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Cláudia Bessa (CB) obtained her degree in Biology in 2009, and completed the master in Molecular Genetics in 2012. Hereafter, she worked as research fellow within a project granted by FCT that envisaged functional, molecular and pharmacological studies of p53 proteins in cancer. In 2013, she got a PhD scholarship from FCT under the PhD program in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto. During her PhD, CB worked on the search for new pharmacological modulators of PKC isozymes with potential application on cancer therapy using a chemical library of natural and semi-synthetic compounds. Remarkably, she identified the first small-molecule PKCdelta-selective activator, showing its promising antitumor activity in colorectal cancer (CRC). This study was carried out in collaboration with M. Kazanietz (University of Pennsylvania, USA), which allowed her to acquire a deepen expertise in PKC pharmacology and PKC-regulated signaling pathways in cancer. Furthermore, she got training at other national institutions, including Faculty of Medicine-UP and CNC-Center for Neuroscience and Cell Biology, University of Coimbra. At the same time, CB integrated the team of other FCT-funded projects working on the search for new therapeutic strategies to circumvent the impairment of p53 pathway in human cancers. Within PhD, CB published 7 original articles, 2 as first author (Cell Death Dis and IJMS) and 5 as co-author (e.g., Oncotarget) in peer-reviewed international journals in oncology, as well as 1 book chapter in co-authorship (Elsevier). Her findings had translated into a national patent and an international patent request. She was also awarded with an EMBO/FEBS fellowship to present her results regarding the identification of the PKCd-selective activator at the prestigious 'The FEBS EMBO 2014 Conference'. Moreover, she co-supervised an undergraduate student and 2 MSc students, participated in the scientific jury of a MSc thesis, and was invited to teach lessons of Microbiology at Faculty of Pharmacy-UP. Her research was presented in 8 oral communications and 4 posters at national and international meetings, including International Conference on Cancer Research and Targeted Therapy. After completing PhD, CB moved to the National Institute of Health Dr. Ricardo Jorge - Lisbon, as researcher at the Jordan's group under the scope of a FTC-funded project. There, she extended her research to the study of inflammatory tumor microenvironment, and how it modulates the alternative splicing patterns in order to support the malignant progression of CRC. Interestingly, she was able to provide evidence that further supported the close association between inflammatory conditions and CRC development, and identify potential biomarkers and therapeutic targets for the prevention and/or treatment of CRC. She published an original article (Cancers), and an invited review (IJMS), in peer-reviewed international journals (both as first author). Finally, her work was presented at national and international meeting, such as 4th International Caparica Conference in SPLICING 2021 and Goodbye Flat Biology: Next Generation Cancer Models - EARC Conferences. Meanwhile, she successfully completed the Advanced Laboratory Animal Science Course – FELASA Functions A/B/D at i3S – University of Porto, which was essential for her experimental approach as it enabled her to carry out experimentation on animals. Last year, she embraced a project in the emerging topic of cancer immunology/glycobiology, and joined the Pinho's Lab also as researcher at i3S. Here, she explored the potential of aberrant CRC glycosylation as a novel immunotherapeutic strategy to prevent and/or treat CRC. In parallel, she developed an independent research line focused on the impact of glycans on circulating tumor cells biology, immune recognition and metastatic competence, and co-supervised a PhD student.
Identificação

Identificação pessoal

Nome completo
Cláudia Sofia Santos Bessa
Data de nascimento
1988/02/06
Género
Feminino

Nomes de citação

  • Bessa, Cláudia

Identificadores de autor

Ciência ID
B91A-7D4F-E3F1
ORCID iD
0000-0001-6240-2329

Endereços de correio eletrónico

  • claudiasantos26@gmail.com (Pessoal)

Telefones

Telemóvel
  • 919592108 (Pessoal)

Moradas

  • Rua Professor Sampaio de Carvalho, nº 124, Edifício Lante, 501, 4780-533, Santo Tirso, Santo Tirso, Portugal (Pessoal)

