Dott.ssa Desiana Somale
- f502-c003 Dottorato in Medicina Molecolare
- Dottorato: 29° ciclo
- Matricola: 706598
Contatti
- dsomale@unito.it
- Istituto di Candiolo - IRCCS
Istituto di Ricovero e Cura a Carattere Scientifico
Strada Provinciale, 142 km 3,95
10060 Candiolo, Torino-Italy - https://dott-mm.campusnet.unito.it/do/studenti.pl/Show?706598
- VCard contatti
- QRcode contatti
Supervisore
Federica CavalloTesi di dottorato
UNIVERSITA' degli STUDI di TORINO
Dipartimento di Scienze della Vita e Biologia dei Sistemi
Laurea Magistrale in Biologia Cellulare e Molecolare
Anno Accademico 2012-2013
Titolo della Tesi: INHIBITION OF PDK1 SIGNALING REDUCES ANCHORAGE-INDEPENDENT GROWTH OF COLON CANCER CELLS
Relatore: Prof. Luca PRIMO
Controrelatore: Prof.ssa Daniela TAVERNA
TESI di DOTTORATO in Medicina Molecolare (XXIX ciclo) dal titolo:
PDK1 targeting in mutated KRAS metastatic colorectal cancer
Attività di ricerca
- Projects
- Articles
- Oral Presentations
- Poster presentations
- Congresses
- Attended Progress Report
- Seminars
Progetti in corso:
1) Ruolo della via segnalazione PDK1-RSK nella crescita e nella sopravvivenza del carcinoma colon-rettale (CRC)
Le chinasi PDK1 e RSK sono coinvolte nel signaling intracellulare. Abbiamo dimostrato che l'inibizione della via di segnalazione di PDK1 riduce la crescita ancoraggio-indipendente delle cellule di carcinoma colon-rettale e la crescita degli organoidi derivati da pazienti. Questa inibizione correla con quella della chinasi RSK, uno degli effettori di PDK1. Il nostro scopo è quindi quello di dimostrare la presenza di un asse PDK1-RSK coinvolto nel carcinoma colon-rettale. I meccanismi di attivazione e inibizione di RSK non sono, però, ancora chiari. Un altro nostro obiettivo è dunque quello di caratterizzare, mediante l'utilizzo di mutanti funzionali, i meccanismi di regolazione intramolecolare dell'attività chinasica di RSK, nello specifico di RSK2.
2) Creazione di una piattaforma in vitro di organoidi ottenuti da xenopazienti di metastasi colon-rettali
In questi anni, nell'Istituto di Candiolo, è stato messo a punto un nuovo approccio per studiare il CRC metastatico basato sui PDX, porzioni di metastasi epatiche di CRC umani trapiantate in topo. Noi abbiamo recentemente iniziato a mantenere e propagare in vitro in cultura tridimensionale (3D) linee cellulari di CRC derivate da questi PDX. Il nostro scopo è quello di creare una piattaforma di organoidi in 3D in vitro che possa complementare quella dei PDX in vivo. Attualmente abbiamo in coltura sei linee cellulari derivate da xenopazienti. Queste linee mostrano una struttura ben organizzata, caratterizzata da un epitelio monostratificato che si ripiega per formare cripte e lumi, molto simile al fenotipo del colon. Questa piattaforma potrebbe essere utile per testare nuove combinazioni di farmaci, le quali potrebbero essere successivamente applicate sui pazienti.
