NEW ORLEANSNew research presented at the 92nd Annual
Meeting of the American Association for Cancer Research (AACR) shows that
medulloblastoma, the most common malignant brain tumor in children, is actually
two diseases with distinctly different clinical, pathologic, and genetic
Torsten Pietsch, MD, professor of neuropathology, University of
Bonn, Germany, led the study that differentiated several genetic mutations in a
series of 63 medulloblastomas, including cases of the classic as well as the
desmoplastic (or nodular) variant. Some of the tumors were recently removed
from patients while others came from stored samples.
The same mutations found in desmoplastic medulloblastomas were
not found in patients with the classic type of the disease, he said.
Desmoplastic medulloblastomas are associated with alterations on chromosome 9,
whereas the classic form frequently carries alterations on chromosome 17.
"These findings are significant because they could lead to
a new therapy for one type of medulloblastoma that would directly target the
genetic mechanisms of the disease," he commented. An estimated 400 to 500
children are diagnosed with medulloblastomas each year in the United States.
In desmoplastic medulloblastomas, mutations were found in two
genes, PTCH (patched), located on chromosome 9, and SMOH (smoothened). These
genes help regulate normal development of the brain and other organs as
components of a developmental control signaling pathway. Mutations in either
gene result in overactivation of this pathway, which can lead to uncontrolled
growth of cancer cells (see Figure). This over-activation is not seen in the
classic type of the disease, Dr. Pietsch said.
"The PTCH gene has been known for years to be an important
regulator of cell growth in normal development of embryos. You need this gene
and this pathway for the normal development of many organs, including the
brain," he said.
These alterations are apparently a "very early event"
in these tumors, Dr. Pietsch said at a press conference held in conjunction
with the meeting. He noted that researchers at Johns Hopkins and Stanford have
identified substances that can block the uncontrolled cell growth resulting
from these mutations. "These substances have low toxicity in adult,
nonpregnant animals and can reverse the effects of such mutations in vitro,
possibly leading to future mechanism-based novel treatment strategies," he