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Breakthrough as two FDA-approved drugs are found to reverse Alzheimer's — including restoring memory
Breakthrough as two FDA-approved drugs are found to reverse Alzheimer's — including restoring memory

New York Post

time3 days ago

  • Health
  • New York Post

Breakthrough as two FDA-approved drugs are found to reverse Alzheimer's — including restoring memory

In a stunning scientific discovery, researchers have found that a pair of drugs can not only slow down Alzheimer's disease but actually reverse it and restore memory in mice. And the best part of all? Both are already FDA-approved — albeit for cancer. Researchers first pinpointed how Alzheimer's disease scrambles gene activity in individual brain cells. 3 Researchers have found that a pair of drugs can not only slow down Alzheimer's disease but actually reverse it and restore memory in mice. Pixel-Shot – Using the Connectivity Map database of 1,300 FDA‑approved drugs, the researchers looked for medications that reverse Alzheimer's‑associated gene expression — landing on a shortlist of five, and zeroing in on two cancer drugs. In what one researcher called a 'mock clinical trial,' they then mined 1.4 million patients' medical records, finding that those who had taken letrozole or irinotecan for cancer were significantly less likely to develop Alzheimer's. When given together in an aggressive Alzheimer's mouse model, letrozole — used to treat certain types of breast cancer in postmenopausal women — and irinotecan — an anti-cancer medication used to treat colon cancer and small cell lung cancer — reversed disease‑related gene expression signatures, dissolved toxic tau protein clumps and prevented brain degeneration. Most importantly, they restored memory and learning in mice that had already developed severe symptoms. It's an exciting development for an illness that's notoriously tricky. 3 Letrozole — used to treat certain types of breast cancer in postmenopausal women — and irinotecan — an anti-cancer medication used to treat colon cancer and small cell lung cancer — reversed disease‑related gene expression signatures, dissolved toxic tau protein clumps and prevented brain degeneration. Eric Hood – 'Alzheimer's disease comes with complex changes to the brain, which has made it tough to study and treat, but our computational tools opened up the possibility of tackling the complexity directly,' Marina Sirota, the interim director of the UCSF Bakar Computational Health Sciences Institute, said in a statement. 'We're excited that our computational approach led us to a potential combination therapy for Alzheimer's based on existing FDA-approved medications.' 'Alzheimer's is likely the result of numerous alterations in many genes and proteins that, together, disrupt brain health,' said Yadong Huang, a professor of neurology and pathology at UCSF. 'This makes it very challenging for drug development — which traditionally produces one drug for a single gene or protein that drives disease.' 3 'Alzheimer's is likely the result of numerous alterations in many genes and proteins that, together, disrupt brain health,' said Yadong Huang, a professor of neurology and pathology at UCSF. yurakrasil – The findings were published in the journal Cell. Both drugs are already FDA‑approved for other uses, which could dramatically speed up the path to human trials. However, because they are cancer drugs, repurposing them may be complex and risky. This finding adds to a growing number of potential Alzheimer's treatments. A compound found in rosemary and sage — carnosic acid — has been shown to reverse memory loss and reduce brain inflammation in mice with Alzheimer's, bringing their cognitive function back to near-normal levels. A study from Stanford Medicine found that seniors who received the shingles vaccine were 20% less likely to develop dementia over seven years. And researchers at Penn State and Stanford University discovered that a certain cancer drug could restore memory and brain function in early stage Alzheimer's models.

Alzheimer: Researchers find two cancer drugs reverse damaged gene behaviour in mice
Alzheimer: Researchers find two cancer drugs reverse damaged gene behaviour in mice

Time of India

time23-07-2025

  • Health
  • Time of India

Alzheimer: Researchers find two cancer drugs reverse damaged gene behaviour in mice

