Lifeboat Foundation

Two groundbreaking studies recently published in the journals Nature and Genome Medicine found genetic signatures that explain ethnic disparities in the severity of prostate cancer, notably in Sub-Saharan Africa.

By genetically analyzing prostate cancer tumors from Australian, Brazilian, and South African donors, the team developed a new prostate cancer taxonomy (classification scheme) and cancer drivers that not only distinguish patients based on their genetic ancestry but also predict which cancers are likely to become life-threatening, a task that is currently difficult.

“Our understanding of prostate cancer has been severely limited by a research focus on Western populations,” said senior author Professor Vanessa Hayes, genomicist and Petre Chair of Prostate Cancer Research at the University of Sydney’s Charles Perkins Centre and Faculty of Medicine and Health in Australia. “Being of African descent, or from Africa, more than doubles a man’s risk for lethal prostate cancer. While genomics holds a critical key to unraveling contributing genetic and non-genetic factors, data for Africa has till now, been lacking.”

Thanks to new RNA vaccines, we humans have been able to protect ourselves incredibly quickly from new viruses like SARS-CoV-2, the virus that causes COVID-19. These vaccines insert a piece of ephemeral genetic material into the body’s cells, which then read its code and churn out a specific protein—in this case, telltale “spikes” that stud the outside of the coronavirus—priming the immune system to fight future invaders.

The technique is effective, and has promise for all sorts of therapies, says Eerik Kaseniit, Ph.D. student in bioengineering at Stanford. At the moment, though, these sorts of RNA therapies can’t focus on specific cells. Once injected into the body, they indiscriminately make the encoded protein in every cell they enter. If you want to use them to treat only one kind of cell—like those inside a cancerous tumor—you’ll need something more precise.

Kaseniit and his advisor, assistant professor of chemical engineering Xiaojing Gao, may have found a way to make this possible. They’ve created a new tool called an RNA “sensor”—a strand of lab-made RNA that reveals its contents only when it enters particular tissues within the body. The method is so exact that it can home in on both cell types and cell states, activating only when its target cell is creating a certain RNA, says Gao. The pair published their findings Oct. 5 in the journal Nature Biotechnology.

Changing the epigenetic marks on chromosomes results in altered gene expression in offspring and in grandoffspring, demonstrating ‘transgenerational epigenetic inheritance.’

Without changing the genetic code in the DNA

DNA, or deoxyribonucleic acid, is a molecule composed of two long strands of nucleotides that coil around each other to form a double helix. It is the hereditary material in humans and almost all other organisms that carries genetic instructions for development, functioning, growth, and reproduction. Nearly every cell in a person’s body has the same DNA. Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA).

Understanding how metastasis works.

In the universal fight against cancer, metastasis is one of the most unpleasant factors that could make matters even worse; and there is still much to comprehend in the spread process. Cambridge scientists might have unveiled a breakthrough in understanding how metastasis works.

The research has been published in the journal Nature Genetics.

Continue reading “A breakthrough in metastasis could lead to better cancer treatments” »

A new study from the Garvan Institute of Medical Research shows how rises in core body temperature may trigger the inflammatory flares in people with a rare genetic autoinflammatory disease.

The recessive disorder, called mevalonate kinase deficiency (MKD), is caused by mutations in the gene for mevalonate kinase, an essential enzyme present in all cells in the body. Lack of this enzyme leads to a build-up of abnormal proteins, which causes cells of the immune system to malfunction and trigger inflammation.

Continue reading “Higher body temperature alters key protein in autoinflammatory disorder” »

Since the infancy of functional magnetic resonance imaging (fMRI) in 1990, people have been fascinated by the potential for brain scans to unlock the mysteries of the human mind, our behaviors and beliefs. Many breathtaking applications for brain scans have been devised, but hype often exceeds what empirical science can deliver. It’s time to ask: What’s the big picture of neuroscience and what are the limitations of brain scans?

The specific aims of any research endeavor depend on who you ask and what funding agency is involved, says Michael Spezio, associate professor of psychology, data science and neuroscience at Scripps College. Some people believe neuroscience has the potential to explain human cognition and behavior as a fully mechanistic process, ultimately debunking an “illusion of free will.” Not all neuroscientists agree that free will is a myth, but it’s a strong current these days. Neuroscience also has applications in finance, artificial intelligence, weapons research and national security.

For other researchers and funders, the specific aim of neuroscience involves focusing on medical imaging, genetics, the study of proteins (proteomics) and the study of neural connections (connectomics). As caring persons who are biological, neurological, physical, social and spiritual, we can use neuroscience to think carefully and understand our humanity and possible ways to escape some of the traps we’ve built for ourselves, says Spezio. Also, brain scans can enhance research into spirituality, mindfulness and theory of mind – the awareness of emotions, values, empathy, beliefs, intentions and mental states to explain or predict others’ behavior.

BGI Genomics, in collaboration with Southwest University, the State Key Laboratory of Silkworm Genome Biology, and other partners, has constructed a high-resolution pangenome dataset representing almost the entire genomic content in a silkworm.

This research paper, providing genetic insights into artificial selection (domestication and breeding) and ecological adaptation, was published on September 24 in Nature Communications.

Previously, due to the scarcity of wild silkworms and technical limitations of former studies, many trait-associated sites were missing. This is the first research ever to digitize silkworm gene pool and create a “digital silkworm”, greatly facilitating functional genomic research, promoting precise breeding, and thus enabling additional silk use cases.

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Bristle Discount Link (Oral microbiome quantification):
ConquerAging15
https://www.bmq30trk.com/4FL3LK/GTSC3/

Continue reading “Biohacking The Oral Microbiome: Test #2” »

Excerpt from an episode of Longevity by Design, hosted by Dr. Gil Blander and Ashley Reaver, MS, RD, CSSD, who were joined by Dr. George Church, Professor of Genetics at Harvard Medical School.

To watch the entire conversation clic here: https://youtu.be/6XnXeVS1m2U