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Wednesday, August 31, 2011

'Anti-cancer virus' shows promise'



An engineered virus, injected into the blood, can selectively target cancer cells throughout the body in what researchers have labelled a medical first.
The virus attacked only tumours, leaving the healthy tissue alone, in a small trial on 23 patients, according to the journal Nature.
SPL
Modified vaccinia virus can target cancer


Researchers said the findings could one day "truly transform" therapies.
Cancer specialists said using viruses showed "real promise".
Using viruses to attack cancers is not a new concept, but they have needed to be injected directly into tumours in order to evade the immune system.
Smallpox to cancer
Scientists modified the vaccinia virus, which is more famous for being used to develop a smallpox vaccine.
The virus, named JX-594, is dependent upon a chemical pathway, common in some cancers, in order to replicate.
It was injected at different doses into the blood of 23 patients with cancers which had spread to multiple organs in the body.

Start Quote

I believe that some day, viruses and other biological therapies could truly transform our approach for treating cancer”
Prof John BellUniversity of Ottawa
In the eight patients receiving the highest dose, seven had the virus replicating in their tumours, but not in healthy tissue.
Prof John Bell, lead researcher and from the University of Ottawa, said: "We are very excited because this is the first time in medical history that a viral therapy has been shown to consistently and selectively replicate in cancer tissue after intravenous infusion in humans.
"Intravenous delivery is crucial for cancer treatment because it allows us to target tumours throughout the body as opposed to just those that we can directly inject."
Infection prevented further tumour growth in six patients for a time. However, the virus did not cure cancer. Patients were given only one dose of the virus as the trial was designed to test the safety of the virus.
It is thought that the virus could be used to deliver treatments directly to cancerous cells in high concentrations.
Prof Bell acknowledges that the research is still in the very early stages, but he said: "I believe that some day, viruses and other biological therapies could truly transform our approach for treating cancer."
Cancer Research UK's Prof Nick Lemoine, also director of Barts Cancer Institute, said: "Viruses that multiply in just tumour cells - avoiding healthy cells - are showing real promise as a new biological approach to target hard-to-treat cancers.
"This new study is important because it shows that a virus previously used safely to vaccinate against smallpox in millions of people can now be modified to reach cancers through the bloodstream - even after cancer has spread widely through the patient's body.
"It is particularly encouraging that responses were seen even in tumours like mesothelioma, a cancer which can be particularly hard to treat."

Friday, August 19, 2011

Test Taking Strategies Video Series

        Test Taking Strategies (Video Series)

Test-Taking Strategies 1 (of 12): Eliminating Wrong Answers
http://youtu.be/l0P5U9s4wYE

Test-Taking Strategies 2 (of 12): Working Backwards
http://youtu.be/vEF_mkeFawU

Test-Taking Strategies 3 (of 12): Solving Easy Problems First
http://youtu.be/4XYMkBib9Cw

Test-Taking Strategies 4 (of 12): Staying Relaxed
http://youtu.be/bvQHk9WUjKg

Test-Taking Strategies 5 (of 12): The Secret Spill (Brain Dump)
http://youtu.be/f5YjVNgWjpU

Test-Taking Strategies 6 (of 12): Show Your Work (Use Your Pencil!)

Test-Taking Strategies 7 (of 12): Tricky Words (Game Changers)

Test-Taking Strategies 8 (of 12): "All" or "None" Answers

Test-Taking Strategies 9 (of 12): The Comfortable Pace
http://youtu.be/FnXQ5cepJXA

Test-Taking Strategies 11 (of 12): Estimate or Do the Minimum
http://youtu.be/fphJw_G2iZY

Test-Taking Strategies 12 (of 12): How to Feel Great!

Monday, August 15, 2011

'Serial Killer' Cells Demolish Leukemia Tumors

'Serial Killer' Cells Demolish Leukemia Tumors

MIT Researchers Discover New Drug That May Cure Nearly All Viral Infection


By IBTimes Staff Reporter | August 15, 2011 1:02 PM EDT
Researchers at the Massachusetts Institute of Technology, or MIT, have developed what could be a groundbreaking drug that seems effective at curing nearly any viral infection to include the common cold, influenza and other such illnesses.
The drug, dubbed DRACO, or Double-stranded RNA Activated Caspase Oligomerizers, works by targeting a type of RNA produced only in virus-infected cells, and because it's so broad-spectrum, DRACO could potentially be used to fight outbreaks of new viruses, such as the 2003 severe acute respiratory syndrome, or SARS, outbreak, says Todd Rider, who invented the drug, in a statement. Rider is a senior staff scientist in MIT's Lincoln Laboratory's Chemical, Biological, and Nanoscale Technologies Group.
"In theory, it should work against all viruses," Rider says in a statement posted on MIT's Web site.
A paper on the drug can be read in the journal PLoS One.
According to a press release on DRACO, Rider had the idea to try and develop a broad-spectrum antiviral therapy some 11 years ago. This was after inventing CANARY (Cellular Analysis and Notification of Antigen Risks and Yields), a biosensor that can rapidly identify pathogens.
"If you detect a pathogenic bacterium in the environment, there is probably an antibiotic that could be used to treat someone exposed to that, but I realized there are very few treatments out there for viruses," Rider says.
He drew inspiration for DRACO from living cells' own defense systems. Researchers tested the drug against 15 viruses and found it was effective against all of them to include rhinoviruses that cause the common cold, H1N1 influenza, a stomach virus, a polio virus, dengue fever and several other types of hemorrhagic fever.
When viruses infect a cell, they take over its cellular machineryto use for their own purpose. Their purpose is to create more copies of the themselves, and during this process, the viruses make long strings of double-stranded RNA (dsRNA), which isn't found in human or other animal cells, a press release notes.
The human cells, as part of their natural defenses against viral infection, have proteins that latch onto dsRNA, which then sets off a cascade of reactions that prevents the virus from replicating itself. But many viruses can outsmart that system by blocking one of the steps further down that cascade.
So Rider had the idea to combine a dsRNA-binding protein with another protein that induces cells to undergo apoptosis (programmed cell suicide) — launched, for example, when a cell determines it's en route to becoming cancerous. And so, when one end of the DRACO joins to dsRNA, it signals the other end of the DRACO to initiate cell suicide, the press release states.
Karla Kirkegaard, professor of microbiology and immunology at Stanford University, says combining those two elements is a "great idea" and a very novel approach.
"Viruses are pretty good at developing resistance to things we try against them, but in this case, it's hard to think of a simple pathway to drug resistance," she says in a statement.
Researchers say most of the tests reported in this study were done in human and animal cells cultured in the lab, but the they also tested DRACO in mice infected with the H1N1 influenza virus. When mice were treated with DRACO, they were completely cured of the infection. The tests also showed that DRACO itself is not toxic to mice. Researchers are now testing DRACO against more viruses in mice and beginning to get promising results.
Rider says he hopes to license the technology for trials in larger animals and for eventual human clinical trials.