prostate cancer

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Repressão epigenética do miR-130a promove cancro da Próstata através da interação com os genes SEC23B e DEPDC1

O grupo de Epigenética & Biologia do Cancro do Centro de Investigação do IPO-Porto, em colaboração com investigadores do Departamento de Oncologia Molecular do Hospital Universitário de Oslo, Noruega, demonstraram recentemente a função supressora tumoral do microRNA-130a no cancro da próstata. O carcinoma da próstata (CaP) é uma das neoplasias malignas com maior incidência e prevalência no sexo masculino, constituindo uma das principais causas de morbilidade e mortalidade oncológica.

Prostate cancer prognosis defined by the combined analysis of 8q, PTEN and ERG

Prostate cancer (PCa) is the second most frequently diagnosed non-skin cancer in men worldwide and the fifth cause of cancer-related deaths. The introduction of serum prostate-specific antigen (PSA) analysis constituted an important clinical tool for early PCa detection and disease monitoring, but this test has modest sensitivity and specificity and has limited prognostic value. This shows that there is an unmet need of novel diagnostic and prognostic markers for PCa clinical management.

Hypermethylation of the TERT promoter predicts biochemical recurrence in prostate cancer: a retrospective study

Prostate cancer (PC) is the most common cancer in the male population with a high prevalence from 60 years old. Despite the high prevalence, mortality rates are variable and reflect the heterogeneous nature (clinical and biological) of this disease. Recent studies have shown that most patients with low-risk disease do not need treatment. However, in this apparently homogeneous group, there are patients who have aggressive disease - and benefit from therapy.

Brachyury as a potential modulator of androgen receptor activity and a key player in therapy resistance in prostate cancer

Authors and Affiliations:

Filipe Pinto1,2, Nelma Pértega-Gomes3, José R. Vizcaíno4, Raquel P. Andrade5,6, Flavio M. Cárcano7,8, Rui M. Reis1,2,8

1 Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal

2 ICVS/3B’s – PT Government Associate Laboratory, Braga/Guimarães, Portugal

3 Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts

NCOA2 is a candidate target gene of 8q gain associated with clinically aggressive prostate cancer

 

Prostate cancer (PCa) remains a major health burden in men, being the second most common non-skin cancer and the fifth leading cause of death from cancer worldwide. Despite the use of serum prostate-specific antigen (PSA) as an important clinical tool for early PCa detection, this test has many shortcomings and has limited prognostic value. Therefore, there is a need of more reliable diagnostic markers to complement PSA, as well as better prognostic markers to differentiate aggressive from indolent tumors.

Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients

Hereditary prostate cancer is estimated to account for 5-10% of all prostate cancer cases, but the identification of highly penetrant genes has been difficult. HOXB13 was recently identified as a susceptibility gene for prostate cancer (PrCa) when the rare, but recurrent, germline mutation [G84E, p.(Gly84Glu)] was found in men of European descent, conferring an increased PrCa risk of 4.51-fold.

Post-treated prostate cancer: normal findings and signs of local relapse on multiparametric magnetic resonance imaging

Authors and Affiliations:

Lopes Dias J1,2,3, Lucas R4, Magalhães Pina J5,6, João R5,6, Costa NV7,6, Leal C8,6, Bilhim T7,6, Campos Pinheiro L7,6, Mateus Marques R7,6.

1Department of Radiology, Hospital de S. José, Rua José António Serrano, 1150-199, Lisbon, Portugal

Regucalcin may prevent the development of prostate age-related pathologies by modulating oxidative stress, cell proliferation and apoptosis

Researchers from the Health Sciences Research Centre of the University of Beira Interior (CICS-UBI) previously established the role of Regucalcin (RGN) in the control of cell survival and proliferation in prostate, and demonstrated that RGN is a protein underexpressed in prostate cancer cases. Now these researchers evaluated the effect of RGN on aging, a well-known risk factor for the development of prostate cancer. Making use of knock-in animals for RGN, the impact of RGN overexpression in cell aging was determined in what concerns cell proliferation, apoptosis and oxidative stress.

Prostate cancer cell in the context of co-overexpression

Diana Mesquita1, João D. Barros-Silva1, Joana Santos1, Rolf I. Skotheim2,3, Ragnhild A. Lothe2,3, Paula Paulo1,2,3 and Manuel R. Teixeira1,3,4

1 Department of Genetics and Cancer Genetics Group – CI-IPOP, Portuguese Oncology Institute, Porto, Portugal

Prostate cancer: signs of local relapse on multiparametric magnetic resonance imaging

Authors and Affiliations:

João Lopes Dias, MD (1), Rita Lucas, MD (2), João Magalhães Pina, MD (3), Raquel João, MD (3), Nuno Vasco Costa, MD (1), Cecília Leal, MD (4), Tiago Bilhim, MD, PhD (1), Luís Campos Pinheiro, MD, PhD (1), Rui Mateus Marques, MD, PhD (1)

(1) Department of Radiology, Hospital de S. José, Lisboa, Portugal

(2) Department of Radiology, Hospital de Santo António dos Capuchos, Lisboa, Portugal

(3) Department of Urology, Hospital de S. José, Lisboa, Portugal