Body

Prostate cancer screening could be over-accurate

The introduction of prostate-antigen screening, or PSA, has resulted in over 1 million additional men over the last 23 years being diagnosed and treated for prostate cancer —— most of whom were likely overdiagnosed, researchers reported in a new study published in the Journal of the National Cancer Institute.

Overdiagnosis has been associated with early diagnosis in prostate cancer, but there have been no previous national estimates of its magnitude.

'Watchful waiting' is a viable option for prostate cancer patients with low-risk tumors

Prostate cancer patients, including older men and men with small, low-risk tumors, may safely defer treatment for many years with no adverse consequences, according to a new study in the Journal of Clinical Oncology (JCO). Led by researchers at Beth Israel Deaconess Medical Center (BIDMC), the study appears online today.

Mastectomy decisions among racially and ethnically diverse breast cancer patients

Women diagnosed with nonmetastatic breast cancer who were concerned about body image and their spouse's opinion were less likely to have a mastectomy than those who placed less concern on these issues, according to new study published online August 31 in the Journal of the National Cancer Institute. Overall, patients who were more involved in the decision making about their treatment were more likely to have a mastectomy, regardless of racial or ethnic group.

Protein-telomere interactions could be key in treating cancer and aging

A team of researchers from The Wistar Institute have shown that a large non-coding RNA in mammals and yeast plays a central role in helping maintain telomeres, the tips of chromosomes that contain important genetic information and help regulate cell division. Since this RNA also facilitates the formation of DNA at telomeres —— a process that can protect aging cells and destabilize tumor cells —— manipulating its expression may be useful in treating cancer and other diseases.

Mutations in the PYCR1 gene are responsible for wrinkly skin syndrome

Scientists in Singapore and Germany report that mutations in the PYCR1 gene cause the rare genetic condition that results in premature skin aging and that is known as "wrinkly skin syndrome," and report this in Nature Genetics.

Their findings not only suggest that increasing levels of the PYCR1 protein could reverse conditions that cause fast aging and wrinkly skin but also provide insight into how some unexpected genes help maintain youthful skin.

Researchers find gene tied to melanoma

Drawing on the power of DNA sequencing, National Institutes of Health researchers have identified a new group of genetic mutations involved in the deadliest form of skin cancer, melanoma. This discovery is particularly encouraging because some of the mutations, which were found in nearly one-fifth of melanoma cases, reside in a gene already targeted by a drug approved for certain types of breast cancer.

Combination of natural diet and chemotherapy is new recipe for cancer treatment

Research in the Linus Pauling Institute at Oregon State University suggests that some natural food compounds, which previously have been studied for their ability to prevent cancer, may be able to play a more significant role in treating it – working side-by-side with the conventional drugs that are now used in chemotherapy.

Women, blacks, Medicare recipients less likely to be evaluated for liver transplantation

PITTSBURGH, Aug. 31 – Patient race, gender and insurance status influence decisions about who will go on to receive liver transplants, according to a University of Pittsburgh School of Medicine study. Available online and published in the September issue of the American Journal of Transplantation, the study indicates that women, blacks and patients with Medicare who are in end-stage liver disease are less likely to be referred and evaluated for liver transplantation.

New family care model aids at-risk families

Columbus, Ohio—August 31, 2009— Many families struggle on a day-to-day basis with insufficient in-home care or problematic out-of-home care for their emotionally or behaviorally troubled children and adolescents. Researchers have recently shown that an integrative family care model, which incorporates the strengths of external agencies and care providers, may be the answer. The latest issue of Family Process features this new model.

Genes in prevention: Hopes and doubts

Barcelona, Spain, 30 August: At present almost every month there are papers reporting the discovery of new genetic variants that affect the risk of coronary artery disease and heart attacks. This is a truly exciting time for both researchers and clinicians interested in understanding the genetic basis of heart disease. The findings will undoubtedly lead to new biological insights into the mechanisms that cause heart attacks which in turn may result in the future new types of treatments. Will this new genetic information be useful in preventing heart attacks and if so how?

Finding the ZIP-code for gene therapy: Scientists imitate viruses to deliver therapeutic genes

A research report featured on the cover of the September 2009 print issue of The FASEB Journal (http://www.fasebj.org) describes how Australian scientists developed a new gene therapy vector that uses the same machinery that viruses use to transport their cargo into our cells. As a result of this achievement, therapeutic DNA can be transferred to a cell's nucleus far more efficiently than in the past, raising hopes for more effective treatment of genetic disorders and some types of cancers.

The huge opportunities for transcatheter aortic valve implantation

Barcelona, Spain, 30 August: "Today, transcatheter aortic valve implantation (TAVI) represents an effective therapeutic alternative to conventional aortic valve replacement for patients who are at high risk or with contraindications to surgery, and the combination of the transfemoral and transapical approaches further increases the number of patients who can be treated" said Prof Dominique HIMBERT from the Bichat Hospital in Paris France, at a press conference at the ESC Congress in Barcelona.

Heart failure: More or less malignant than cancer?

Barcelona, Spain, 30 August: A recently completed analysis of over one million hospital cases in Sweden during the period 1988 to 2004 has revealed that heart failure, relative to most common forms of cancer specific to men and women, represents a major health burden in respect to the risk of being hospitalised for the first time, poor overall survival and the number of premature life-years lost.

Ongoing challenges for cardiovascular prevention in Europe

Barcelona, Spain, 31 August: A comprehensive strategy, focusing on changes in lifestyle and on the management of risk factors, is needed to prevent premature mortality and reduction of life expectancy in good health due to cardiovascular disease (CVD). The European Heart Health Charter has established a roadmap for European countries.

New European guidelines on pulmonary hypertension provide new 6-group clinical definition

Barcelona, Spain, 31 August: New 2009 Guidelines for the diagnosis and treatment of pulmonary hypertension are made public today. The Guidelines have been jointly produced by a Task Force of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS); the Task Force also included experts from the International Society of Heart and Lung Transplantation (ISHLT).