PROSPER

Prostate cancer: profiling and evaluation of ncRNA

 Coordinatore TAMPEREEN YLIOPISTO 

 Organization address address: Kalevantie 4
city: TAMPERE
postcode: 33014

contact info
Titolo: Ms.
Nome: Hannele
Cognome: Auffermann
Email: send email
Telefono: +358 40 5441845
Fax: +358 3 35518970

 Nazionalità Coordinatore Finland [FI]
 Sito del progetto http://www.uta.fi/imt/ProspeR/
 Totale costo 3˙971˙688 €
 EC contributo 2˙986˙216 €
 Programma FP7-HEALTH
Specific Programme "Cooperation": Health
 Code Call FP7-HEALTH-2007-A
 Funding Scheme CP-FP
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-02-01   -   2012-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TAMPEREEN YLIOPISTO

 Organization address address: Kalevantie 4
city: TAMPERE
postcode: 33014

contact info
Titolo: Ms.
Nome: Hannele
Cognome: Auffermann
Email: send email
Telefono: +358 40 5441845
Fax: +358 3 35518970

FI (TAMPERE) coordinator 0.00
2    ERASMUS UNIVERSITAIR MEDISCH CENTRUM ROTTERDAM

 Organization address address: 's Gravendijkwal 230
city: ROTTERDAM
postcode: 3015CE

contact info
Titolo: Ms.
Nome: Nuran
Cognome: Tuzen
Email: send email
Telefono: +31 10 7043211
Fax: 31107044743

NL (ROTTERDAM) participant 0.00
3    EXIQON A/S

 Organization address address: Bygstubben 9
city: VEDBAEK
postcode: 2950

contact info
Titolo: Dr.
Nome: Søren
Cognome: Echwald
Email: send email
Telefono: +45 4565 0454
Fax: +45 4566 1888

DK (VEDBAEK) participant 0.00
4    LUNDS UNIVERSITET

 Organization address address: Paradisgatan 5c
city: LUND
postcode: 22100

contact info
Titolo: Prof.
Nome: Kristian
Cognome: Riesbeck
Email: send email
Telefono: +46 40 338494
Fax: +46 40 391177

SE (LUND) participant 0.00
5    ORION CORPORATION

 Organization address address: ORIONINTIE 1
city: ESPOO
postcode: 2200

contact info
Titolo: Mr.
Nome: Ville
Cognome: Hassinen
Email: send email
Telefono: +358 10 426 4755
Fax: +358 10 426 4682

FI (ESPOO) participant 0.00
6    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Linda
Cognome: Polik
Email: send email
Telefono: +44 1865 289811
Fax: +44 1865 289801

UK (OXFORD) participant 0.00
7    THE UNIVERSITY OF SHEFFIELD

 Organization address address: FIRTH COURT WESTERN BANK
city: SHEFFIELD
postcode: S10 2TN

contact info
Titolo: Ms.
Nome: Joanne
Cognome: Watson
Email: send email
Telefono: +44 114 2224754
Fax: +44 114 2221455

UK (SHEFFIELD) participant 0.00
8    TURUN YLIOPISTO

 Organization address address: YLIOPISTONMAKI
city: TURUN YLIOPISTO
postcode: 20014

contact info
Titolo: Dr.
Nome: Eliisa
Cognome: Särkilahti
Email: send email
Telefono: +358 2 3336155
Fax: +358 2 3336446

FI (TURUN YLIOPISTO) participant 0.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

cancer    ncrna    mirna    ncrnas    samples    function    drug    discovery    androgen    molecular    therapeutic    largely    signalling    prosper    androgens    tools    regulators    translational    expression    diagnosis    symptoms    rate    impact    antigen    prostate    prognostic    mirnas    cellular    clinical    lack    mechanisms    detection    unknown    scientists    diagnostic    progression    coding    apart    psa    receptor    treatment   

 Obiettivo del progetto (Objective)

'Annually, over 200 000 new prostate cancer cases are diagnosed in Europe. This number is expected to further increase due to widespread use of prostate specific antigen (PSA) tests on asymptomatic men and an aging population. This leads to high rate of over-detection, where most cases will never experience cancer symptoms during their lifetime. Hence, our current lack of means to predict prostate cancer prognosis will have devastating impact on both life-quality and health care expenditures. Molecular mechanisms of the development of prostate cancer are largely unknown apart from the recognized role of androgens. Lack of knowledge on mechanisms leading to the development and progression of this cancer hampers development of efficacious prevention, specific diagnostics, prognostic, and therapeutic tools. Based on the emerging knowledge on the function of non-coding RNAs (ncRNAs) as regulators of key cellular mechanisms and our own preliminary data on expression of ncRNAs in prostate cancer, it is very likely that ncRNAs are involved in the tumorigenesis and progression of prostate cancer. Our planned studies of ncRNAs can contribute major breakthroughs to optimize individualized prostate cancer treatment by providing both novel biomarkers and drug targets. In this project, we will pursue two major clinical problems: 1) early identification of cases requiring aggressive curative treatment, and 2) develop efficient therapies against hormone-refractory prostate cancer. The project will cover all phases of translational research, from discovery to validation and implementation. We will identify novel ncRNAs, investigate their expression, genetic/epigenetic alterations, and function. We will develop diagnostic tools, identify and validate therapeutic targets. To assure the success of the project, our consortium consists of leading translational prostate cancer research centers in Europe and companies committed to develop ncRNA detection technologies and novel drugs.'

Descrizione progetto (Article)

Diagnosis of prostate cancer is largely based on testing positive for the prostate-specific antigen (PSA). This is increases the rate of over-detection without necessarily correlating with cancer symptoms.

Apart from the role of androgens in the development of prostate cancer, the effect of molecular mechanisms such as non-coding ribonucleic acids (ncRNAs) is unknown. The EU-funded 'Prostate cancer: Profiling and evaluation of ncRNA' (PROSPER) project proposed to explore the role of ncRNAs (regulators of key cellular mechanisms) in prostate cancer. Project members will also evaluate the potential use of ncRNAs in diagnostic and prognostic tools as well as therapy targets.

As a first step, scientists performed global microRNA (miRNA) expression analysis in prostate cancer samples, which led to the discovery of 20 novel miRNAs. Microarray analyses of miRNAs in over 180 prostate cancer samples indicated that androgens and/or the androgen receptor were instrumental in regulating expression of some miRNAs. Androgen signalling models verified the impact of androgen signalling on miRNA expression and also located androgen receptor binding sites near some of these miRNAs.

For prognostic and diagnostic purposes, http://www.uta.fi/ibt/institute/research/visakorpi/prosper.html (PROSPER) scientists identified a panel of 25 and 56 miRNAs, respectively, to distinguish between normal and prostate cancer samples. miRNAs with oncogenic or tumour suppressor activity in prostate cancer were also identified.

The prognostic and diagnostic miRNA panels developed during PROSPER could significantly improve the clinical diagnosis of prostate cancer and reduce unnecessary patient treatment. They also opened up new avenues for drug design and therapeutic exploitation.

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