Tag Archives: genetics

Proteins that deliver leucine to prostate cancer cells are therapeutic targets

To investigate the function of LATs in prostate cancer, Qian Wang, Ph.D., of the Origins of Cancer Laboratory, Centenary Institute, Sydney, Australia, and colleagues studied LAT3 expression in tissue samples from prostate cancer patients, analyzed the function of LATs in cancer cells in vitro, used microarray data to determine which genes and pathways are associated with LAT function, and assessed the role of LAT1 and LAT3 in tumor formation, growth, and metastasis in mice. The researchers found that LAT3 was expressed at all stages of prostate cancer and that inhibition of LAT proteins inhibits nutrient signaling pathways and over 100 metastasis-related genes, including E2F transcription factors, resulting in cell cycle inhibition. In mice injected with prostate cancer cells, tumor formation, metastasis, and cell cycle progression were all inhibited when the LAT1 or LAT3 gene was knocked out. The authors conclude that "Targeting LAT transporters, thereby inhibiting leucine uptake, may offer a new therapeutic opportunity for metastatic CRPC, affecting tumor growth and metastasis through inhibition of M-phase cell cycle and mTORC1 signaling pathways." Wang et al…

Genetic cause of childhood leukemia identified

"We’re in uncharted territory," said study author Kenneth Offit, MD, MPH, Chief of the Clinical Genetics Service at Memorial Sloan-Kettering. "At the very least this discovery gives us a new window into inherited causes of childhood leukemia. More immediately, testing for this mutation may allow affected families to prevent leukemia in future generations." The mutation was first observed in a family treated at Memorial Sloan-Kettering of which several family members of different generations had been diagnosed with childhood acute lymphoblastic leukemia (ALL). A second, non-related, leukemia-prone family cared for at a different hospital was later found to have the same mutation…

Gene variations may help predict cancer treatment response

The researchers analyzed DNA sequence variations in 651 non-small cell lung cancer patients, paying close attention to 53 inflammation-related genes. They found that four of the top 15 variants associated with survival were located on one specific gene (TNFRSF10B). In the study, these variants increased the risk of death as much as 41 percent. …

Genes that drive brain cancer revealed

The study was published August 5, 2013, in Nature Genetics. "Cancers rely on driver genes to remain cancers, and driver genes are the best targets for therapy," said Antonio Iavarone, MD, professor of pathology and neurology at Columbia University Medical Center and a principal author of the study. "Once you know the driver in a particular tumor and you hit it, the cancer collapses. We think our study has identified the vast majority of drivers in glioblastoma, and therefore a list of the most important targets for glioblastoma drug development and the basis for personalized treatment of brain cancer." Personalized treatment could be a reality soon for about 15 percent of glioblastoma patients, said Anna Lasorella, MD, associate professor of pediatrics and of pathology & cell biology at CUMC. …

Chromosomal abnormalities may explain increased cancer risk in type 2 diabetes

Their work was published on July 14, 2013 on the Nature Genetics website. There are more than 200 million diabetics worldwide, and one in three suffer from vascular or nerve complications. In 2012, two studies published in Nature Genetics showed that large chromosomal clonal mosaic events (CMEs)(2) affecting large portions of chromosomes (or even their totality), could be observed in the DNA of blood or saliva cells from some ageing individuals. These studies also suggested that CMEs could predict the risk of cancer, and notably leukemia, in these individuals. …

Comprehensive list of gene variants developed for cancer cells from nine tissue types

The NCI-60 cancer cell panel represents nine different types of cancer: breast, ovary, prostate, colon, lung, kidney, brain, leukemia, and melanoma. In this study, the investigators sequenced the whole exomes, or DNA coding regions, of each of NCI-60 cell lines, to define novel cancer variants and aberrant patterns of gene expression in tumor cells and to relate such patterns and variants to those that occur during the development of cancer…