Domínios de atuação

  • Ciências Médicas e da Saúde - Medicina Clínica - Oncologia
  • Ciências Médicas e da Saúde - Medicina Básica - Imunologia
  • Ciências Naturais - Ciências Biológicas - Biologia Molecular
  • Ciências Naturais - Ciências Biológicas - Biologia Celular
  • Ciências Médicas e da Saúde - Medicina Básica - Farmacologia e Farmácia

Idiomas

Idioma Conversação Leitura Escrita Compreensão Peer-review
Português (Idioma materno)
Inglês Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1)
Formação
Grau Classificação
2024/05/13 - 2024/05/16
Concluído
Introduction to Python and Machine Learning for the Biosciences - 7 th Edition (Outros)
Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
2023/09/25 - 2023/09/28
Concluído
Workshop on Cancer Biology; Biological and Molecular Basis (Outros)
Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
20
2022/05/09 - 2022/05/20
Concluído
Laboratory Animal Science Course | XXXII edition - FELASA Functions A/B/D (Outros)
Especialização em Animal Sciences
Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
2013/04/01 - 2018/07/19
Concluído
Pharmaceutical Sciences (Doutoramento)
Especialização em Pharmacology and Pharmacotherapy
Universidade do Porto Faculdade de Farmácia, Portugal
"Targeted regulation of Protein kinase C (PKC) signaling pathway: Searching for new therapeutic strategies against cancer." (TESE/DISSERTAÇÃO)
Approved
2014/01/20 - 2014/02/07
Concluído
Essential Molecular Biology - A hands-on laboratory course (Outros)
Especialização em Molecular biology
Universidade do Porto Faculdade de Medicina, Portugal
2009/09/01 - 2012/02/01
Concluído
Molecular Genetics (Mestrado)
Universidade do Minho, Portugal
"Using yeast to study the role of ceramide pathway in the regulation of mammalian PKC isoforms." (TESE/DISSERTAÇÃO)
17
2006/09/01 - 2009/07/18
Concluído
Biology (Licenciatura)
Especialização em Investigation
Universidade do Porto Faculdade de Ciências, Portugal
14
Percurso profissional

Outros

Categoria Profissional
Instituição de acolhimento
Empregador
2023/03/01 - 2024/02/29 Junior researcher Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
2019/04/15 - 2022/04/30 Junior researcher FCiênciasID Associação para a Investigação e Desenvolvimento de Ciências, Portugal
FCiênciasID Associação para a Investigação e Desenvolvimento de Ciências, Portugal
2013/03/01 - 2018/07/19 PhD student Fundação para a Ciência e a Tecnologia, Portugal
Universidade do Porto Faculdade de Farmácia, Portugal
Projetos

Bolsa

Designação Financiadores
2016/01/01 - 2018/12/31 Targeting p53 family proteins: on the route to new anticancer agents
PTDC/DTPFTO/1981/2014
Bolseiro de Doutoramento
Universidade do Porto Faculdade de Farmácia, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2016/01 - 2018/12 Navigating through marine-derived fungi: bioprospection and synthesis of bioactive secondary metabolites and analogues as chemotherapic agents
PTDC/MARBIO/ 4694/2014
Bolseiro de Doutoramento
Universidade do Porto Faculdade de Farmácia, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011/04/01 - 2013/03/31 Functional, molecular and pharmacological studies of p53 family proteins: from yeast to human cells.
Technician
Universidade do Porto Faculdade de Farmácia, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011/01 - 2013/03 Novel canine norovirus: molecular, epidemiologic and pathogenic aspects.
Technician
Universidade do Porto Faculdade de Farmácia, Portugal
Fundação para a Ciência e a Tecnologia
Concluído

Projeto

Designação Financiadores
2023/03/01 - 2024/02/29 The Glyco-Immuno Code in Colorectal Cancer: An opportunity for novel Immunotherapeutic Strategies for Cancer Prevention.
No reference
Investigador
Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
Em curso
2019/04/15 - 2021/10/14 Microenvironmental effects on alternative splicing in malignant progression of colorectal tumor cells.
PTDC/BIA-MOL/28386/2017
Investigador
Fundação da Faculdade de Ciências da Universidade de Lisboa, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
Produções