New Delhi: A study that compared gene behaviour in Alzheimer's disease with that caused by 1,300 drugs approved for use in the US has found that a combination of two cancer drugs could slow the neurodegenerative disease in mice, indicating a promise in reversing symptoms in humans. Alzheimer's disease is an ageing-related disorder in which cognitive function steadily declines, affecting speech and memory, and eventually can interfere with everyday activities. Scientists at the University of California, San Francisco, and Gladstone Institutes in the US first saw how gene behaviour was affected in Alzheimer's disease in a single brain cell. The researchers then looked at 1,300 drugs approved by the US Food and Drug Administration (FDA) and which of them reversed the damage. The next stage of the study, published in the journal 'Cell', analysed electronic medical records of about 1.4 million patients and found that patients who took some of these drugs for treating conditions other than Alzheimer's disease were less likely to get the ageing-related neurological disorder. Testing the top two drug candidates -- ' letrozole ' and ' irinotecan ', both of which are cancer medications -- in a mouse model having Alzheimer's disease, the researchers found that brain degeneration was reduced and a restored ability to remember. Letrozole is usually prescribed for treating breast cancer, and irinotecan for colon and lung cancer. The combined effects of two drugs were found to reverse damaged gene behaviour in neurons and glia (a type of brain cells that surround and support neurons). Further, toxic clumps of proteins and brain degeneration -- hallmark features of Alzheimer's -- were found to be reduced and memory restored, the researchers said. The team added that out of 1,300 drugs, 86 reversed gene behaviour changes in one type of brain cell and 25 reversed them in other types. However, only 10 had been approved for use in humans by the FDA. "Thanks to all these existing data sources, we went from 1,300 drugs, to 86, to 10, to just five," said lead author Yaqiao Li, a postdoctoral scholar at Gladstone Institutes. "Alzheimer's disease comes with complex changes to the brain which has made it tough to study and treat, but our computational tools opened up the possibility of tackling the complexity directly," said co-senior author Marina Sirota, professor of paediatrics and an interim director at the University of California. Co-senior author Yadong Huang, director of the center for translational advancement at Gladstone Institutes, said, "Alzheimer's is likely the result of numerous alterations in many genes and proteins that, together, disrupt brain health." "This makes it very challenging for drug development -- which traditionally produces one drug for a single gene or protein that drives disease," Huang said. The electronic medical records analysed in the study came from the University of California's Health Data Warehouse, which includes anonymised health information on 1.4 million people over the age of 65.

Alzheimer's disease: Researchers find two cancer drugs reverse damaged gene behaviour in mice
Alzheimer's disease: Researchers find two cancer drugs reverse damaged gene behaviour in mice

The Hindu

time22-07-2025

  • Health
  • The Hindu

Alzheimer's disease: Researchers find two cancer drugs reverse damaged gene behaviour in mice

A study that compared gene behaviour in Alzheimer's disease with that caused by 1,300 drugs approved for use in the US has found that a combination of two cancer drugs could slow the neurodegenerative disease in mice, indicating a promise in reversing symptoms in humans. Alzheimer's disease is an ageing-related disorder in which cognitive function steadily declines, affecting speech and memory, and eventually can interfere with everyday activities. Scientists at the University of California, San Francisco, and Gladstone Institutes in the US first saw how gene behaviour was affected in Alzheimer's disease in a single brain cell. The researchers then looked at 1,300 drugs approved by the US Food and Drug Administration (FDA) and which of them reversed the damage. The next stage of the study, published in the journal 'Cell', analysed electronic medical records of about 1.4 million patients and found that patients who took some of these drugs for treating conditions other than Alzheimer's disease were less likely to get the ageing-related neurological disorder. Testing the top two drug candidates -- 'letrozole' and 'irinotecan', both of which are cancer medications -- in a mouse model having Alzheimer's disease, the researchers found that brain degeneration was reduced and a restored ability to remember. Letrozole is usually prescribed for treating breast cancer, and irinotecan for colon and lung cancer. The combined effects of two drugs were found to reverse damaged gene behaviour in neurons and glia (a type of brain cells that surround and support neurons). Further, toxic clumps of proteins and brain degeneration -- hallmark features of Alzheimer's -- were found to be reduced and memory restored, the researchers said. The team added that out of 1,300 drugs, 86 reversed gene behaviour changes in one type of brain cell and 25 reversed them in other types. However, only 10 had been approved for use in humans by the FDA. "Thanks to all these existing data sources, we went from 1,300 drugs, to 86, to 10, to just five," said lead author Yaqiao Li, a postdoctoral scholar at Gladstone Institutes. "Alzheimer's disease comes with complex changes to the brain which has made it tough to study and treat, but our computational tools opened up the possibility of tackling the complexity directly," said co-senior author Marina Sirota, professor of paediatrics and an interim director at the University of California. Co-senior author Yadong Huang, director of the center for translational advancement at Gladstone Institutes, said, "Alzheimer's is likely the result of numerous alterations in many genes and proteins that, together, disrupt brain health." "This makes it very challenging for drug development -- which traditionally produces one drug for a single gene or protein that drives disease," Huang said. The electronic medical records analysed in the study came from the University of California's Health Data Warehouse, which includes anonymised health information on 1.4 million people over the age of 65.

