap between nondefense expenditures on R&D in the United States and such expenditures in other countries, such as Japan and Germany. He also explores possible changes to our current R&D policy to make it more effective.

    Going Beyond Counting First Authors in Author Co-citation Analysis

    No full text
    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed

    Bezpečnost a ochrana zdraví při práci ve výrobní firmě Saab Czech, s.r.o.

    No full text
    The diploma thesis deals with the issue of safety and health at work in the production company Saab Czech, s. r. o. The theoretical part of the thesis approaches the issue of safety and health at work, its history, legislation, interconnection with other fields and definitions of terms that are very closely related to it. The practical part of the thesis describes the current settings of safety and health at work in company Saab Czech, s. r. o. and finds the risks that may arise. Subsequently with the help of risk matrix identify the risks that needs to be solved as a matter of priority and try to find appropriate precautions
    corecore