Publicações

Artigo em revista
  1. Bessa, Cláudia; Loureiro, Joana B.; Barros, Matilde; Isca, Vera M. S.; Sardão, Vilma A.; Oliveira, Paulo J.; Bernardino, Raquel L.; et al. "Counteracting Colon Cancer by Inhibiting Mitochondrial Respiration and Glycolysis with a Selective PKCd Activator". International Journal of Molecular Sciences 24 6 (2023): 5710. http://dx.doi.org/10.3390/ijms24065710.
    Acesso aberto • 10.3390/ijms24065710
  2. Pereira, Joana F. S.; Bessa, Cláudia; Matos, Paulo; Jordan, Peter. "Pro-Inflammatory Cytokines Trigger the Overexpression of Tumour-Related Splice Variant RAC1B in Polarized Colorectal Cells". Cancers 14 6 (2022): 1393. http://dx.doi.org/10.3390/cancers14061393.
    Acesso aberto • Publicado • 10.3390/cancers14061393
  3. Bessa, Cláudia; Matos, Paulo; Jordan, Peter; Gonçalves, Vânia. "Alternative Splicing: Expanding the Landscape of Cancer Biomarkers and Therapeutics". International Journal of Molecular Sciences 21 23 (2020): 9032. http://dx.doi.org/10.3390/ijms21239032.
    10.3390/ijms21239032
  4. Garcia, Catarina; Ntungwe, Epole; Rebelo, Ana; Bessa, Cláudia; Stankovic, Tijana; Dinic, Jelena; Díaz-Lanza, Ana; et al. "Parvifloron D from Plectranthus strigosus: Cytotoxicity Screening of Plectranthus spp. Extracts.". Biomolecules 9 10 (2019): 616. http://dx.doi.org/10.3390/biom9100616.
    Publicado • 10.3390/biom9100616
  5. Bessa, Cláudia; Soares, Joana; Raimundo, Liliana; Loureiro, Joana B.; Gomes, Célia; Reis, Flávio; Soares, Miguel L.; et al. "Discovery of a small-molecule protein kinase Cd-selective activator with promising application in colon cancer therapy". Cell Death & Disease 9 2 (2018): http://dx.doi.org/10.1038/s41419-017-0154-9.
    10.1038/s41419-017-0154-9
  6. Soares, Joana; Raimundo, Liliana; Pereira, Nuno A.L.; Monteiro, Ângelo; Gomes, Sara; Bessa, Cláudia; Pereira, Clara; et al. "Reactivation of wild-type and mutant p53 by tryptophanolderived oxazoloisoindolinone SLMP53-1, a novel anticancer small-molecule.". Oncotarget 7 4 (2015): http://dx.doi.org/10.18632/oncotarget.6775.
    Publicado • 10.18632/oncotarget.6775
  7. Leão, Mariana; Soares, Joana; Gomes, Sara; Raimundo, Liliana; Ramos, Helena; Bessa, Cláudia; Queiroz, Glória; et al. "Enhanced cytotoxicity of prenylated chalcone against tumour cells via disruption of the p53–MDM2 interaction.". Life Sciences 142 (2015): 60-65. http://dx.doi.org/10.1016/j.lfs.2015.10.015.
    Publicado • 10.1016/j.lfs.2015.10.015
  8. Oliveira, Manuela; Pereira, Clara; Bessa, Cláudia; Araujo, Ricardo; Saraiva, Lucília. "Chronological aging in conidia of pathogenic Aspergillus : Comparison between species.". Journal of Microbiological Methods 118 (2015): 57-63. http://dx.doi.org/10.1016/j.mimet.2015.08.021.
    Publicado • 10.1016/j.mimet.2015.08.021
  9. Soares, Joana; Pereira, Nuno A.L.; Monteiro, Ângelo; Leão, Mariana; Bessa, Cláudia; dos Santos, Daniel J.V.A.; Raimundo, Liliana; et al. "Oxazoloisoindolinones with in vitro antitumor activity selectively activate a p53-pathway through potential inhibition of the p53–MDM2 interaction.". European Journal of Pharmaceutical Sciences 66 (2015): 138-147. http://dx.doi.org/10.1016/j.ejps.2014.10.006.
    Publicado • 10.1016/j.ejps.2014.10.006
  10. Leão, Mariana; Gomes, Sara; Bessa, Cláudia; Soares, Joana; Raimundo, Liliana; Monti, Paola; Fronza, Gilberto; Pereira, Clara; Saraiva, Lucília. "Studying p53 family proteins in yeast: Induction of autophagic cell death and modulation by interactors and small molecules.". Experimental Cell Research 330 1 (2015): 164-177. http://dx.doi.org/10.1016/j.yexcr.2014.09.028.