Two NHS drugs slows and could REVERSE devastating Alzheimer's, ‘exciting' study finds
Two NHS drugs slows and could REVERSE devastating Alzheimer's, ‘exciting' study finds

Scottish Sun

time21-07-2025

  • Health
  • Scottish Sun

Two NHS drugs slows and could REVERSE devastating Alzheimer's, ‘exciting' study finds

Click to share on X/Twitter (Opens in new window) Click to share on Facebook (Opens in new window) TWO NHS drugs could be combined to treat, and even reverse, the most common form of dementia, scientists claim. A pair of cancer drugs have been identified as a powerful duo that may tackle Alzheimer's disease, after scientists sifted through 1,300 approved medicines. Sign up for Scottish Sun newsletter Sign up 1 Alzheimer's was reversed in mice Credit: Alamy The American team used cutting-edge computer tools to match the gene changes seen in Alzheimer's patients with medicines that reverse those effects. They found that two cancer drugs, both already available on the NHS, reduced brain degeneration in mice with the disease, and even brought back their memory. The study, from the University of California, San Francisco (UCSF), first looked at how Alzheimer's alters the activity of individual brain cells. They then searched for existing drugs that trigger the opposite changes, with the aim of rewiring damaged neurons and brain cells called glia. And when they tested the top two candidates, letrozole and irinotecan, in lab mice, the results were impressive. One theory of how Alzheimer's comes about is that sticky proteins - like amyloid-beta - start clumping together in the brain years before symptoms appear. These toxic clumps block communication between brain cells and trigger inflammation, eventually causing the cells to die. Some scientists believe this buildup is the root cause of Alzheimer's, so clearing it could stop the disease in its tracks. When combined, the cancer drugs not only halted brain cell damage but also undid toxic clumps of proteins, restored memory and reversed the disease's genetic footprint. Prof Marina Sirota, senior author, said: 'We're excited that our computational approach led us to a potential combination therapy for Alzheimer's based on existing FDA-approved medications.' Common painkiller used for back pain ups risk of dementia by 29%, scientists warn She added: 'Alzheimer's disease comes with complex changes to the brain, which has made it tough to study and treat — but our tools opened up the possibility of tackling that complexity directly.' The scientists then trawled through the anonymised medical records of 1.4million over-65s and found those already taking the cancer drugs were less likely to develop Alzheimer's. Dr Yaqiao Li, the study's lead author, said: 'Thanks to all these existing data sources, we went from 1,300 drugs, to 86, to 10, to just five. 'In particular, the rich data collected by all the UC health centres pointed us straight to the most promising drugs. It's kind of like a mock clinical trial.' Letrozole is typically used to treat breast cancer, while irinotecan is prescribed for colon and lung cancer. Both are already used in the UK. 'So exciting' Prof Yadong Huang, co-senior author, said: 'Alzheimer's is likely the result of numerous alterations in many genes and proteins that, together, disrupt brain health. 'This makes it very challenging for drug development - which traditionally produces one drug for a single gene or protein that drives disease.' He added: 'It's so exciting to see the validation of the computational data in a widely used Alzheimer's mouse model.' The breakthrough, published in the journal Cell, could fast-track trials in humans. Prof Sirota said: 'If completely independent data sources, such as single-cell expression data and clinical records, guide us to the same pathways and the same drugs and then resolve Alzheimer's in a genetic model then maybe we're onto something.' She added: 'We're hopeful this can be swiftly translated into a real solution for millions of patients with Alzheimer's.' Alzheimer's causes a relentless decline in cognition, learning, and memory. But decades of research have only produced two FDA-approved drugs, neither of which can meaningfully slow the decline. In the UK, no disease-modifying drugs are currently approved or available. Instead, the UK relies on symptom-managing drugs, such as Donepezil and Rivastigmine.

