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Cancer Deaths Could be Reduced by Changes to Newly Found Gene

New gene found that is responsible for the spread of cancer

March 29, 2006 - Scientists at the University of Liverpool have identified a new gene that causes the spread of cancer and speculate that turning off the action of these genes could stop the spread of the primary tumor, which would improve the chances of survival. It is the secondary cancers that are the primary cause of cancer deaths.

 

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Professor Philip Rudland, Dr Guozheng Wang and Dr Roger Barraclough from the University's Cancer and Polio Research Fund Laboratories have discovered an additional member of the S100 family of protein genes – S100P – that causes the spread of cancerous cells from an original tumor to other parts of the body.

If present in the primary tumor, metastagenes such as S100P trigger the rapid spread of cancerous secondary tumors to other tissues in the body via the bloodstream – a process known as metastasis. Although primary tumors can be removed surgically, secondary tumors are more difficult to control. This research has been funded by the Cancer and Polio Research Fund.

The new discovery builds on several years' work carried out at the University to investigate the genes that cause cancerous tumors to travel to other tissues in the body. To date, three other metastasis-inducing genes have been discovered – S100A4, osteopontin, and more recently, AGR2.

 

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Discovery Could Lead to Cancer Prevention

Certain metabolites responsible for initiating breast and prostate cancer

March 29, 2006 - Cancer researchers have discovered that metabolites of natural estrogens can react with deoxyribonucleic acid (DNA) to cause specific damage that initiates the series of events leading to breast, prostate and other human cancers. This understanding of a common mechanism of cancer initiation could result in cancer prevention and in better assessment of cancer risk.

“We have a novel approach to cancer. We know the initiating step,” said Dr. Ercole Cavalieri of the Eppley Cancer Institute, University of Nebraska Medical Center.

“We think prevention of cancer is a problem we can solve by eliminating this initiating step. Estrogens can induce cancer when natural mechanisms of protection do not work properly in our body, and the estrogen quinones are able to react with DNA. In fact, if these protections are insufficient, due to genetic, lifestyle or environmental influences, then cancer can result.

“Now that we have the basic knowledge about a unifying mechanism of cancer initiation, we have a greater sense of urgency to assess people at risk and, at the same time, begin prevention by using specific natural compounds.”

The study describes how the catechol estrogen quinones react with DNA to produce specific mutations that may trigger breast, prostate and other human cancers. 

 “We’ve known about these catechol estrogen quinones for a long time, through many different studies that we’ve done, but our most recent results have been quite decisive,” said Dr. Eleanor Rogan of the University of Nebraska Medical Center. “It’s very big news. From here, we will use the information to ultimately try to prevent breast and prostate cancer.”

The researchers will present their findings at the 81st annual meeting of the Southwestern and Rocky Mountain Division of the American Association for the Advancement of Science  (SWARM-AAAS) on Friday, April 7, at the University of Tulsa, in Tulsa, Okla. 

 

Chemotherapy and radiotherapy are often the only options available to treat secondary tumors but these procedures can be problematic to the patient as they can damage other healthy tissue and do not always succeed in eradicating the cancer.

S100P is commonly found in ten different types of normal tissue including the placenta, spleen, colon, ovary, prostate, lung and heart. Scientists believe proteins like S100P function in healthy tissue by increasing the movement of white blood cells around the body. If the protein is found in a cancerous tumor however, it causes the tumor to spread to other tissues.

Professor Rudland said: "It is the spread of cancer from the initial tumor that is the key contributor to death of a cancer patient. Metastagenes are fundamental to this process and can be found in most common cancers, including breast, lung and colon. If these genes are over-expressed in the cancerous tumor, early death of the patient is much more likely.

"The next major step is to develop drugs that will switch off the action of these genes. If we can do this, we can stop the spread of the primary tumor and therefore improve the chances of survival for patients.

"We are grateful for the support given by the Cancer and Polio Research Fund."

The research is published in the current edition of Cancer Research.

About source:

The University of Liverpool is one of the UK's leading research institutions. It attracts collaborative and contract research commissions from a wide range of national and international organizations valued at more than £90 million annually.

The Cancer and Polio Research Fund is a charity based on the Wirral that funds research nationwide into cancer and other crippling diseases. In the 43 years of its existence, it has spent more than £35 million on a wide range of medical research projects and the provision of equipment and facilities. It is entirely dependent on charitable donations for its income. For more information please contact Roger Thornhill on 01948 667 729.

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