    Publicado • 10.1016/j.yexcr.2014.09.028
  11. Oliveira, M.; Pereira, C.; Bessa, C.; Araujo, R.; Saraiva, L.. "Hydrogen peroxide-induced secondary necrosis in conidia of Aspergillus fumigatus". Canadian Journal of Microbiology 62 2 (2015): 95-101. http://www.scopus.com/inward/record.url?eid=2-s2.0-84956669792&partnerID=MN8TOARS.
    10.1139/cjm-2015-0561
  12. Bessa, Cláudia; Pereira, Clara; Leão, Mariana; Maciel, Cláudia; Gomes, Sara; Gonçalves, Jorge; Corte-Real, Manuela; Costa, Vítor; Saraiva, Lucília. "Using yeast to uncover the regulation of protein kinase Cd by ceramide". FEMS Yeast Research 13 7 (2013): 700-705. http://dx.doi.org/10.1111/1567-1364.12069.
    10.1111/1567-1364.12069
  13. Leão, Mariana; Gomes, Sara; Soares, Joana; Bessa, Cláudia; Maciel, Cláudia; Ciribilli, Yari; Pereira, Clara; Inga, Alberto; Saraiva, Lucília. "Novel simplified yeast-based assays of regulators of p53-MDMX interaction and p53 transcriptional activity". FEBS Journal 280 24 (2013): 6498-6507. http://www.scopus.com/inward/record.url?eid=2-s2.0-84885971948&partnerID=MN8TOARS.
    10.1111/febs.12552
  14. Pereira, Clara; Leao, Mariana; Soares, Joana; Bessa, Cláudia; Saraiva, Lucilia. "New Therapeutic Strategies for Cancer and Neurodegeneration Emerging from Yeast Cell-based Systems.". Current Pharmaceutical Design 18 27 (2012): 4223-4235. http://dx.doi.org/10.2174/138161212802430422.
    Publicado • 10.2174/138161212802430422
  15. Pereira, Clara; Bessa, Cláudia; Saraiva, Lucília. "Endocytosis inhibition during H2O2-induced apoptosis in yeast.". FEMS Yeast Research 12 7 (2012): 755-760. http://dx.doi.org/10.1111/j.1567-1364.2012.00825.x.
    Publicado • 10.1111/j.1567-1364.2012.00825.x
  16. Pereira, Clara; Coutinho, Isabel; Soares, Joana; Bessa, Cláudia; Leão, Mariana; Saraiva, Lucília. "New insights into cancer-related proteins provided by the yeast model.". FEBS Journal 279 5 (2012): 697-712. http://dx.doi.org/10.1111/j.1742-4658.2012.08477.x.
    Publicado • 10.1111/j.1742-4658.2012.08477.x
  17. Pereira, Clara; Bessa, Cláudia; Soares, Joana; Leão, Mariana; Saraiva, Lucília. "Contribution of Yeast Models to Neurodegeneration Research.". Journal of Biomedicine and Biotechnology 2012 (2012): 1-12. http://dx.doi.org/10.1155/2012/941232.
    Publicado • 10.1155/2012/941232
Artigo em revista (magazine)
  1. Soares, Joana; Leão, Mariana; Bessa, Cláudia; Gomes, Sara; Maciel, Cláudia; Raimundo, Liliana; Harilal, Nilma; Saraiva, Lucília. "Humanized yeast: in the front line of anticancer drug discovery.", Portuguese Society for Microbiology Magazine, 2012, https://spmicrobiologia.files.wordpress.com/2013/12/2013129-12b.pdf.
Capítulo de livro
  1. Matias, D.; Bessa, C.; Fátima Simões, M.; Reis, C.P.; Saraiva, L.; Rijo, P.. "Natural Products as Lead Protein Kinase C Modulators for Cancer Therapy". 45-79. 2016.
    10.1016/B978-0-444-63749-9.00002-5
Poster em conferência
  1. Bessa, Cláudia. "A pro-inflammatory microenvironment triggers overexpression of tumor-related RAC1B in polarized colorectal cancer cells.". Trabalho apresentado em The Structural Microenvironment: Breaking down the walls of cancer. EARC Conferences, 2022.
  2. Bessa, Cláudia. "A pro-inflammatory microenvironment triggers overexpression of tumor-related RAC1B in polarized colorectal cancer cells.". Trabalho apresentado em Goodbye Flat Biology: Next Generation Cancer Models. EARC Conferences, 2021.
  3. Bessa, Cláudia. "Targeting tumour-related alternative splice variant RAC1B with anti-sense oligonucleotides.". Trabalho apresentado em 1 st Symposium on Oligonucleotide Technologies and Therapeutics@Portugal, 2021.
