Tag Archives: cell

How To Eradicate Breast Tumors In 11 Days

Despite unbelievable advances in medical science in recent decades, breast cancer kills. Approximately 1 in 8 American women will develop breast cancer cells during the course of their lifetime.

Finding a cure is imperative, and as such, fervent research continues. At the European Breast Cancer Conference in Amsterdam, scientists presented a pair of drugs with an astounding claim: this treatment can eradicate some types of breast cancer in only 11 days, eliminating the need for chemotherapy.

Chemotherapy, whilst an amazing feat of medical-scientific engineering, is known for its uncomfortable and sometimes debilitating side effects. Women undergoing chemotherapy for breast cancer treatment may lose their hair, suffer extreme fatigue, and even loss of cognitive functionCancers may also recur after long, painful months of chemotherapy treatment.

The new trial, raising hopes across the medical community, is focused upon two drugs: Herceptin and Lapatinib. The drugs, in tandem, target a protein known as HER2, which is instrumental in stimulating the growth of certain cancer cells.

A pair of drugs can dramatically shrink and eliminate some breast cancers in just 11 days, UK doctors have shown.

They both target HER2 – a protein that fuels the growth of some women’s breast cancersHerceptin works on the surface of cancerous cells while lapatinib is able to penetrate inside the cell to disable HER2.

The study, which also took place at NHS hospitals in Manchester, gave the treatment to women with tumours measuring between 1 and 3cm. But Prof Bliss believes the findings could eventually mean some women do not need chemotherapy.

In less than two weeks of treatment, the cancer disappeared entirely in 11% of cases, and in a further 17% they were smaller than 5mm.

Current therapy for HER2 positive breast cancers is surgery, followed by chemotherapy and Herceptin. But Prof Bliss believes the findings could eventually mean some women do not need chemotherapy.

Source: https://www.bbc.com

How To Manipulate And Move Cells With Light

Wits physicists demonstrate a new device for manipulating and moving tiny objects with light. When you shine a beam of light on your hand, you don’t feel much, except for a little bit of heat generated by the beam. When you shine that same light into a world that is measured on the nano– or micro scale, the light becomes a powerful manipulating tool that you can use to move objects around – trapped securely in the light.

Researchers from the Structured Light group from the School of Physics at the University of the Witwatersrand in Johannesburg, South Africa, have found a way to use the full beam of a laser light, to control and manipulate minute objects such as single cells in a human body, tiny particles in small volume chemistry, or working on future on-chip devices. While the specific technique, called holographic optical trapping and tweezing, is not new, the Wits Researchers found a way to optimally use the full force of the light – including vector light that was previously unavailable for this application. This forms the first vector holographic trap.

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Previously holographic traps were limited to particular classes of light (scalar light), so it is very exciting that we can reveal a holistic device that covers all classes of light, including replicating all previous trapping devices,” explains Professor Andrew Forbes, team leader of the collaboration and Distinguished Professor in the School of Physics where he heads up the Wits Structured Light Laboratory.

What we have done is that we have demonstrated the first vector holographic optical trapping and tweezing system. The device allows micrometer sized particles, such as biological cells, to be captured and manipulated only with light.”

Source: https://www.wits.ac.za/

New Hope To Fight Alzheimer’s

It is known that the onset of Alzheimer’s disease (AD) is associated with the accumulation of Amyloid beta () peptides in small molecular clusters known as oligomers. These trigger the formation of so-called ‘neurofibrillary tangles’ within neurons hamper their workings, ultimately causing cell death and so significant cognitive decline. Very large Aβ oligomers which form plaques outside neurons, alongside neuroinflammation have also been found to play a key part in the progression of the disease.


The EU-funded iRhom2 in AD project took as its starting point the protein iRhom2, which has been identified as a genetic risk factor for AD due to its pro-inflammatory properties. The team were able to explore further the influence of iRhom2 on neuroinflammation in mice. iRhom2 recently emerged as a protein of note in AD as it aids the maturation of an enzyme called TACE (tumor necrosis factor-α converting enzyme) guiding it towards a cell’s plasma membrane where the enzyme releases a cell-signalling cytokine (TNFα), implicated in the regulation of inflammatory processes. While mice studies have shown that TNFα-dependent inflammation can lead to sepsis and rheumatoid arthritis, it is also thought that the process contributes to neuroinflammatory signalling events, which can cause harm in the brain.

The EU-funded iRhom2 in AD project worked with mice that are prone to develop the hallmarks of AD, amyloid plaques and memory deficits. The team genetically altered iRhom2 in the mice then analysed the progression of the pathology using an array of biochemical and histological methods, together with a number of behavioural tests to assess cognitive decline. The results were somewhat surprising.

We initially hypothesised that iRhom2 would affect one specific aspect of neuroinflammation in AD. What we discovered was even more exciting as it actually affects several different aspects of neuroinflammation simultaneously. So modulating iRhom2 appears particularly well suited to interfere with AD,” explains project coordinator Prof. Dr. Stefan Lichtenthaler.

Source: https://cordis.europa.eu/

Brain Metals Drive Alzheimer’s Progression

Alzheimer’s disease could be better treated, thanks to a breakthrough discovery of the properties of the metals in the brain involved in the progression of the neurodegenerative condition, by an international research collaboration including the University of Warwick.

Iron is an essential element in the brain, so it is critical to understand how its management is affected in Alzheimer’s disease. The advanced X-ray techniques that we used in this study have delivered a step-change in the level of information that we can obtain about iron chemistry in the amyloid plaques. We are excited to have these new insights into how amyloid plaque formation influences iron chemistry in the human brain, as our findings coincide with efforts by others to treat Alzheimer’s disease with iron-modifying drugs,” commented Dr Joanna Collingwood, from Warwick’s School of Engineering, who was part of a research team which characterised iron species associated with the formation of amyloid protein plaques in the human brainabnormal clusters of proteins in the brain. The formation of these plaques is associated with toxicity which causes cell and tissue death, leading to mental deterioration in Alzheimer’s patients.

They found that in brains affected by Alzheimer’s, several chemically-reduced iron species including a proliferation of a magnetic iron oxide called magnetite – which is not commonly found in the human brainoccur in the amyloid protein plaques. The team had previously shown that these minerals can form when iron and the amyloid protein interact with each other. Thanks to advanced measurement capabilities at synchrotron X-ray facilities in the UK and USA, including the Diamond Light Source I08 beamline in Oxfordshire, the team has now shown detailed evidence that these processes took place in the brains of individuals who had Alzheimer’s disease. They also made unique observations about the forms of calcium minerals present in the amyloid plaques.

The team, led by an EPSRC-funded collaboration between University of Warwick and Keele University – and which includes researchers from University of Florida and The University of Texas at San Antonio – made their discovery by extracting amyloid plaque cores from two deceased patients who had a formal diagnosis of Alzheimer’s. The researchers scanned the plaque cores using state-of-the-art X-ray microscopy at the Advanced Light Source in Berkeley, USA and at beamline I08 at the Diamond Light Source synchrotron in Oxfordshire, to determine the chemical properties of the minerals within them.

Source: https://warwick.ac.uk/