Cells responsible for cancer relapse identified

Aug 2, 2012
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London: In a breakthrough expected to develop a ‘real cure’ for cancer, scientists claimed to have identified cells that cause tumours to grow and are resistant to chemotherapy and radiotherapy causing cancer to relapse.
Researchers from Cancer Research UK and University of Texas in separate studies found that the growth and life of a tumour is dependent on one small group of cells, known as cancer stem cells, the Daily Mail reported.
Cells that make cancer come back have been identified. Reuters.
The cells fuel the disease’s spread around the body and are believed to be resistant to radiotherapy and chemotherapy and are responsible for cancers coming back after treatment. Until now, it was not proven that they exist in tumours.
Scientists claimed that combining a drug that attacks these cells with current treatments could lead to a cure. Ben Simons, from the Cancer Research UK’s Cambridge Research Institute said that knowing just which cells to target “might be a much better strategy to effect a real cure and prevent relapse”.
Simons’s study tracked the development of skin cancer in mice. By tracking individual cells, it showed a small number of them drive the growth of the tumour.
A second study identified a group of cells that allow the most common type of brain tumour to regrow after chemotherapy. University of Texas researcher Luis Parada found that killing the stem cells, with the help of genetic wizardry, stopped the brain tumours from growing any further in mice. The study was published in journals Nature and Science.
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Cholesterol-lowering drugs can help in asthma treatment: study


 
Asthma
Asthma patients who take cholesterol-lowering drugs alongside inhaled corticosteroids are half as likely to require hospital attention, a new study has claimed.
Researchers at the University of Mississippi found that statins which have anti-inflammatory properties could be helpful in treating asthma which is an inflammatory condition, a news report said.
"We know statins have uses beyond the treatment of heart conditions. They have anti-inflammatory properties, which means they have other as yet mostly unexplored purposes. Asthma is an inflammatory condition so there is clearly a link," consultant physician Dr Shahid Hamid, at Princess Royal University Hospital in Kent said.
The research studied 479 patients on statins and inhaled corticosteroids, and 958 just taking corticosteroids. At least one asthma-related hospitalisation was observed in 3.79 per cent of the first group, compared with 6.47 per cent of the second group.
"This is the most promising study yet, doctors are aware patients admitted to hospital with pnuemonia have a better prognosis if given statins," he was quoted by the paper as saying.
However, there has been controversy about taking statins for asthma and they may have unpleasant side effects.
"It is still too soon to start prescribing statins as a matter of course," Hamid said.

Discovery of New White Blood Cell Reveals Target for Better Vaccine Design

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ScienceDaily (July 27, 2012) — Researchers in Newcastle and Singapore have identified a new type of white blood cell which activates a killing immune response to an external source -- providing a new potential target for vaccines for conditions such as cancer or Hepatitis B.
Publishing in the journal Immunity, the team of researchers from Newcastle University in collaboration with A*STAR's Singapore Immunology Network (SIgN) describe a new human tissue dendritic cell with cross-presenting function.
Dendritic cells (DCs) are a type of white blood cell that orchestrate our body's immune responses to infectious agents such as bacteria and viruses, as well as cancer cells. They are also very important for eliciting the immune response generated by vaccines.
DCs kick start an immune response by presenting small fragments of molecules from micro-organisms such as bacteria and viruses, or from vaccines or tumours, called antigens on their surface. This leads to activation of another white blood cell subset called T cells, which specialise in killing cells and are crucial for eliminating cancerous or infected cells. Most cells are only able to present antigens from within themselves, and so will only elicit an immune response if they are infected themselves. Only a specialised subset of DCs is able to generate a response to an external source of antigen, for example bacteria, vaccines and tumours.
The identity of human tissue DCs that are capable of presenting external antigen to activate the cell-killing response by T cells -- a process termed 'cross-presentation' -- has remained a mystery. Their discovery, as revealed by this research, will help scientists to design better targeted vaccine strategies to treat cancer and infections such as Hepatitis B.
"These are the cells we need to be targeting for anti-cancer vaccines," said Dr Muzlifah Haniffa, a Wellcome Trust Intermediate Fellow and Senior Clinical Lecturer at Newcastle University. "Our discovery offers an accessible, easily targetable system which makes the most of the natural ability of the cell." The researchers also showed for the first time that dendritic cell subsets are conserved between species and have in effect created a map, facilitating the translation of mouse studies to the human immune system.
"The cross-species map is in effect a Rosetta stone that deciphers the language of mouse into human," explains Matthew Collin, Professor of Haematology from Newcastle University.
In the paper the researchers describe how the cross-presenting DCs were first isolated from surplus plastic surgery skin which was digested to melt the gelatinous collagen to isolate the cells. This research will have significant impact on the design of vaccines and other targeted immunotherapies.
The Rosetta Stone of our immune system: Mapping Human and Mouse dendritic cells
The Newcastle University team in collaboration with A*STAR's Singapore Immunology Network (SIgN) have for the first time ever aligned the dendritic cell subsets between mouse and humans allowing the accurate translation of mouse studies into the human model for the first time.
The researchers isolated the dendritic cells from human blood and skin and those from mouse blood, lung and liver. Using gene expression analysis, they identified gene signatures for each human dendritic cell subset. Mouse orthologues of these genes were identified and a computational analysis was performed to match subsets across species.
This provides scientists for the first time with an accurate model to compare DCs between species. Professor Matthew Collin explains: "This is in effect a Rosetta stone that deciphers the language of mouse into human. It can put into context the findings from the extensive literature using mouse models to the human settings."
Dr. Haniffa added: "These gene signatures are available in a public repository accessible for all researchers to benefit from the data. It will allow detailed knowledge of individual human dendritic cell subsets to enable specific targeting of these cells for therapeutic strategy."
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