  4. Rijo, Patrícia; Vera M. S. Isca; Epole Ntungwe N; Domínguez-Martín EM; Bessa, Cláudia; Lucília Saraiva; Carlos A.M. Afonso. "Abietane diterpenoids from Plectranthus spp. as a New Class of Protein Kinase C Modulators for Cancer Therapy". Trabalho apresentado em Physioma 2019, 2019.
  5. Bessa, Cláudia. "Exploring the antitumor potential of abietane derivatives through Mitsunobu reaction.". Trabalho apresentado em FMC International Symposium on Advances in Synthetic and Medicinal Chemistry, 2017.
  6. Soares, Joana; Raimundo, Liliana; Pereira, Nuno; Monteiro, Ângelo; Gomes, Ana Sara; Gomes, Sara; Bessa, Cláudia; et al. "Reactivation of mutant p53R280K by SLMP53-1, a potential anticancer drug candidate". Trabalho apresentado em XIX National Congress of Biochemistry, 2016.
  7. Bessa, Cláudia; Soares, Joana; Raimundo, Liliana; Fernandes, Bryan; Gomes, Célia; Reis, Flávio; Soares, Miguel Luz; et al. "Roy-Bz: a new small-molecule selective activator of protein kinase Cd with anticancer activity.". Trabalho apresentado em International Conference on Cancer Research and Targeted Therapy, 2016.
  8. Bessa, Cláudia. "Prenylated chalcones with enhanced cytotoxicity against tumor cells through disruption of the p53-MDM2 interaction.". Trabalho apresentado em EACR Conference Series, 2016.
  9. Bessa, Cláudia. "SLMP53-1: A new small-molecule reactivator of p53 with promising antitumor properties.". Trabalho apresentado em EACR Conference Series, 2016.
  10. Bessa, Cláudia; Harilal, Nilma; Pereira, Clara; Maciel, Cláudia; Gonçalves, Jorge; Rijo, Patrícia; Simões, Maria de Fátima; Saraiva, Lucília. "A selective activator of protein kinase Cd discovered using yeast.". Trabalho apresentado em FEBS EMBO, 2014.
  11. Bessa, Cláudia; Pereira, Clara; Maciel, Cláudia; Gonçalves, Jorge; Rijo, Patrícia; Simões, Maria de Fátima; Saraiva, Lucília. "A selective activator of protein kinase Cd identified using yeast.". Trabalho apresentado em 26th International Conference on yeast genetics and molecular biology, 2013.
  12. Bessa, Cláudia; Pereira, Clara; Machado, Joana; Gonçalves, Jorge; Rijo, Patrícia; Simões, Maria de Fátima; Saraiva, Lucília. "Using yeast to search for new selective activators of protein kinase C isoforms.". Trabalho apresentado em IJUP6th meeting of young researchers, 2013.
  13. Bessa, Cláudia. "A new inhibitor of p53-MDM2 interaction discovered using a yeast target-based screening approach.". Trabalho apresentado em 6º Encontro de Investigação Jovem da Universidade do Porto (IJUP), 2013.
    10.1158/1538-7445.am2014-1645
  14. Bessa, Cláudia. "NAP's: potencia lactivators of p53 activity identified using yeast cell-based screening assays.". Trabalho apresentado em 3ºEncontro Nacional de Química Terapêutica, 2012.
  15. Bessa, Cláudia. "Discovery of a new inhibitor of p53-MDM2 interaction using a yeast target-based screening strategy.". Trabalho apresentado em 20th Euroconference on Apoptosis “From Death to Eternity", 2012.
    10.1158/1538-7445.am10-4529
  16. Bessa, Cláudia; Leão, M.; Gonçalves, Jorge; Côrte-Real, Manuela; Costa, Vítor; Saraiva, Lucília. "Using yeast to study the regulation of mammalian protein kinase c isoforms by the ceramide pathway". Trabalho apresentado em XIX Jornadas de Biologia de Leveduras “Professor Nicolau van Uden”, 2012.
Resumo em conferência
  1. Bessa, C; Pereira, C; Maciel, C; Goncalves, J; Rijo, P; Simoes, M; Saraiva, L; et al. "A selective activator of protein kinase Cdelta identified using yeast". Trabalho apresentado em FEBS EMBO, Paris, 2013.
    Publicado

