New Treatment for "Untreatable" Progeria Syndrome has Roots in "Untargeted" Basic Cell Biology Research
FOR IMMEDIATE RELEASE:
ASCB posts background file on basic biology discoveries behind Boston Children’s clinical trial reporting significant slowing of rare rapid aging disorder in children.
BETHESDA, MD, SEPTEMBER 25, 2012---The good news widely reported this morning of positive results from a clinical drug trial at Boston Children’s Hospital for the previously “untreatable” rapid aging disorder in children known as progeria has its scientific roots in basic biology discoveries made in recent years.
A paper published Monday in the Proceedings of the National Academy of Sciences (PNAS) reports that the use of farnesyl transferase inhibitors (FTI) significantly slows the progress of progeria, a rare and until now “untreatable” lethal genetic disorder. Also known as Hutchinson-Gilford Progeria Syndrome (HGPS), progeria has been described as out-of-control rapid aging in children. A “normal” baby born with HGPS will stop growing by 16-18 months and quickly develop signs of old age including hair loss, thin skin, osteoporosis and, most dangerously, progressive arteriosclerosis. By 10 years of age progeria children appear to be 80. The PNAS paper apparently shows a significant slowing of bone loss and blood vessel blockage.
This clinical trial grew out of the identification of the defective progeria gene, LMNA, in 2003 through the Human Genome Project and the laboratory of current NIH Director Francis Collins. But the link to defective proteins called lamins that make up the envelope surrounding the cell nucleus came about through “untargeted” basic cell biology research. Veteran lamin researchers remember having their grant applications dismissed by review panels as “boring” and irrelevant. But basic work by Robert Goldman of the Northwestern University School of Medicine and other nuclear lamin researchers around the world revealed that a greasy tag molecule called farnesyl accumulates on defective Lamin A proteins, eventually warping the structure of the entire nuclear envelope and disrupting the orderly production of genetic messages in the nucleus that direct normal growth.
The identification of the defective LMNA gene transformed progeria into a “laminopathy,” a now growing class of diseases caused by problems with the once-irrelevant nuclear lamins. “Normal” aging is thought to involve many of the same processes as laminopathies and gives this new clinical trial implications beyond progeria. With the discovery of the lamin link, clinical researchers were suddenly looking for farnesyl transferase inhibitors (FTI) for progeria treatment. They zeroed in on Lonafarnib, an FTI drug developed by Merck that had been extensively tested and found safe for use in adults and children but ineffective against its brain cancer targets. In the two and a half year clinical trial, physicians at Boston Children’s gave Lonafarnib to 26 children with progeria.
The American Society for Cell Biology has been reporting on progeria since 2006. In 2008, the ASCB Newsletter published a report on the proposed clinical drug trial. The ASCB has pulled together a file of these earlier reports for reporters and the general public interested in the deeper scientific background of progeria.