MicroRNA-210 Stabilizes Atherosclerotic Plaques

Researchers here find a way to stabilize the fatty plaques that form in blood vessels as a part of atherosclerosis. On its own this is a pretty poor treatment option, better than nothing, but worse than any approach that removes plaques or prevents them from forming. It will probably be a useful adjunct to any form of removal or reduction of plaque, however, helping to avoid rupture of larger sections of plaque during that process. It is the disintegration of fragile plaques that makes atherosclerosis lethal, as the fragments can then block critical blood vessels to cause a stroke or heart attack.

The molecule microRNA-210 stabilises deposits in the carotid artery and can prevent them from tearing. Thus, it may prevent dangerous blood clots from forming. The most common cause for the narrowing of the carotid artery is atherosclerosis, where so-called plaques build up on the vessel walls. If a plaque ruptures, blood clots can form that either further occlude the site that is already narrowed, or are carried away by the blood flow, which could lead to vascular occlusion at a different site. If this happens in the carotid artery, it could lead to a stroke. How easily a plaque ruptures depends on how thick the tissue layer surrounding its core is. The thicker this fibrous cap, the more stable and therefore more harmless the vessel deposit.

"New imaging procedures enable us to detect dangerous plaques with increasing precision; but the therapies currently available for removing these unstable plaques and thus preventing a stroke entail a certain amount of risk that the plaques will rupture during the procedure. This is why these therapies are not used on individuals with a narrowed carotid artery who have so far not experienced any symptoms. Traditionally, physicians try to reduce the size of the deposits in the vessels in order to widen the narrowed sites. For narrowed carotid arteries, though, the notion of stabilising the plaques is becoming ever more prevalent. Unlike in the coronary vessels, in the carotid artery plaques rupturing is more dangerous than the narrowing."

Researchers compared material from patients with stable and unstable deposits in the carotid artery. They particularly focused on microRNAs. These molecules are involved in the gene regulation in about 60 percent of mammals' genes. They can prevent gene information that has already been read from being translated into proteins, and have become a focus of biomedical research as active ingredients and starting points for new therapies in recent years. The scientists discovered that microRNA-210 was reduced the most in the blood samples of patients with unstable plaques. These were blood samples that were obtained locally near the vessel deposits. Further examinations showed that microRNA-210 is primarily present in the fibrous caps of plaques and that it inhibits the expression of the APC gene. As a consequence, fewer smooth muscle cells die in the fibrous cap and it becomes more stable. Moreover, the animal model could show that fewer plaques rupture when microRNA-210 is administered.

The scientists are currently researching how microRNA-210 can be applied locally. The risk of adverse events in other organs is much too high if microRNA modulators are administered systemically. The main concern with microRNA-210 is that tumour cells that are possibly already in existence will multiply, because the expression of APC is inhibited. This is because APC is a tumour suppressor gene which inhibits the growth of tumours in the healthy body. In order to avoid such off-target effects, the researchers are currently testing coated stents or balloons that are inserted directly into the carotid artery.

Link: https://www.tum.de/en/about-tum/news/press-releases/detail/article/33846/

Comments

HEy !

This is an Incredible advancement ! Bravo !!! I suffer from this deadly disease and have ischemic bouts of pain sometimes because of atherosclerosis (your arteries 'choke' and it's as if someone snap them like twigs, it's horrifying you feel you could die any moment).

Stabilizing them from breaking and forming the clot is so - Crucial, it's what saved my life. PLaques are very unstable and any stressful situation increases ischemia attack/thrombosis. It's better to remove them, but if for now it's all we can do 0 still better than nothing.

The next step : nanobacterias targeted towards plaques - remove that, like nanorobots would do, since the macrophages are pretty much useless/inflammatory and contribute to atherosclerosis when oxidized cholesterol LDL/vLDL/vsLDL accumulated in atherosclerotic lesions by producing ROS.

In the mean time the only saving grace - reducing your Total cholesterol at all costs. This will save your life (like it did for me, it's the oxidized cholesterol that creates this unstability/plaque rupturing by the oxidative ROS stress it creates. So of course less cholesterol less plaque rupturing/plaque forming/atherosclerosis reversal; I'm a living proof,
start your cholesterol abolition diet the Fastest you can, it will make Major difference between you dying of, or surviving, atherosclerosis).

Posted by: CANanonymity at April 14th, 2017 12:13 PM

PS: or use the calcium carbonate nanoparticles method (although I'm not so sure about this because atherosclerotic plaque are calcium rich/show Calcification).

''CD9 monoclonal antibody-conjugated lactose-wrapped *calcium carbonate nanoparticles* loaded with rapamycin (CD9-Lac/CaCO3/Rapa) were prepared for targeted rapamycin delivery to senescent cells. The nanoparticles exhibited an appropriate particle size (~130 nm) with high drug-loading capacity (~20%). In vitro drug release was enhanced in the presence of β-galactosidase suggesting potential cargo drug delivery to the senescent cells''

Posted by: CANanonymity at April 14th, 2017 12:22 PM

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