Propriedade Intelectual

Patente
  1. Bessa, Cláudia; Soares, Joana; Raimundo, Liliana; Gonçalves, Jorge; Simões, Maria de Fátima; Rijo, Patrícia; Saraiva, Lucília. 2017. "A small-molecule selective activator of protein kinase Cdelta.". Portugal.
    Expirada
Atividades

Apresentação oral de trabalho

Título da apresentação Nome do evento
Anfitrião (Local do evento)
2021/07/26 Exploring the effect of the pro-inflammatory microenvironment on the expression of the tumor-related RAC1B splice variant in colorectal cancer cells. 4th International Caparica Conference in SPLICING 2021
(Caparica, Portugal)
2021/07/08 Targeting tumour-related alternative splice variant RAC1B with anti-sense oligonucleotides. 1 st Symposium on Oligonucleotide Technologies and Therapeutics@Portugal,
(Portugal)
2017/02/02 Targeting colon cancer with the selective PKCd activator Roy-Bz. XLVII Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXV Reunião de Farmacologia Clínica, XVI Reunião de Toxicologia
(Coimbra, Portugal)
2016/12/08 A small-molecule selective activator of protein kinase Cd with anticancer properties. XIX National Congress of Biochemistry
(Guimarães, Portugal)
2016/02/04 The diterpenoid Roy-Bz: first small-molecule selective activator of protein kinase Cd. XLVI Reunião da Sociedade Portuguesa de Farmacologia, XXXIV Reunião de Farmacologia Clínica, XV Reunião de Toxicologia
(Porto, Portugal)
2015/12/01 Roy-Bz: the first small-molecule selective activator of protein Kinase Cd. 11º Encontro Nacional de Química Orgânica / 4º Encontro Nacional de Química Terapêutica
(Porto, Portugal)
2015/12/01 SLMP53-1: a new reactivator of mutant p53 with potent in vivo antitumor activity. 11º Encontro Nacional de Química Orgânica/4º Encontro Nacional de Química Terapêutica
(Porto, Portugal)
2015/07/13 Tryptophanolderived oxazoloisoindolinone reactivators of mutant p53. ISBIO (integrative structural biology tools for the study of proteiligand interactions)
(Lisboa, Portugal)
2015/02/04 Identification of a selective small-molecule activator of PKCd with potential antitumor properties. XLV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXIII Reunião de Farmacologia Clínica e XIV Reunião de Toxicologia
(Lisboa, Portugal)
2015/02/04 A new inhibitor of the p53-MDM2 interaction derived from naturally occurring chalcones. XLV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXIII Reunião de Farmacologia Clínica e XIV Reunião de Toxicologia
(Lisboa, Portugal)
2015/02/04 SLMP531: a new reactivator of mutant p53 with potente antitumor activity. XLV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXIII Reunião de Farmacologia Clínica e XIV Reunião de Toxicologia
(Lisboa, Portugal)
2015/02/04 Novel yeast-based approaches to search for inhibitors of the interaction of p53 family proteins with MDM2/MDMX. XLV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXIII Reunião de Farmacologia Clínica e XIV Reunião de Toxicologia
(Lisboa, Portugal)
2015/02/04 Identification of a selective small-molecule activator of PKCd with potential antitumor properties. XLV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXIII Reunião de Farmacologia Clínica e XIV Reunião de Toxicologia
(Lisboa, Portugal)
2014/07/11 A selective activator of protein kinase Cd discovered using a yeast-based assay. XIII Jornadas de Biologia de Leveduras “Professor Nicolau van Uden”
(Lisboa, Portugal)
2014/02/12 A new selective activator of PKCd discovered using a yeast-based assay. IJUP7th meeting of young researchers
(Porto, Portugal)
2014/02/12 Discovery of a new small-molecule inhibitor of the p53-MDM2 interaction. IJUP7th meeting of young researchers
(Porto, Portugal)
2014/02/05 A novel selective small-molecule activator of protein kinase Cd. XLIV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXII Reunião de Farmacologia Clínica e XIII Reunião de Toxicologia
(Coimbra, Portugal)
2014/02/05 A new small-molecule activator of wild-type and mutant p53 with potential antitumor properties. XLIV Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXII Reunião de Farmacologia Clínica e XIII Reunião de Toxicologia
(Coimbra, Portugal)
2013/02/06 Identification of potential activators of p53 activity using yeast-based screening assays. XLIII Reunião Anual da Sociedade Portuguesa de Farmacologia, XXXI Reunião de Farmacologia Clínica e XII Reunião de Toxicologia
(Porto, Portugal)
2012/06/15 A new inhibitor of p53-MDM2 interaction discovered using a yeast targetbased screening approach. XIX Jornadas de Biologia de Leveduras “Professor Nicolau van Uden”
(Lisboa, Portugal)

