A switch to turn off cancer of testis and ovary


LONDON: Researchers from Cambridge have discovered a molecular "switch" that can turn off a highly virulent cancer of the testis and the ovary. The scientists found that all malignant germ cell tumours, like the type which typically occurs in the testes and ovaries, contain large amounts of a protein called LIN28.

This results in too little of a family of tiny regulator molecules called let-7 .

In turn, low levels of let-7 cause too much of cancerpromoting proteins in cells. The cancer-promoting proteins include LIN28 itself, so there is a vicious cycle that acts as an "on" switch to promote malignancy.

The researchers have likened these changes to a "cascade effect" , extending down from the large amounts of LIN28 to affect many properties of the cancer cells. They also discovered that by reducing the amount of LIN28 or by directly increasing the amount of let-7 , it is possible to reverse the vicious cycle.

Both ways reduced levels of the cancer-promoting proteins and inhibited cell growth. Because the level of LIN28 itself goes down, the effects are reinforced and act as an "off " switch to reduce cancerous behaviour.

Cambridge scientists therefore identified the "on/ off " switch and have published their findings in the journal Cancer Research. Malignant germ cell tumours arise in sperms — or egg-forming cells and usually occur in the reproductive organs, the testes or ovaries.

The cancerous tumours are seen in patients of all ages , both in childhood and adulthood. Although many patients do well after treatment , chemotherapy can have severe long-term side effects , including hearing loss and damage to the kidneys.

Scientists grow artificial ear from living tissue


LONDON: Scientists have developed an artificial 'lifelike' ear, using a 3D printer and cartilage from sheep, that works just like the real organ.


Researchers hope the lab-made substitute organs can be used to replace the damaged or missing body parts of patients.

More research and development will be needed before it could be used in clinical transplants on patients, scientists said.

Researchers hope that patients with missing or deformed outer ears, such as kids suffering from a congenital deformity called microtia, might soon be offered living substitutes that could be permanently attached to their heads.

The artificial ear has a key feature in the form of a cartilage scaffold with an embedded titanium wire which retains the shape of the structure as well as maintaining its flexibility, 'The Independent' reported.

"The technology is now under development for clinical trials, and thus we have scaled-up and redesigned the prominent features of this scaffold to match the size of an adult human ear and to preserve the aesthetic appearance after implantation," researchers from the Massachusetts General Hospital in Boston, said.

Researchers formed a collagen connective tissue from a cow into the shape of a human pinna - the fleshy visible part of the ear - and held in place by titanium wire.

They then "seeded" the porous collagen with ear cartilage cells taken from a sheep and the cells grew within the porous collagen fibres.

Scientists grew the ear on mice and rats lacking an immune system to show that it was possible for it to be connected to a blood supply without tissue rejection.

The ear would have to be either made from a patient's own stem cells or used with anti-rejection drugs to be used in a human transplant.

Scientists said a key feature of the technology is that the ear can be designed to look as natural or 'lifelike' as possible by pulling the skin taut over the wire and cartilage frame using vacuum suction.

Monogamy evolved to protect babies


LONDON: The threat of infants being killed by unrelated males is the key driver of monogamy in humans and other primates, according to scientists.

Astudy of 230 primate species by academics from University College London, University of Manchester, University of Oxford and University of Auckland is the first to reveal this evolutionary pathway for the emergence of pair living.

The team found that following the emergence of monogamy males are more likely to care of their offspring. Where fathers care for the young, not only can they protect infants from other males but also share the burden of childcare. Infants are most vulnerable when they are fully dependent on their mother, because females delay further conception while nursing slowly developing young. This leads to the threat from unrelated males, who can bring the next conception forward by killing the infant.

Sharing the costs of raising the young between both parents shortens the period of infant dependency and can allow females to reproduce more quickly.

To uncover the evolutionary pathway that led to monogamy, the team gathered data across the primates. These were then plotted on a family tree of the evolutionary relationships between those species. Computational modelling methods were used to re-run evolution millions of times across the family tree to discover whether different behaviours evolved together and, if so, which behaviour evolved first.

Until now, many hypotheses have been proposed to explain the evolution of monogamy among mammals. These include the benefit of paternal care when the cost of raising offspring is high, the ability to guard solitary females from rival males and protection against the risk of infanticide from rival males.

This "Bayesian" approach allowed the team to determine that male infanticide is the cause of the switch from a multi-male mating system to monogamy in primates. It showed that two-parent care and solitary ranging by females are a result of monogamy , not the cause. "This is the first time that the theories for the evolution of monogamy have been systematically tested, conclusively showing that infanticide is the driver of monogamy," said lead author Dr Kit Opie of University College London. 
 
 
 
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