Lasers Penetrate Cancer's Gene SecretsJuly 04, 2002LIGHT SABRES and phaser guns may be the stuff of science fiction, but laser technology has brought an important step forward in our present-day understanding of cancer, a study reveals this week.* By using miniature lasers to probe pancreatic tumours, Cancer Research UK scientists have implicated three new genes in the development of the disease. Their discovery could be important for the treatment of pancreatic cancer, as scientists aim to develop new drugs targeted at the genes. And researchers are optimistic that using lasers will accelerate progress against a number of other cancers. Pancreatic cancer affects nearly 7,000 people in the UK each year and has a very poor survival rate. The disease has proved difficult to study, since pancreatic tumours are a complex mix of cancer cells and non-cancerous tissue. Analysing a tumour as a whole fails to give an accurate picture of what is going on within the cancer cells. But Prof Nick Lemoine and his colleagues at Cancer Research UK's Molecular Oncology Unit in Hammersmith used lasers to cut out slivers of 'pure cancer' from the heart of each tumour. The technique - called Laser Capture Microdissection - allowed them to analyse the cancer cells in unprecedented detail, measuring the genetic changes that occur during the development of the disease. Prof Lemoine comments: "Our knowledge of pancreatic cancer has been held back by the lack of the technology needed to separate out the cancer cells from all the surrounding mess. But by combining laser technology with conventional techniques, we've been able to home in on the disease's genetic causes much more closely than was possible before." Scientists are interested not only in which genes are turned on in cancer, but the level to which they are switched. Each gene is controlled by the equivalent of a volume control, and, scientists found that three genes - called ABL2, Notch4 and SOD1 - were turned up to a much higher volume in cancer cells than in their healthy counterparts. They believe these are likely to be crucial to cancer's growth and development and could be important targets for drugs of the future. Prof Lemoine adds: "We're really excited by our discovery, as these genes all appear to be extremely important in the development of pancreatic cancer. We're already in the process of finding out exactly what the genes do in cancer cells, and the next step will be to develop drugs to block their function." Sir Paul Nurse, Interim Chief Executive of Cancer Research UK, says: "Cancer is a highly complex disease and it often takes a fresh approach to move our understanding forward. Until now we had no idea that any of these genes were involved in the disease, so it's an important step forward in our search for new gene-targeted treatments." Ends | |||||||||||||||||||||
|
Related Pancreatic Cancer Current Events and Pancreatic Cancer News Articles Stanford blood scanner detects even faint indicators of cancer A team led by Stanford researchers has developed a prototype blood scanner that can find cancer markers in the bloodstream in early stages of the disease, potentially allowing for earlier treatment and dramatically improved chances of survival. 2 new compounds show promise for eliminating breast cancer tumors Two new compounds created by a University of Central Florida professor show early promise for destroying breast cancer tumors. The miseries of allergies just may help prevent some cancers, study finds There may be a silver -- and healthy -- lining to the miserable cloud of allergy symptoms: Sneezing, coughing, tearing and itching just may help prevent cancer -- particularly colon, skin, bladder, mouth, throat, uterus and cervix, lung and gastrointestinal tract cancer, according to a new Cornell study. Cancer drugs my build and not tear down blood vessels Scientists have thought that one way to foil a tumor from generating blood vessels to feed its growth - a process called angiogenesis - was by creating drugs aimed at stopping a key vessel growth-promoting protein. But now the opposite seems to be true. UC Davis researchers discover Achilles' heel in pancreatic cancer UC Davis Cancer Center researchers have discovered a metabolic deficiency in pancreatic cancer cells that can be used to slow the progress of the deadliest of all cancers. Jefferson Department of Surgery announces new pancreas tumor registry Charles J. Yeo, M.D., Samuel D. Gross Professor and Chair, Department of Surgery at Jefferson Medical College of Thomas Jefferson University, announces the establishment of the new Jefferson Pancreas Tumor Registry (JPTR). Supercomputer provides massive computational boost to biomedical research at TGen In less time than the blink of an eye, the Translational Genomics Research Institute's new supercomputer at Arizona State University can do operations equal to every dollar in the recent Wall Street bailout. Hepatitis B exposure may increase risk for pancreatic cancer In a first-of-its-kind finding, researchers at The University of Texas M. D. Anderson Cancer Center have discovered that exposure to the hepatitis B virus (HBV) may increase the risk of pancreatic cancer. Study finds association between hepatitis B and pancreatic cancer A new study has shown that evidence of past hepatitis B infection was twice as common in people with pancreatic cancer than in healthy controls. This study is the first to report an association between past exposure to the hepatitis B virus and pancreatic cancer, but researchers cautioned that more studies are necessary to evaluate the nature of the link. Jefferson scientists deliver toxic genes to effectively kill pancreatic cancer cells A research team, led by investigators at the Department of Surgery at Jefferson Medical College of Thomas Jefferson University and the Kimmel Cancer Center at Jefferson, has achieved a substantial "kill" of pancreatic cancer cells by using nanoparticles to successfully deliver a deadly diphtheria toxin gene. More Pancreatic Cancer Current Events and Pancreatic Cancer News Articles |
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||