Thursday, February 14, 2019

Now, reversible antiplatelet therapy to fight clotting, cancer metastasis

Now, a new study published on Wednesday says that a reversible, drug-free antiplatelet therapy could reduce the risk of blood clots and potentially prevent cancer metastasis.

The therapeutic approach involves modifying human platelets to create "decoys" that are still capable of binding to some cells but will not aggregate or carry out the other normal platelet functions, including chemical signalling associated with the clotting process.

Speaking about it, lead author  said, “The reversibility and immediate onset of action are major advantages of our platelet decoys, and we envision them to be useful in hospital-based situations."

She added, "The therapy could prevent clotting in high-risk patients just before they undergo surgery, or be given to cancer patients alongside chemotherapy to prevent existing tumors from spreading."

While platelets play a vital role in halting bleeding and help protecting against minor and life-threatening bleeding, hyperactive platelets can also contribute to various disorders, including severe blood clots, heart disease and cancer.

While several anti-platelet drugs fight clots, their effects are not easily reversible, leaving patients vulnerable if they develop unexpected severe bleeding or are in need of an emergency surgical procedure.

Platelets also play an important part in cancer metastasis by binding to tumour cells and protecting them both from the body's immune system and shear stress as they circulate in the bloodstream. They may also help the cancer cells exit through blood vessels and seed distant tissues during the process of metastasis.

In their journey towards creating decoy platelets, the research team used a detergent treatment and centrifugation to strip natural human platelets of their inner structures and remove their basic activation and aggregation abilities.

These decoy platelets became about one-third the size of a regular platelet while retaining a majority of adhesion receptors on their surface. This allows them to bind to other cells in the bloodstream, such as cancer cells, but not become active during the blood clotting process.

The researchers, first examined how the decoys might impede the formation of blood clots. The team injected the decoys into a microfluidic blood-vessel-mimicking device and observed how the decoys reacted to various platelet-stimulating chemicals.

They found the decoys did not show typical clotting behaviours, and when added to human blood within the device, the normal platelets showed a reduced ability to aggregate and create a clot by binding to the vessel's walls. Furthermore, the researchers quickly reversed the effects of the decoys on normal platelets by introducing fresh platelets into the blood.

Dr. said, “Our ability to reverse the platelet inhibiting effects with a simple reintroduction of normal platelets is very encouraging as currently available anti-platelet agents are often difficult to reverse in emergency settings such as severe bleeding.”

Based on the key role platelets play in supporting cancer metastasis in the bloodstream, the team sought to target circulating tumour cells with their cellular approach. The decoy platelets were able to compete with normal platelets when binding to cancer cells and were effective in preventing cancer cell extrusion out of a vasculature-emulating microfluidic chip model.

Furthermore, in a model of metastasis, there was a significant reduction in the burden of established metastatic tumours when cancer cells were introduced simultaneously with platelets and decoys. 

THIS IS ONLY FOR INFORMATION, ALWAYS CONSULT YOU PHYSICIAN BEFORE HAVING ANY PARTICULAR FOOD/ MEDICATION/EXERCISE/OTHER REMEDIES.                                    PS- THOSE INTERESTED IN RECIPES ARE FREE TO  VIEW MY BLOG-                                                                                           https://gseasyrecipes.blogspot.com/       

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Sunday, January 29, 2017

Altering protein may fight colon cancer progression

Modifying shape of a protein that controls inflammation may reduce progression of inflammatory bowel disease and colon cancer, according to a new study that may pave the way for therapies against the conditions.

The altered protein - IRAK-M - causes the immune system to become supercharged, clearing out the bacteria before they can do any damage.


"When we tested mice with the altered IRAK-M protein, they had less inflammation overall and remarkably less cancer," said Coy Allen, assistant professor at Virginia-Maryland College of Veterinary Medicine in the US.

The next step, he said, will be to evaluate these findings in human patients.

The researchers are also evaluating their findings in laboratory-assembled "mini-guts" - live tissue models that Allen and his team assembled by growing intestinal stem cells on petri dishes to form highly complex small intestinal and colon tissue.

"Ultimately, if we can design therapeutics to target IRAK-M, we think it could be a viable strategy for preventing inflammatory bowel disease and cancer," said Allen.

The study was published in the journal eBioMedicine.


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