Today.Az » Weird / Interesting » Protein May Help Diagnose and Treat Lymphoma in People and Dogs
16 July 2011 [16:51] - Today.Az
A protein that appears to play a key role in the formation of lymphoma and other tumors by inhibiting a tumor-suppressing gene has been identified by a team of veterinary and human medicine researchers at the University of California, Davis.
The researchers suggest that the newly identified protein may be a
potential target for diagnosing and treating lymphoma in humans and
animals. They will report their findings July 15 in the journal Genes & Development.
"Results from this study suggest that a gene known as RNPC1 may play a
key role in the development of lymphoma," said Xinbin Chen, a
veterinary oncologist with appointments in the UC Davis School of
Veterinary Medicine and the UC Davis School of Medicine. Chen led the
study.
About Lymphoma
Lymphoma refers to a group of blood cancers that start in the
lymphatic system, a network of lymph vessels and lymph nodes that play a
vital role in the body's immune system.
Lymphoma occurs when a type of white cell, known as a lymphocyte,
undergoes a malignant change and begins to multiply out of control. As
the lymphocytes multiply rapidly, they eventually crowd out normal,
healthy cells. In time, the cancerous lymphocytes accumulate in the
lymph nodes, liver, spleen and other locations in the body.
Lymphoma occurs spontaneously in dogs, representing 6 percent of all
canine cancers. It is remarkably similar to lymphoma in humans.
Cancer and the P53 Gene
For three decades, researchers have known that a gene referred to as
p53 plays an important role in suppressing cancer. This tumor suppressor
gene checks cells' DNA for mutations that might cause cancer and then
stops cell growth until the mutations can be repaired. If the mutations
can't be repaired, P53 triggers cell death to prevent cancer from
developing.
But if something goes awry, p53 itself can mutate and produce
undesirable proteins. Earlier studies have shown that mutated proteins
produced by p53 are present in 60 percent of all cancerous human tumors.
More recent studies have also shown that p53 can be inactivated in
human cancers by means other than mutation. In short, when p53 and the
process it controls are damaged, cancer often occurs.
In recent years, scientists, including Chen and his colleagues at UC
Davis, have found that p53 mutations also are active in the formation or
cancerous tumors in other mammals, including dogs, cats and horses.
About the RNPC1 gene
Because defects in p53 are so common in human and animal cancers,
researchers have been extremely interested in how the activity of the
gene is regulated. This led the UC Davis team to examine the RNPC1 gene.
RNPC1 is known to be an RNA-binding protein, regulating how other
genes produce proteins. The UC Davis researchers suspected that RNPC1
might play a role in causing lymphomas by inactivating the p53 gene.
Findings from the UC Davis study
In their new study, the researchers examined several types of human
cancer cells as well as cells isolated from a mouse embryo, known as
embryonic mouse fibroblasts.
The team showed that the RNPC1 gene inhibited the activity of the p53
gene and reduced levels of the p53 protein in these cells. Conversely,
p53 protein levels increased when RNPC1 was out of the picture.
Because the RNPC1 gene is located at a chromosome that is frequently
overexpressed in human cancers, including lymphomas, the researchers
examined the expression of RNPC1 in spontaneously occurring dog
lymphomas and in non-cancerous canine lymph node tissue. (The dog lymph
node samples were provided with the permission of the owners; all of the
dogs in the study were patients at the UC Davis Veterinary Medical
Teaching Hospital.)
Data from the dog lymphoma tests showed that the RNPC1 gene is
frequently overactive in dog lymphomas and may, as suspected, play a
role in the formation of lymphomas by inactivating the p53 gene.
Implications for human medicine
"Our findings are consistent with data from other cancer studies,
which showed that RNPC1 is highly expressed in human cancers," Chen
said. "This suggests that further studies are needed to analyze the
expression of patterns of both RNPC1 and p53 in human tumor tissues."
He noted that because dogs and humans alike are vulnerable to
lymphoma, and similar gene processes may be at work in each species, the
dog may serve both as a valuable sentinel for environmental causes of
the disease and as a model for exploring its causes and treatments.
UC Davis is at the forefront of efforts to coordinate animal and
human cancer research to improve cancer treatment for people as well as
pets. The UC Davis Cancer Center's Integrated Cancer Research Program, a
collaboration of more than 200 investigators from more than a dozen
scientific disciplines, includes 19 veterinary oncologists and basic
scientists at the UC Davis School of Veterinary Medicine.
The study was funded in part by the National Institutes for Health.
In addition to Chen, the UC Davis research team included Jin Zhang,
project scientist; Seong-Jun Cho, post doctoral fellow; Limin Shu, post
doctoral fellow; Wensheng Yan, project scientist; Teri Guerrero,
clinical trials coordinator; Associate Professor Michael Kent; and
Assistant Professor Katherine Skorupski; all of the Comparative Cancer
Center, UC Davis Schools of Medicine and Veterinary Medicine; and
Professor Hongwu Chen of the UC Davis Cancer Center. /Science Daily/
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