Gen Zer Reaches Final Stage of Chemo—Has No Idea Devastating News Is Coming
Gen Zer Reaches Final Stage of Chemo—Has No Idea Devastating News Is Coming

Newsweek

time22-06-2025

  • Health
  • Newsweek

Gen Zer Reaches Final Stage of Chemo—Has No Idea Devastating News Is Coming

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. When Alexis Klimpl discovered a grape-sized lump in her breast, her gut immediately told her it was cancer. But due to her young age, she tried to convince herself it couldn't be. However, a series of tests and scans confirmed the worst: she had stage 2 triple-positive breast cancer at just 24 years old. Now, one year later, the publicist from San Diego, California, is in remission. But she's also navigating early menopause brought on by her treatment. "I can't have kids for 10 more years because of the medication I'm on," she told Newsweek. Klimpl takes Lupron, a drug used to reduce the risk of hormone-receptor-positive breast cancer returning in premenopausal women following surgery and other treatments. She also takes Letrozole, a hormone blocker. "I never thought I'd be in menopause at 25," she said. "I have 10 to 15 hot flashes a day, night sweats, ongoing hair loss, vaginal dryness and mood swings." Most women begin the menopausal transition between the ages of 45 and 55, with symptoms often lasting for several years. Breast cancer, too, is typically associated with older women—the American Cancer Society reports that the median age at diagnosis is 62. Although uncommon, a small percentage of cases do occur in women under 45. L-R: Klimpl with her partner and Klimpl sitting in the hospital during cancer treatment. L-R: Klimpl with her partner and Klimpl sitting in the hospital during cancer treatment. Alexis Klimpl Dr. Mary Jane Minkin, the co-director of the sexuality, intimacy and menopause for cancer survivors program at Smilow Cancer Hospital in New Haven, Connecticut, explained to Newsweek why patients like Klimpl go through a medicated menopause. "The problem here is that for a woman who has (presumed) estrogen receptor positive breast cancer, all oncologists would want to avoid giving her estrogen, and indeed would probably give her medications to minimize her own body's production of any estrogen from any non-ovarian source," Minkin said. With no family history of breast cancer, Klimpl and her mother were devastated by the diagnosis. "I thought I was too young to have cancer," she told Newsweek, explaining that she initially hoped it was just a cyst, but she could feel it growing. "When I was diagnosed, the doctors didn't know how it happened. They said it's rare at my age. My mom broke down. Seeing her face—I'll never forget that image," Klimpl said. A friend set up a GoFundMe page for Klimpl that raised $23,000. Half of the funds went toward egg freezing, during which 36 eggs were retrieved. The rest helped cover the costs of six surgeries, each priced at $3,000. L-R: Klimpl flashing a peace sign and with her mother during a hospitalization. L-R: Klimpl flashing a peace sign and with her mother during a hospitalization. Alexis Klimpl/Alexis Klimpl Klimpl underwent six rounds of chemotherapy over the course of nearly five months and was officially declared cancer-free in January of this year. Despite genetic tests showing no inherited cancer risk, she chose to have a double mastectomy. "In my eyes, my breasts betrayed me. They didn't have my back, so I wanted them gone," she said. Klimpl has since undergone breast reconstruction, which she lightheartedly refers to on Instagram (@lexiklimpl) as "the only positive" of her cancer experience. Reflecting on the past year, she told Newsweek: "As a young person, you feel invincible—but being diagnosed at such a young age really put my life into perspective." "It strengthened my relationships with friends and family because they showed up for me in ways I'll never forget. I've realized that we often don't know how to be there for others when we're just trying to keep ourselves together," she said. "I'm finally at a stage where it feels like everything is behind me. I'm returning to my life—but it's strange. I thought that hearing the words 'cancer-free' would bring instant relief, that it would be the moment the stress disappeared. But it wasn't. Recovery is more complex than I expected."

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