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Biography

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. 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-UCoimbra. Meanwhile, she 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 PKCdelta-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 practical 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 Post-Doc at the Jordan¿s group (Oncobiology and Signaling Pathways Lab) under the scope of an FTC-funded project. There, she carried out a work aiming to study the inflammatory tumor microenvironment, and how it modulates the alternative splicing patterns in order to support the malignant progression of colon cancer. During the Post-Doc, 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. Recently, she decided to develop a second Post-Doc in cancer immunology/glycobiology and joined the Pinho¿s Lab (Immunology, Cancer & Glycomedicine group) at i3S-UP. She is currently exploring the potential of aberrant CRC glycosylation as a novel immunotherapeutic strategy to CRC prevention. In parallel, she is developing an independent research line focused on the impact of glycans on CTC biology, immune recognition and metastatic competence, and co-supervising a PhD student. Overall, until now, CB has 17 publications in peer-reviewed international journals, with a total of 456 citations, with a h-index of 11 and an accumulated impact factor of 63,34.

Activities

Employment (2)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto: Porto, PT

2023-03-01 to present | Junior Researcher (Immunology, Cancer & GlycoMedicine group)
Employment
Source: Self-asserted source
Bessa, C.

Fundação da Faculdade de Ciências da Universidade de Lisboa: Lisboa, Lisboa, PT

2019-04-15 to 2021-10-14 | Contracted Researcher
Employment
Source: Self-asserted source
Bessa, C.

Education and qualifications (3)

Universidade do Porto Faculdade de Farmácia: Porto, Porto, PT

2013-04-01 to 2017-07-19 | Doutoramento (Famacologia e Farmacoterapia)
Education
Source: Self-asserted source
Bessa, C.

Universidade do Minho: Braga, Braga, PT

2009-09-01 to 2012-02-01 | Mestrado (Genética Molecular)
Education
Source: Self-asserted source
Bessa, C.

Universidade do Porto Faculdade de Ciências: Porto, Porto, PT

2006-09-01 to 2009-07-18 | Licenciatura (Biologia)
Education
Source: Self-asserted source
Bessa, C.

Funding (5)

Microenvironmental effects on alternative splicing in malignant progression of colorectal tumor cells

2019-04 to 2021-10 | Contract
Fundação para a Ciência e a Tecnologia (Lisboa, PT)
Part of GRANT_NUMBER:

PTDC/BIA-MOL/28386/2017

Source: Self-asserted source
Bessa, C.

Navigating through marine-derived fungi: bioprospection and synthesis of bioactive secondary metabolites and analogues as chemotherapic agents

2016-01 to 2018-12 | Grant
Fundação para a Ciência e a Tecnologia (Lisboa, PT)
GRANT_NUMBER:

PTDC/MARBIO/ 4694/2014

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Targeting p53 family proteins: on the route to new anticancer agents

2016-01 to 2018-12 | Grant
Fundação para a Ciência e a Tecnologia (Lisboa, PT)
GRANT_NUMBER:

PTDC/DTPFTO/1981/2014

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Functional, molecular and pharmacological studies of p53 family proteins: from yeast to human cells.

2011-04 to 2013-03 | Grant
Fundação para a Ciência e a Tecnologia (Lisboa, PT)
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Novel canine norovirus: molecular, epidemiologic and pathogenic aspects.

2011-01 to 2013-03 | Grant
Fundação para a Ciência e a Tecnologia (Lisboa, PT)
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Works (39)

Counteracting Colon Cancer by Inhibiting Mitochondrial Respiration and Glycolysis with a Selective PKCδ Activator

International Journal of Molecular Sciences
2023-03 | Journal article | Author
Contributors: Bessa, C.; Joana B. Loureiro; Matilde Barros; Vera M. S. Isca; Vilma A. Sardão; Paulo J. Oliveira; Raquel Bernardino; Carina Herman-de-Sousa; Costa, M.A.; Paulo Correia-de-Sá et al.
Source: check_circle
Multidisciplinary Digital Publishing Institute
grade
Preferred source (of 3)‎

Pro-Inflammatory Cytokines Trigger the Overexpression of Tumour-Related Splice Variant RAC1B in Polarized Colorectal Cells

Cancers
2022-03-09 | Journal article
SOURCE-WORK-ID:

cv-prod-id-3079751

Contributors: Pereira, Joana F. S.; Bessa, Cláudia; Matos, Paulo; Jordan, Peter
Source: check_circle
CIÊNCIAVITAE

A pro-inflammatory microenvironment triggers overexpression of tumor-related RAC1B in polarized colorectal cancer cells.