Orientação

Título / Tema
Papel desempenhado
Curso (Tipo)
Instituição / Organização
2011/09/01 - 2012/10/31 Estudos funcionais e farmacológicos de mutantes da proteína p53 humana utilizando a levedura como modelo celular.
Coorientador
Ciências Farmacêuticas (Licenciatura/Bacharelato)
Universidade do Porto Faculdade de Farmácia, Portugal

Participação em evento

Descrição da atividade
Tipo de evento
Nome do evento
Instituição / Organização
2020/07/13 - 2020/07/16 Splicing 2020 intends to join in a friendly academic environment all that work or are interested in the area of alternative splicing research.
Conferência
3rd International Caparica Conference in Splicing 2020
2019/10/18 - 2019/10/19 The SINAL is a meeting about signal transduction pathways with the aim of fostering collaborations and interactions promoting science.
Encontro
SINAL 2019 - 10th meeting of Signal Transduction

Júri de grau académico

Tema
Tipo de participação
Nome do candidato (Tipo de grau)
Instituição / Organização
2014/11/20 Searching for inhibitors of the p53 interaction with MDM2 and MDMX: from yeast to human cells.
Arguente
Helena Rocha (Mestrado)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Curso / Disciplina lecionado

Disciplina Curso (Tipo) Instituição / Organização
2015/09/24 - 2015/09/24 Microbiology theoretical classes. Ciências Farmacêuticas (Mestrado integrado) Universidade do Porto Faculdade de Farmácia, Portugal
2014/09/28 - 2014/09/28 Microbiology theoretical classes. Ciências Farmacêuticas (Mestrado integrado) Universidade do Porto Faculdade de Farmácia, Portugal
2014/09/27 - 2014/09/27 Microbiology pratical classes. Ciências Farmacêuticas (Mestrado integrado) Universidade do Porto Faculdade de Farmácia, Portugal
Distinções

Prémio

2014 Fellowship FEBS (Federation of European Biochemical Societies)
Federation of European Biochemical Societies, Reino Unido