Monday | 24 November, 2008
Australian Biotechnology News
p53 regulates drug sensitivity
‘Guardian of the genome’ predicts treatment outcomes for childhood cancer.
Staff Writers 05/11/2007 11:50:55

Australian researchers have identified a new role for a cancer-prevention gene in the response to drug treatment for childhood cancer.

In humans, the p53 tumour suppressor gene, also known as the 'guardian of the genome', is known for its role in the prevention of cancer.

Mutations in the gene are associated with a high incidence of cancer due to the uncontrolled division of cells which give rise to tumours.

In childhood cancers such as neuroblastoma, p53 mutations are rare at diagnosis, but they can emerge after chemotherapy.

In a study published in the international journal Cancer Research this month, researchers from the Children's Cancer Institute Australia for Medical Research (CCIA) and collaborators in the USA, describe a new role for p53 in childhood cancer.

The group showed that by inactivating p53 in neuroblastoma cells, the most common childhood cancer, the cancer cells became resistant to a number of chemotherapy drugs.

"Our results provide definitive evidence of a role for p53 as a gene which dictates drug sensitivity in neuroblastoma," lead author Dr Chengyuan Xue, of CCIA's molecular diagnostics program, said.

"These results highlight the importance of p53 status as an indicator of a patient's treatment response in neuroblastoma."

Further research has found that p53 does not have one defined function in cancer susceptibility to treatment, he said.

"In some cancer cell types it does not act as a drug sensitivity gene. It is therefore important to assess the clinical effect of p53 mutations in different cancers in a tissue context."

Source: CCIA

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Comments

P53 Mutation

We have to mutation in the p53 gene because this protein sequence more hydrophilic group is there so we can alter the particular place in to hydrophophic aminoacids so those aeras we can alter then we can avoid all cancer . i m doing this porject
now. my worksgenome based solving disease.

 
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