3) Un approccio traslazionale per il CRC metastatico: studio sul differenziamento delle xenosfere
Il carcinoma colon-rettale è una delle neoplasia diagnosticate con maggiore frequenza nel mondo. Le vie di segnalazione maggiormente coinvolte nella patogenesi del CRC sono quelle attivate a valle del recettore per il fattore di crescita dell'epidermide (EGFR), quali RAS/MAPK e PI3K/AKT. Dai PDX di CRC sviluppati nel nostro Istituto è possibile isolare le cellule staminali, coltivandoli in sospensione con un terreno selettivo, e ottenere le cosiddette "xenosfere". PDX e xenosfere mostrano un fenotipo molto simile a quello del tumore originario. Sono quindi un buon modello per studiare nuovi approcci terapeutici per il trattamento del CRC. Una delle terapie utilizzate prevede l'inibizione dell'EGFR, mediante la somministrazione di anticorpi monoclonali (mAb) come, per esempio, il cetuximab (CTX). Studi clinici hanno però dimostrato che queste terapie sono del tutto inattive in pazienti con CRC il cui tumore presenta mutazioni in RAS o altre proteine coinvolte nelle vie di segnalazione a valle dell'EGFR. PDX trattati con la terapia anti-EGFR hanno risposto in modo differente: il 59,6% dei tumori non ha risposto e ha continuato a crescere; il 29,8% dei tumori ha smesso di crescere mantenendo le dimensioni originarie; mentre il 10,6% ha risposto diminuendo notevolmente di dimensioni. In quest'ultimo caso, il tumore non scompare mai del tutto. La massa tumorale che rimane risulta caratterizzata da cellule che smettono di crescere e proliferare e differenziano. Questo fenomeno è stato definito malattia minima residua (MRD). Il nostro scopo è quello di coltivare le xenosfere in vitro in 3D, embedded o sopra una matrice (Matrigel o Pura Matrix), e successivamente trattarle con terapie anti-EGFR per simulare l'effetto della malattia minima residua. Vogliamo inoltre capire quali sono i meccanismi molecolari coinvolti nel differenziamento, con l'obiettivo di individuare un possibile trattamento in grado di eliminare del tutto la MRD. Abbiamo dimostrato che la presenza del Matrigel, attorno alle xenosfere, è in grado di indurre un forte differenziamento. In particolare, è l'interazione tra l'integrina α6 e la laminina che media la polarizzazione delle cellule. Trattando poi le xenosfere RASWT, coltivate in Pura Matrix, con CTX o afatinib (inibitore dell'attività chinasica dell'EGFR), abbiamo osservato una notevole riduzione delle loro dimensioni e differenziamento. Possiamo quindi concludere che: (i) la cultura tridimensionale di linee di CRC è un ottimo modello per ricreare il fenotipo del tumore originario; (ii) la presenza della matrice è utile per ricreare l'ambiente circostante con cui il tumore interagisce in vivo, quindi le interazioni tra le proteine di membrana delle cellule e la matrice extracellulare; (iii) la terapia anti-EGFR è in grado di riprodurre gli effetti della MRD. Grazie a questo approccio, pratico e veloce, di cultura 3D in vitro, potremmo studiare i meccanismi di resistenza alle terapie, con lo scopo di individuare possibili strategie in grado di eliminare completamente il fenomeno della malattia minima residua.
4) Studio del ruolo di MRCKα nell'estrusione di cellule epiteliali
Abbiamo dimostrato che MRCKα è necessario per l'assemblaggio di un anello di actina apicale durante il processo di estrusione delle cellule epiteliali e che la sua attivazione dipende dal taglio della caspasi 3 in sequenze specifiche da noi individuate.
Sci. Rep. 2015 May 15; 5:10206
Real-time monitoring of cell protrusion dynamics by impedance responses.
Armando Gagliardi P, Puliafito A, di Blasio L, Chianale F, Somale D, Seano G, Bussolino F, Primo L.
Tuesday 21 March 2017
My Progress Report: "PDK1 targeting in mutated KRAS metastatic colorectal cancer"
held in Candiolo Cancer Institute
Friday 11 September 2015
My Progress Report: "Is PDK1 a therapeutic target for cancer?"
held at Candiolo Cancer Institute
ANNO 2017
Poster entitled: "PDK1 targeting in KRAS mutated metastatic colorectal cancer"
at MBC - September 19th 2017 - D-day 2017
ANNO 2016
Poster entitled: "PDK1 targeting in KRAS mutated metastatic colorectal cancer"
at EMBO EMBL Symposium "Organoids: Modelling organ development and disease in 3D culture"
held in Heidelberg, Germany - October 13th 2016
ANNO 2014
Poster entitled: "3-Phosphoinositide-Dependent Kinase 1 is required for anchorage independent growth of KRAS mutated cells"
at "Dangerous Liaisons: translating cancer biology into better patients management - 56° Congresso Nazionale Società Italiana di Cancerologia"
held in Ferrara, September 12th 2014
ANNO 2017
EACR-AACR-SIC Special conference on the challenges of optimising immuno and targeted therapies from cancer biology to the clinic.