The Structural Microenvironment: Breaking down the walls of cancer. EARC Conferences
2022-02-22 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-3421406

Contributors: Bessa, Cláudia
Source: check_circle
CIÊNCIAVITAE

A pro-inflammatory microenvironment triggers overexpression of tumor-related RAC1B in polarized colorectal cancer cells.

Goodbye Flat Biology: Next Generation Cancer Models. EARC Conferences
2021-10-05 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-3421416

Contributors: Bessa, Cláudia
Source: check_circle
CIÊNCIAVITAE

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
2021-07-26 | Conference abstract
Contributors: Bessa, C.
Source: Self-asserted source
Bessa, C.

Targeting tumour-related alternative splice variant RAC1B with anti-sense oligonucleotides.

1 st Symposium on Oligonucleotide Technologies and Therapeutics@Portugal
2021-07-08 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-3421369

Contributors: Bessa, Cláudia
Source: check_circle
CIÊNCIAVITAE

Targeting tumour-related alternative splice variant RAC1B with anti-sense oligonucleotides.

1st Symposium on Oligonucleotide Technologies and Therapeutics@Portugal
2021-07-08 | Conference poster
Contributors: Bessa, C.
Source: Self-asserted source
Bessa, C.

Alternative Splicing: Expanding the Landscape of Cancer Biomarkers and Therapeutics

International Journal of Molecular Sciences
2020-12 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Abietane diterpenoids from Plectranthus spp. as a New Class of Protein Kinase C Modulators for Cancer Therapy

Physioma 2019
2019-10 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-4238097

Contributors: Rijo, Patrícia; Vera M. S. Isca; Epole Ntungwe N; Domínguez-Martín EM; Bessa, Cláudia; Lucília Saraiva; Carlos A.M. Afonso
Source: check_circle
CIÊNCIAVITAE

Parvifloron D from Plectranthus strigosus: Cytotoxicity Screening of Plectranthus spp. Extracts

Biomolecules
2019-10 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 5)‎

Discovery of a small-molecule protein kinase Cd-selective activator with promising application in colon cancer therapy.

Cell Death & Disease
2018-01-18 | Journal article
SOURCE-WORK-ID:

cv-prod-id-992499

Part of ISSN: 2041-4889
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Exploring the antitumor potential of abietane derivatives through Mitsunobu reaction.

FMC International Symposium on Advances in Synthetic and Medicinal Chemistry
2017-08-27 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1412037

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

A small-molecule selective activator of protein kinase Cdelta.

2017-02-06 | Patent
SOURCE-WORK-ID:

cv-prod-id-992565

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Natural Products as Lead Protein Kinase C Modulators for Cancer Therapy.

Studies in Natural Products Chemistry
2016 | Book chapter
SOURCE-WORK-ID:

cv-prod-id-992534

Part of ISSN: 1572-5995
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Reactivation of mutant p53R280K by SLMP53-1, a potential anticancer drug candidate

XIX National Congress of Biochemistry
2016-12-09 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-4238109

Contributors: Soares, Joana; Raimundo, Liliana; Pereira, Nuno; Monteiro, Ângelo; Gomes, Ana Sara; Gomes, Sara; Bessa, Cláudia; et al.
Source: check_circle
CIÊNCIAVITAE

Roy-Bz: a new small-molecule selective activator of protein kinase Cd with anticancer activity.

International Conference on Cancer Research and Targeted Therapy
2016-10-21 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1006028

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Prenylated chalcones with enhanced cytotoxicity against tumor cells through disruption of the p53-MDM2 interaction.

EACR Conference Series
2016-01-28 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1412064

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

SLMP53-1: A new small-molecule reactivator of p53 with promising antitumor properties.

EACR Conference Series
2016-01-28 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1412088

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Hydrogen peroxide-induced secondary necrosis in conidia of Aspergillus fumigatus

Canadian Journal of Microbiology
2015 | Journal article
EID:

2-s2.0-84956669792

Part of ISSN: 14803275 00084166
Contributors: Oliveira, M.; Pereira, C.; Bessa, C.; Araujo, R.; Saraiva, L.
Source: Self-asserted source
Bessa, C. via Scopus - Elsevier
grade
Preferred source (of 2)‎

Enhanced cytotoxicity of prenylated chalcone against tumour cells via disruption of the p53–MDM2 interaction.

