Summary: 15 newly discovered “hotspots” in the genome that either speed up or slow down brain aging could be new targets for the development of Alzheimer’s medications and therapies for other brain disorders.
Source: USC
Researchers from a USC-led consortium have discovered 15 “hotspots” in the genome that either speed up brain aging or slow it down—a finding that could provide new drug targets to resist Alzheimer’s disease and other degenerative brain disorders, as well as developmental delays.
In machine learning, understanding why a model makes certain decisions is often just as important as whether those decisions are correct. For instance, a machine-learning model might correctly predict that a skin lesion is cancerous, but it could have done so using an unrelated blip on a clinical photo.
While tools exist to help experts make sense of a model’s reasoning, often these methods only provide insights on one decision at a time, and each must be manually evaluated. Models are commonly trained using millions of data inputs, making it almost impossible for a human to evaluate enough decisions to identify patterns.
Now, researchers at MIT and IBM Research have created a method that enables a user to aggregate, sort, and rank these individual explanations to rapidly analyze a machine-learning model’s behavior. Their technique, called Shared Interest, incorporates quantifiable metrics that compare how well a model’s reasoning matches that of a human.
Whether a computer could ever pass for a living thing is one of the key challenges for researchers in the field of Artificial Intelligence. There have been vast advancements in AI since Alan Turing first created what is now called the Turing Test—whether a machine could exhibit intelligent behavior equivalent to, or indistinguishable from, that of a human. However, machines still struggle with one of the fundamental skills that is second nature for humans and other life forms: lifelong learning. That is, learning and adapting while we’re doing a task without forgetting previous tasks, or intuitively transferring knowledge gleaned from one task to a different area.
Now, with the support of the DARPA Lifelong Learning Machines (L2M) program, USC Viterbi researchers have collaborated with colleagues at institutions from around the U.S. and the world on a new resource for the future of AI learning, defining how artificial systems can successfully think, act and adapt in the real world, in the same way that living creatures do.
The paper, co-authored by Dean’s Professor of Electrical and Computer Engineering Alice Parker and Professor of Biomedical Engineering, and of Biokinesiology and Physical Therapy, Francisco Valero-Cuevas and their research teams, was published in Nature Machine Intelligence, in collaboration with Professor Dhireesha Kudithipudi at the University of Texas at San Antonio, along with 22 other universities.
ABOUT PETER DIAMANDIS
Peter is the founder and executive chairman of the XPRIZE Foundation, and has started over 20 companies in the areas of longevity, space, venture capital and education. He is also the New York Times bestselling author of several books, including his latest, Life Force, which he published early in 2020 with Tony Robbins.
Peter joined host Robert Glazer on the Elevate Podcast to discuss transformational changes needed in education, how the pandemic accelerated global trends, and the astonishing medical and health technologies he believes will be widely available, sooner than you think.
The only way life extension would remain financially out of reach is if we vote ourselves into a dystopia.
Dr David Sinclair explains why aging therapies will be eventually affordable to us in this clip.
David Sinclair is a professor in the Department of Genetics and co-director of the Paul F. Glenn Center for the Biology of Aging at Harvard Medical School, where he and his colleagues study sirtuins—protein-modifying enzymes that respond to changing NAD+ levels and to caloric restriction—as well as chromatin, energy metabolism, mitochondria, learning and memory, neurodegeneration, cancer, and cellular reprogramming.
Dr David Sinclair has suggested that aging is a disease—and that we may soon have the tools to put it into remission—and he has called for greater international attention to the social, economic and political and benefits of a world in which billions of people can live much longer and much healthier lives.
Dr David Sinclair is the co-founder of several biotechnology companies (Life Biosciences, Sirtris, Genocea, Cohbar, MetroBiotech, ArcBio, Liberty Biosecurity) and is on the boards of several others.
After eating up about one billion base pairs to fuel its synthetic biology and cell programming efforts, Ginkgo Bioworks is going back for seconds, with another large order from the DNA weaver Twis | After eating up about one billion base pairs to fuel its synthetic biology and cell programming efforts, Ginkgo Bioworks is going back for seconds, with another large order from the DNA weaver Twist Bioscience.
Breakthrough techniques in living cells upend field.
Two studies provide a radically new picture of how bacterial cells continually repair damaged sections (lesions) in their DNA.
Led by researchers from NYU Grossman School of Medicine, the work revolves around the delicacy of DNA molecules, which are vulnerable to damage by reactive byproducts of cellular metabolism, toxins, and ultraviolet light. Given that damaged DNA can result in detrimental DNA code changes (mutations) and death, cells evolved to have DNA repair machineries. A major unresolved question in the field, however, is how do these machineries rapidly search for and find rare stretches of damage amid the “vast fields” of undamaged DNA.
Study shows that compound from cardamom shows promise for treating aggressive breast cancer.
Cardamonin — a natural compound found in the spice cardamom and other plants — could have therapeutic potential for triple-negative breast cancer, according to a new study using human cancer cells. The findings also show that the compound targets a gene that helps cancer cells elude the immune system.
About 10–15% of breast cancers are triple-negative, which means they don’t have receptors for estrogen or progesterone and don’t make excess amounts of a protein called HER2. These tumors are difficult to treat because they don’t respond to the hormone-based therapies used for other types of breast cancer. They also tend to be more aggressive and have a higher mortality rate than other breast cancers.