held in Florence, Italy - June 24th-27th 2017
(utilizzando il budget: quota 10% della borsa di dottorato)
ANNO 2016
EMBO EMBL Symposium "Organoids: Modelling organ development and disease in 3D culture"
held in Heidelberg, Germany - October 12th-15th 2016
(utilizzando il budget: quota 10% della borsa di dottorato)
ANNO 2015
1) "Frontiers in Regenerative Medicine"
held at the Molecular Biotechnology Center (MBC), February 18th-20th 2015
2) The 2015 International Conference on Molecular Oncology "From Signal Transduction to Cancer Precision Medicine"
held at Candiolo Cancer Institute, June 6th-7th 2015
3) Beatson International Cancer Conference "Control of cell polarity and movement in cancer"
held at the Cancer Research UK Beatson Institute, Glasgow, Scotland. July 5th-8th 2105
(utilizzando il budget: quota 10% della borsa di dottorato)
ANNO 2014
1) Dangerous Liaisons: translating cancer biology into better patients management - 56° Congresso Nazionale Società Italiana di Cancerologia
held in Ferrara, September 11th-13th 2014
2) Conference "Molecular Clinical Oncology - Precision Medicine"
held at Candiolo Cancer Institute (TO), October 4th-5th 2014
ANNO 2017
held in Candiolo Cancer Institute:
1) PDX-derived cell line models for pharmacogenomics studies in colorectal cancer
Tuesday 20 December 2016, Luca Lazzari
2) Hijacking acquired resistance to anti-EGFR therapy in colorectal cancer
Tuesday 24 January 2017, Sabrina Arena
3) Next generation Liquid Biopsies: genotyping cancer in blood and other body fluids
Tuesday 21 February 2017, Giulia Siravegna
4) Role of the postsynaptic adhesion molecule NLGN1 in cancer
Tuesday 28 February 2017, Margherita Pergolizzi
5) Targeting the Met oncogene by concomitant inhibition of ligand and receptor by an antibody-decoy strategy
Tuesday 7 March 2017, Chiara Modica
6) Targeting BRAF in colorectal cancer
Tuesday 28 March 2017, Daniele Oddo
7) Loss of Neuroligin-2 promotes pancreatic ductal adenocarcinoma onset and progression by altering apical-basal polarity
Tuesday 2 May 2017, Emanuele Middonti
8) Genomic evolution in colorectal cancer cells
Tuesday 16 May 2017, Nabil Amirouchene Angelozzi
9) Precision medicine in colorectal cancer
Tuesday 23 May 2017, Silvia Marsoni
10) Metabolic reprogramming as a driver of stemness and tumorigenesis in the intestine.
Tuesday 30 May 2017, Carlos Sebastian
11) A pre-surgery protocol to investigate miR-100 as a predictor of response to hormonal therapy in breast cancer patients
Tuesday 6 June 2017, Annalisa Petrelli
12) L1-MET alternative transcript in breast cancer
Tuesday 11 July 2017, Umberto Miglio
13) Synergistic effect of BRAF and VEGF targeting in a BRAFV600E melanoma murine model
Tuesday 20 June 2017, Valentina Comunanza
14) Metabolic vulnerability of KRAS-mutant colorectal cancer
Tuesday 5 September 2017, Alessia Mira
15) Systematic screening for therapeutic targets in clinically aggressive colorectal cancer
Tuesday 12 September 2017, Federica Invrea
16) Charting features and vulnerabilities of residual colorectal tumors surviving EGFR blockade
Tuesday 26 September 2017, Barbara Lupo
17) TFEB inhibits fibroblast differentiation and activation program
Tuesday 3 October 2017, Elena Astanina
18) Reliance upon ancestral mutations is maintained in colorectal cancers that heterogeneously evolve during targeted therapies
Tuesday 10 October 2017, Mariangela Russo
19) A Sema3A mutant is an effective vascular normalizing and anti-cancer drug
Tuesday 24 October 2017, Federica Maione
20) Role of Neuroligin 1 and 2 in tumor-nervous-connections: approaches and issues
Tuesday 31 October 2017, Davide Pascal
21) Cell population dynamics in a xenospheres colon cancer model
Tuesday 7 November 2017, Alberto Puliafito
22) Neuropilin-1 controls cancer cell adaptation to target therapies
Tuesday 14 November 2017, Sabrina Rizzolio
23) Role of the transcription factor EB (TFEB) in angiogenesis and tumor progression
Tuesday 5 December 2017, Gabriella Doronzo
ANNO 2016
held at Candiolo Cancer Institute:
1) Regulation of Colorectal Cancer Stem Cells by Cytokine Networks: implications in self-renewal and resistance to therapies
Tuesday 24 November 2015, Viola Bigatto
2) Role of alpha6 integrin in pericytes dynamics and tumor vessels normalization
Tuesday 1 December 2015, Giulia Chiaverina
3) Semaphorin 6A and responsiveness to anti-EGFR targeted therapies in colorectal cancer
Tuesday 15 December 2015, Chiara Battistini
4) Semaphorin 6A and responsiveness to anti-EGFR targeted therapies in colorectal cancer
Tuesday 15 December 2015, Chiara Battistini
5) Strategies to improve half-life and potency of a Met therapeutic antibody
Tuesday 22 December 2015, Simona Cignetto
6) Collective directional migration in epithelial 3d models.
