William Atkins
Sunday, 13 April 2008 21:24
Science -
Health
Page 1 of 2
One dose of the early-stage experimental drug protected mice and monkeys from lethal doses of radiation. Future experiments will be conducted to see if tissues in humans can, likewise, be protected during radiation treatments and as an antidote from nuclear attacks.
Andrei V. Gudkov, who is chairperson of Cell Stress Biology within the
Roswell Park Cancer Institute (Buffalo, New York, U.S.A.), was the lead researcher in the study.
The drug of interest has been named CBLB502, a polypeptide drug derived from
Salmonella flagellin.
In the past and still today, radiation is a quite useful medical tool in combating diseases such as cancer by destroying cancerous cells. However, the radiation can also adversely affect healthy tissues, bone marrow, the gastrointestinal (GI) tract, and other such areas of the human body.
Because of the problems caused to normal cells, the amount and number of radiation treatments must be limited.
If this drug proves to be effective at protecting such healthy cells from radiation, it will be very important for future radiation treatments. However, other drugs have also been studied in the past, and they failed to live up to expectations.
The Gudkov team developed the drug related to the process called apoptosis. The process is the body’s natural (pre-programmed) way to stop defective cells from spreading to healthy cells. This activity called programmed cell death (PCD) occurs in all multicellular organisms.
However, apoptosis is prevented from occurring in cancer; that is, bad cells are killed but good cells are also adversely affected. Thus, it causes cancerous tumors to occur.
Gudkov and his team found that when apoptosis is prevented from occurring a pathway called “nuclear factor-KappaB” (NFKB) is also blocked.
The NFKB pathway is activated by flagellin, a protein in gut bacteria, and is normally used by apoptosis to destroy bad cells while leaving good cells alone.
Once the Gudkov team learned of the connection among apoptosis, NFKB, and flagellin, they decided to try to simulate the same pathway. Gudkov called their simulation a “tumor trick.” [Associated Press]
Consequently, they created a drug derived from the flagellin protein.
They injected the drug CBLB502 into mice and rhesus monkeys, waited from fifteen to sixty minutes, and then exposed the laboratory animals to lethal doses of radiation.
The investigators found that the drug improved survival rates, helping to protect bone marrow and the GI tract. The animals had more protection when the wait time was 60 minutes versus shorter times.
Especially important for radiation treatments for cancer patients, the drug CBLB502 did not prevent radiation from treating tumors in the mice as it protected healthy tissues.
As an added plus, the U.S. government is interested in the drug in order to protect its citizens against possible nuclear attack. Please read on for additional information. The abstract to the Gudkov paper is also included.