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Scientists discover clue to growing new breast tissue

 
 

A FULLY functional breast has been grown from a stem cell found in female mice, in a study that promises insights into recurring breast tumours and a fresh approach to plastic surgery.

The research in Australia suggests that breast cancers may be triggered by rogue mammary stem cells that are difficult to kill with standard chemotherapy, and that later “reseed” the breast with tumour cells once a patient appears to be in remission.

If the findings prove applicable to people, scientists hope to develop drugs that target abnormal breast stem cells to eliminate not only tumours but also the source tissue from which they arise. In the longer term, it may also be possible to use mammary stem cells to grow breast tissue for reconstructive surgery after a mastectomy, or even for use in breast enhancement operations.

In the study, which is published today in the journal Nature, a team led by Jane Visvader, of the Walter and Eliza Hall Institute in Melbourne, isolated mammary stem cells from the breast pads of female mice for the first time.

They transplanted one of these cells into the mammary fat pad of a living female mouse from which all breast tissue had been removed. The cell divided and eventually gave rise to all the normal types of cell found in the mouse breast, and the gland worked normally to produce milk.

Researchers suspect that mammary stem cells play an important role in the genesis of some breast cancers. If a stem cell carries genetic errors, it may start producing cancerous breast cells, in effect becoming a “tumour factory”. This may be why some breast cancers return after apparently being eliminated by chemotherapy.

Chemotherapy targets fast-dividing cancer cells, but the stem cells may prove more resistant as they do not reproduce so quickly. This would mean that, although the primary breast cancer is killed by the treatment, abnormal stem cells are left behind to continue turning out cancer cells, restarting the tumour.

“The ultimate objective is to create a drug that will, in effect, switch off breast cancer cells,” Dr Visvader said. “To do this, the exact make-up of genes expressed by normal and rogue stem cells will need to be determined. Then a drug will be designed to engage with and neutralise the faulty feature of the stem cell.”

The team is now examining tissue from human breast tumours, to determine whether they share characteristics with the mouse model. A second team, from the British Columbia Cancer Research Centre in Vancouver, has also isolated mammary stem cells and published its work today in Nature.

The research could also have implications for plastic surgery. If women have similar breast stem cells, it may eventually be possible to grow them into breast tissue. This could be used to reconstruct the breasts of cancer patients who have had a mastectomy, or even to grow implants for augmentation operations.

  • Women who have breast cancer surgery fare much better if the surgeon has had plenty of practice, research by a team from Guy’s Hospital in London shows. The study of 1,351 women in South Korea, published in the International Journal of Clinical Practice, found that 95 per cent of those readmitted to hospital after surgery had been treated at units doing fewer than 100 such procedures a year.

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    Prostate cancer: the clue to its origins?

    Research suggests that stem cells play a leading role, opening up the possibility of new treatments
     
    Could scientists have discovered the clue to what makes prostate cancer grow? That’s the suggestion being made by researchers at York University, who have found the cells that appear to “drive” prostate cancer by ordering surrounding cells to turn malignant, and have been able to grow these cells in the laboratory. This raises the possibility that pharmaceutical companies could develop treatments to kill the offending “ parent” cells.
     
    The “parent” cells are actually stem cells. Healthy stem cells act as the building blocks of life, giving rise to a range of cells responsible for regenerating our organs, tissues and red blood cells. Now cancer specialists say that stem cells may play a leading role in prostate cancer, too.

    This week scientists at the Yorkshire Cancer Research Unit, led by Professor Norman Maitland and Dr Anne Collins, both biologists, have reported that cancer stem cells work in a similar way to healthy stem cells. Writing in the American journal Cancer Research, they say that although only 0.1 per cent of the cells they took from prostate tumours were cancer stem cells, this small number had been able to direct other, lesser cells to develop into “colonies” of tumours four times their own number.

    This is “groundbreaking” work, according to Jack Schalken, professor of experimental urology at Radboud University in the Netherlands. He says: “Identifying the cancer stem cell is the most important element: stem cells feed the whole repertoire of cancer cells that complete the tumour.”

    Hing Leung, professor of urological oncology at Newcastle University, says that the concept of cancer stem cells is “the equivalent of finding the ‘engine room’ that drives cancer to grow, spread and resist treatment such as chemotherapy and radiotherapy”. He adds: “Finding such stem cells is like looking for a very small needle in a rapidly growing haystack. This study has identified the first ‘hints’ that such novel stem cells do exist in prostate cancer.

    “This is likely to open up new avenues to understand better the underlying biology of cancer. It may also highlight ‘drugable’ targets for developing better medicine.”

    Professor Maitland explains that most cancer treatments try to kill off the bulk of tumour cells, leaving behind a stem cell population. But if you can kill the roots, “you kill the cancer for good”.

    Professor Schalken suggests that Professor Maitland’s work will be the catalyst for treatments that may, in time, have a similar impact to the development of hormone therapy in the 1950s. Until then, the only treatment for prostate cancer was surgery.

    Professor Maitland is cautious about when a treatment might become available but believes that cyclopamine, a drug undergoing human trials in the US, could be “a ready-made therapy” because it has been shown to reduce tumours, possibly by preventing stem cells from communicating with surrounding cells.

    Until now the drug has been used blind, says Professor Maitland. Researchers have not been able to target it at the cancer stem cells, which can mean that it has the potential to kill the normal, healthy stem cells that renew our bodies. This is clearly a problem because without stem cells organs such as the liver would shrivel up.

    Both professors are wary of raising false hopes, but Professor Maitland suggests that at a time when treatments are developed more and more quickly, an effective treatment could be only years away.

    Chris Hiley, head of research at the Prostate Cancer Charity, says: “The research and discoveries in prostate cancer stem cells are exciting.

    “There is usually the fear that scientists can overstate their findings, but Professor Maitland is a very measured researcher and is clued up about making his findings relevant for patients suffering with prostate cancer. It is very promising.”

     


    Hot chili peppers might help fight prostate cancer: study

    A woman sells chilli peppers at a market
    Capsaicin, the heat-generating element in the chili peppers that delights spicy food lovers around the world, causes prostate cancer cells to kill themselves, researchers said.
    A team of US cancer scientists found in tests on mice that capsaicin could provoke apoptosis, or programmed cell death, in the cells behind human prostate cancer, the most common cancer among men in the United States.
    According to the scientists at the Samuel Oschin Comprehensive Cancer Institute at Cedars-Sinai Medical Center in Los Angeles, the tests showed the potential of repressing the growth of the cancer cells in humans.
    "Capsaicin had a profound anti-proliferative effect on human prostate cancer cells in culture," said the institute's Soren Lehmann.
    "It also dramatically slowed the development of prostate tumors formed by those human cell lines grown in mouse models," he said.
    To conduct their test, the researchers fed the heat-generating alkaloid found in all types of chilis orally to mice. Lehmann said the dose was equivalent to a 200 pound (90 kilogram) man eating from three to eight of the ultra-hot habanero peppers three times a week.
    The heat of habanero peppers registers up to 300,000 Scoville units, compared to a maximum of 5,000 Scoville units for jalapenos and 175,000 for bird chilis popular in Southeast Asia and Africa, according to the Chile Pepper Institute of New Mexico State University.
    Lehmann's research team found that the capsaicin interfered with the cancer cells' ability to avoid apoptosis, which occurs normally in many tissues as they replace aged cells with new ones.
    Cancer cells are able to mutate or change genes to avoid a programmed dying off.
    The team found that the doses of capsaicin induced about 80 percent of prostate cancer cells to move toward apoptosis.
    Prostate cancer kills about 221,000 people worldwide every year.

     

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