Tuesday 12 January 2016, Alberto Puliafito
7) High-throughput screening to unravel the influence of protein phosphatases on VEGF-A signaling
Tuesday 19 January 2016, Maria Alvaro
8) Role of the endoplasmic reticulum in the control of neuropilin 1 traffic and endothelial cell adhesion
Tuesday 2 February 2016, Giulia Villari
9) Intercepting acquired resistance to targeted therapies: how and when?
Tuesday 9 February 2016, Mariangela Russo
10) Caspase-mediated cleavage of MRCKα determines actin-myosin contraction and epithelial cell extrusion
Tuesday 1 March 2016, Paolo Gagliardi
11) Preclinical activity of Cytokine Induced Killer Cells (CIK) against sarcomas.
Tuesday 8 March 2016, Giulia Mesiano
12) RNA-based identification of actionable oncogenic drivers in colorectal cancer
Tuesday 15 March 2016, Sara Bellomo
13) Tfeb inhibits differentiation of coronary smooth muscle cells and fibroblasts by upregulation of TGF-β; and Notch pathways repressors
Tuesday 29 March 2016, Elena Astanina
14) TFEB governs a transcriptional program essential for angiogenic activities of VEGFR2
Tuesday 5 April 2016, Gabriella Doronzo
15) Xenospheres: a comprehensive patient-derived in vitro model to study response and resistance to targeted therapies in mCRC
Tuesday 26 April 2016, Paolo Luraghi
16) PPFIA1 drives active α5β1 integrin recycling from the TGN to control fibronectin fibrillogenesis and vascular morphogenesis
Tuesday 3 May 2016, Donatella Valdembri
17) Ras and Rab interacting protein 2 (RIN2) controls cell adhesion dynamics and signaling: implications for cancer angiogenesis and invasion
Tuesday 10 May 2016, Chiara Sandri
18) Generation of a platform of gastro-esophageal PDXs to identify and validate molecular targets
Tuesday 17 May 2016, Prof. Silvia Giordano
19) AGNOSTOS Project: a platform to unveil the mysteries of cancer of unknown primary (CUPS)
Tuesday 24 May 2016, Silvia Benvenuti
20) A potential strategy to counteract minimal residual disease in colorectal cancer after EGFR blockade.
Tuesday 31 May 2016, Barbara Lupo
21) Exploring glioblastoma heterogeneity at cancer stem cell level
Tuesday 7 June 2016, Francesca De Bacco
22) Precision oncology between challenges and opportunities: The example of colorectal cancer
Friday 10 June 2016, Prof. Livio Trusolino
23) The GEA platform as a tool to model gastric cancer therapy: focus on HER2
Tuesday 21 June 2016, Cristina Migliore
24) Cancer evolution as a therapeutic opportunity
Tuesday 28 June 2016, Prof. Alberto Bardelli
25) Patient-derived tumor xenograft model to study intratumour heterogeneity of epithelial ovarian carcinomas
Friday 15 July 2016, Prof. Maria Flavia Di Renzo
26) Proteomic survey reveals novel neuropilin-1 partners and functions in vascular endothelial cells
Tuesday 13 September 2016, Noemi Gioelli
27) Targeting Semaphorin 4A-expressing myeloid cells to impair cervical cancer progression
Tuesday 20 September 2016, Yaqi Qiu
28) Targeting anti-apoptotic reprogramming to counteract drug tolerance in EGFR-inhibited colorectal tumors
Tuesday 27 September 2016, Simonetta Leto
29) Novel functions of PlexinD1 signaling: nuclear localization and transcriptional regulation
Tuesday 4 October 2016, Gabriella Cagnoni
30) RN-tre/USP6NL in breast cancer cell fitness
Tuesday 11 October 2016, Daniele Avanzato
31) Reviving 'oncogenic addiction' to MET bypassed by BRAF (G469A) mutation.