Life Sciences
2015-12 | Journal article
SOURCE-WORK-ID:

cv-prod-id-992505

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Reactivation of wild-type and mutant p53 by tryptophanolderived oxazoloisoindolinone SLMP53-1, a novel anticancer small-molecule.

Oncotarget
2015-12-28 | Journal article
SOURCE-WORK-ID:

cv-prod-id-992504

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Chronological aging in conidia of pathogenic Aspergillus : Comparison between species.

Journal of Microbiological Methods
2015-11 | Journal article
SOURCE-WORK-ID:

cv-prod-id-992507

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Oxazoloisoindolinones with in vitro antitumor activity selectively activate a p53-pathway through potential inhibition of the p53–MDM2 interaction.

European Journal of Pharmaceutical Sciences
2015-01 | Journal article
SOURCE-WORK-ID:

cv-prod-id-992515

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Studying p53 family proteins in yeast: Induction of autophagic cell death and modulation by interactors and small molecules.

Experimental Cell Research
2015-01 | Journal article
SOURCE-WORK-ID:

cv-prod-id-992520

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

A selective activator of protein kinase Cd discovered using yeast.

FEBS EMBO
2014-08-30 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1006778

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

A selective activator of protein kinase Cdelta identified using yeast

FEBS EMBO
2013 | Conference abstract
SOURCE-WORK-ID:

cv-prod-id-4238100

Part of ISSN: 0749-503X
AUTHENTICUSID: P-006-JXB
WOSUID:

WOS:000327927400435

WOSUID:

WOS:000359666803007

Contributors: Bessa, C; Pereira, C; Maciel, C; Goncalves, J; Rijo, P; Simoes, M; Saraiva, L; et al.
Source: check_circle
CIÊNCIAVITAE

Novel simplified yeast-based assays of regulators of p53-MDMX interaction and p53 transcriptional activity

FEBS Journal
2013 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Using yeast to uncover the regulation of protein kinase Cδ by ceramide

FEMS Yeast Research
2013 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

A selective activator of protein kinase Cd identified using yeast.

26th International Conference on yeast genetics and molecular biology
2013-08-29 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1006827

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

A new inhibitor of p53-MDM2 interaction discovered using a yeast target-based screening approach.

6º Encontro de Investigação Jovem da Universidade do Porto (IJUP)
2013-02-13 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1412133

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Using yeast to search for new selective activators of protein kinase C isoforms.

IJUP6th meeting of young researchers
2013-02-13 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1006838

Contributors: Bessa, Cláudia; Pereira, Clara; Machado, Joana; Gonçalves, Jorge; Rijo, Patrícia; Simões, Maria de Fátima; Saraiva, Lucília
Source: check_circle
CIÊNCIAVITAE

Contribution of yeast models to neurodegeneration research

Journal of Biomedicine and Biotechnology
2012 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Endocytosis inhibition during H 2O 2-induced apoptosis in yeast

FEMS Yeast Research
2012 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

New insights into cancer-related proteins provided by the yeast model

FEBS Journal
2012 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

New therapeutic strategies for cancer and neuro degeneration emerging from yeast cell-based systems

Current Pharmaceutical Design
2012 | Journal article
Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

Humanized yeast: in the front line of anticancer drug discovery.

Portuguese Society for Microbiology Magazine
2012-12-20 | Magazine article
SOURCE-WORK-ID:

cv-prod-id-1004134

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Discovery of a new inhibitor of p53-MDM2 interaction using a yeast target-based screening strategy.

3º Encontro Nacional de Química Terapêutica
2012-11-28 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1412180

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 3)‎

NAP's: potencia lactivators of p53 activity identified using yeast cell-based screening assays.

3ºEncontro Nacional de Química Terapêutica
2012-11-28 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-1412250

Source: Self-asserted source
Bessa, C.
grade
Preferred source (of 2)‎

Using yeast to study the regulation of mammalian protein kinase c isoforms by the ceramide pathway

XIX Jornadas de Biologia de Leveduras “Professor Nicolau van Uden”
2012-06-15 | Conference poster
SOURCE-WORK-ID:

cv-prod-id-4238090

Contributors: Bessa, Cláudia; Leão, M.; Gonçalves, Jorge; Côrte-Real, Manuela; Costa, Vítor; Saraiva, Lucília
Source: check_circle
CIÊNCIAVITAE