Thursday 3 November 2016, Anna Rita Virzi
32) Inactivation of DNA repair triggers dynamic neoantigen evolution and impairs cancer growth
Tuesday 8 November 2016, Giovanni Germano
33) Enabling permanent in vivo transduction of patient-derived xenografts
Tuesday 15 November 2016, Consalvo Petti
34) "Manipulating the Neuregulin1/ErbB system in peripheral nerves: an in vitro and in vivo laboratory investigation." Davide Pascal, Department of Clinical and Biological Sciences, Orbassano (Torino) - a post doctoral applicant in Marco Arese laboratory (IRCCS)
ANNO 2015
held at Candiolo Cancer Institute:
1) Effects of MET trafficking on cancer cells growth
Tuesday 27 January 2015, Emanuela Pupo
2) Does chemotherapy affect the response to anti-EGFR therapy in colorectal cancer?
Tuesday 10 March 2015, Luca Lazzari
3) Neuroligin 2: a synaptic protein modulates the release of the angiogenic factor Angiopoietin 2
Tuesday 17 March 2015, Elena Riccitelli
4) Somatic mutations and human diseases: the paradigm of PIK3CA mutations in cancer, CLOVES syndrome and vascular malformations
Tuesday 24 March 2015, Laura Di Blasio
5) Characterizing the cross-talk between integrin mechanics and endocytosis
Tuesday 31 March 2015, Giulia Mana
6) Neuroligins in nerve-tumor interactions
Tuesday 26 May 2015, Laura Bizzozero
7) Genomics at the IRCC: the next generation
Tuesday 9 June 2015, The Bioinformatics Center (BIC)
8) Resistance to MET inhibitors: which is the role of tumor microenvironment?
Tuesday 16 June 2015, Maria Apicella
9) Tuesday 23 June 2015, Margherita Pergolizzi
10) RN-tre in breast cancer
Tuesday 15 September 2015, Nadia Ducano
11) Role of the synaptic protein Neuroligin-2 in the onset and progression of Pancreatic Ductal Adenocarcinoma
Tuesday 29 September 2015, Emanuele Middonti
12) Evaluation of trabectedin and olaparib activity in preclinical models of bone and soft tissue sarcomas
Tuesday 20 October 2015, Ymera Pignochino
13) Latrophilin 2/ADGRL2 controls class 3 semaphorin-to-Rap1 signaling and vascular morphogenesis
Tuesday 10 November 2015, Chiara Camillo
14) VEGF removal enhances the antitumor effect of BRAF inhibition by reprogramming the circuits between cancer and stroma
Tuesday 17 November 2015, Valentina Comunanza
PhD thesis:
held at Candiolo Cancer Institute:
1) Monday January 26th 2015, Dr. Valentina Martin: "Increase of MET gene copy number confers resistance to a monovalent MET antibody and establishes drug dependance"
2) Monday January 26th 2015, Dr. Erica Torchiaro: "RSK1 and RSK2 regulate motility and invasiveness of ovarian cancer cells"
held at the Molecular Biotechnology Center (MBC):
1) Friday Febraury 06th 2015, Dr. Chiara Camillo
2) Friday Febraury 06th 2015, Dr. Nadia Ducano
3) Friday Febraury 06th 2015, Dr. Gioelli Noemi
ANNO 2014
held at Candiolo Cancer Institute:
1) Tracking the Evolution of Drug Resistance by Genomic Barcoding.
Tuesday 11 November 2014, Beth Van Emburgh
2) Stromal contribution to the colorectal cancer transcriptome
Tuesday 4 November 2014, Claudio Isella
3) Killing circulating metastasis-initiating cells by MET-targeted Antibody-Dependent Cell-mediated Cytotoxicity
Tuesday 28 October 2014, Virginia Morello
4) A translational approach for mCRC: updates on the "xenopatient-xenosphere-spheropatient" platform and results on RASwt xenospheres.
Tuesday 14 October 2014, Paolo Luraghi
5) Real-time study of cell protrusion dynamics in response to growth factors: implications for cell migration and invasion
Tuesday 7 October 2014, Paolo Gagliardi
6) A pre-surgery protocol to define miR-100 as a predictor of response
to hormonal therapy in breast cancer
Tuesday 16 September 2014, Annalisa Petrelli
7) Notch signaling regulates PlexinD1 expression
Tuesday 9 September 2014, Michael Rehman
8) Preclinical identification and validation of the NEDD8 pathway inhibitor Pevonedistat as an effective treatment for colorectal cancer
Tuesday 8 July 2014, Gabriele Picco
9) Tfeb inhibits premature differentiation and migration of smooth muscle
cells progenitors during coronary vessel development.
Tuesday 1 July 2014, Elena Astanina
10) Analysis of hepatocellular carcinoma progression
Tuesday 27 May 2014, Silvia Menegon
11) Outlier kinase expression identifies new therapeutic targets for colorectal cancer
Tuesday 13 May 2014, Mariangela Russo
12) Semaphorin and responsiveness to anti-EGFR targeted therapies in CRC
Tuesday 6 May 2014, Chiara Battistini
13) Molecular characterization of RIN2, a key player of the Sema3/Plexin/R-Ras pathway in endothelial cells
Wednesday 23 April 2014, Chiara Sandri
14) The transcription factor EB (TFEB): role in angiogenesis
Tuesday 15 April 2014, Gabriella Doronzo
15) The dynamical response of EGFR from receptor activation to cell protrusions.
(Insights from modeling and experiments)
Tuesday 8 April 2014, Alberto Puliafito
16) High-throughput screening to unravel the influence of protein phosphatases on vegf-a signaling
Tuesday 25 March 2014, Maria Alvaro
17) RAF suppression improves the efficacy of MEK inhibitors in KRAS mutant colorectal cancer cells
Tuesday 18 March 2014, Simona Lamba
18) TNF-alpha promotes invasive growth through the MET signaling pathway
Tuesday 11 March 2014, Viola Bigatto
19) Characterizing the molecular mechanisms by which endothelial cells respond to class 3 semaphorins.
Monday 3 March 2014, Chiara Camillo
20) The role of alpha6 Integrin in sprouting angiogenesis
Tuesday 25 February 2014, Giulia Chiaverina
21) Development of 3D organoid culture to study the tumor-microenviroment interaction
Tuesday 18 February 2014, Valentina Comunanza
22) HGF confers resistance to anti-angiogenic drugs by protecting colorectal cancer cells against metabolic stress
Tuesday 11 February 2014, Alessia Mira
23) Zoledronic Acid improves anti-angiogenic therapy and chemotherapy by targeting M2-polarized Tumor-Associated Macrophages in a transgenic mouse model of cervical cancer
Tuesday 4 February 2014, Stefania Capano
24) Mechanisms of acquired resistance to anti-EGFR targeted therapies in metastatic colorectal cancer
Tuesday 21 January 2014, Sandra Misale
25) The GTPase-Activating Protein RN-tre Controls Focal Adhesion Turnover and Cell Migration
Tuesday 14 January 2014, Nadia Ducano
26) Tracking the Evolution of Drug Resistance by Genomic Barcoding.
Tuesday 11 November 2014, Beth Van Emburgh
27) Regulation of sprouting angiogenesis by transcriptional and post-transcriptional network motifs
Tuesday 18 November 2014, Stefania Rosano
28) Activation of RAS family members confers resistance to ROS1 targeting drugs
Tuesday 25 November 2014, Marilisa Cargnelutti
ANNO 2017
1) "Clinical Translation of the Cancer Genome" by Prof. Elaine Mardis, Washington University School of Medicine, St. Louis (U.S.A.) - at IRCC - 14 December 2016
2) AIRC Special Program "Molecular Clinical Oncology" Advisory Board Audit
at IRCC - 12/13 January 2017
3) "Intratumor heterogeneity in brain cancer" by Prof. Joan Seoane, Ph.D. - ICREA Research, Vall d'Hebron Institute of Oncology (VHIO), Universitat Autònoma de Barcelona, Barcelona, Spain
at IRCC - 19 January 2017
4) "Liquid biopsy: Potential and challenges of circulating tumor cell research" by Prof. Klaus Pantel, M.D. - University Medical Center, Institute of Tumor Biology, Hamburg (Germany)
at IRCC - 19 January 2017
5) "Understanding the role of BRCA2 tumour suppressor protein in DNA metabolism" by Prof. Vincenzo Costanzo
at IRCC - 28 February 2017
6) "An integrated ATR, ATM and mTOR-mechanical network controlling nuclear plasticity and cell migration" by Prof. Marco Foiani
at IRCC - 3 March 2017
7) Giornata Studio Guido Tarone
at MBC - 22 May 2017
8) "Animal models as useful tools for the study of hepatocarcinogenesis?" by Prof. Amedeo Columbano, University of Cagliari, Italy
at MBC - 19 September 2017
9) "Advanced genetic engineering to broaden gene therapy application to the treatment of inherited diseases and cancer?" by Prof. Luigi Naldini, "Vita-Salute" San Raffaele University, Milano, Italy
at MBC - 19 September 2017
10) "Pro-invasive tumour-stroma interactions: role of cancer associated fibroblasts" by Sara Zanivan - Tumour Microenvironment and Proteomics Lab, CRUK Beatson Institute, Glasgow University
at IRCC - 10 November 2017
ANNO 2016
1) "Regulation of self renewal in Cancer Stem Cells" by Prof. Pier Giuseppe Pelicci
held in the IRCCS, Friday 11 December 2015
2) "The impact of human retrotransposons on cancer" by Dr. Szilvia Solyom held in the IRCCS, 26 January 2016
3) "The transparent editorial process, data reproducibility and research integrity at EMBO"
by Roberto Buccione held in the IRCCS, Tuesday 22 March 2016
4) "Breast Cancer stem Cells targeting: a new step for intratumoral heterogeneity in the light of personalized medicine" by Prof. Emmanuelle Charafe Jauffret, Aix-Marseille Université, CRCM, Institut Paoli-Calmettes, CNRS, Marseille - held in the IRCCS, Friday 25 March 2016
5) "AIRC Support to Cancer Research: Strategies and Perspectives" by Prof. Federico Caligaris-Cappio, Scientific Director, Italian Association for Cancer Research, Milano - held in the IRCCS, Friday 29 April 2016
6) "Control of cell identity by polycomb group proteins " by Prof. Davide Pasini, Director of the Epigenetic mechanisms in stem cell differentiation and oncogenesis Unit, IEO Milano - held in IRCCS, Friday 27 May 2016
7) "Visualizing spatio-temporal signaling networks regulating cell fate and morphogenesis" by Prof. Olivier Pertz, Cellular Dynamics Lab, Institute of Cell Biology, University of Bern (Switzerland) - held in the IRCCS, Friday 17 June 2016
8) D-Day, held at the MBC, 15 September 2016
9) "Neutral evolution in cancer: distinguishing functional from nonfunctional intra-tumour heterogeneity" by Dr Andrea Sottoriva of the The Institute of Cancer Research, London, UK - on Monday, September 19th
10) "Mechanisms regulating tumor heterogeneity" by Prof. Cedric Blanpain, IRIBHM, Université Libre de Bruxelles (ULB). Held in IRCCS. Friday 21 October 2016
ANNO 2015
1) Dr Normanno "Tumor heterogeneity in colon cancer: therapeutic implications"
held at Candiolo Cancer Institute, Monday January 26th
2) "Il trasferimento di conoscenze in Ateneo: dalla ricerca alla valorizzazione dell'innovazione"
at the Campus Luigi Einaudi, February 3th 2015. Seminar organized by "Scuole di Dottorato" in collaboration with "Sezione Brevetti e trasferimento di Conoscenze"
3) "Neuropilin and Integrin Control of Cancer Stem Cell Fate"
by Arthur Mercurio, University of Massachussetts Medical School, USA
held at Candiolo Cancer Institute, Friday 20 March 2015
4) D-day 2015 della Scuola di Dottorato in Scienze della Vita e della Salute
held in "Aula Magna" at Rettorato dell'Università di Torino, September 16th 2015
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