Breast cancer disrupts brain rhythms early in mice

Scientists at Cold Spring Harbor Laboratory have found that breast cancer quickly disrupts the brain's internal clock in mice, flattening daily stress hormone cycles and impairing immune responses. Remarkably, restoring these rhythms in specific brain neurons shrank tumors without any drugs. The discovery highlights how early physiological imbalances may worsen cancer outcomes.

Researchers led by Jeremy Borniger, an assistant professor at Cold Spring Harbor Laboratory, investigated how breast cancer affects the brain's regulation of stress and immunity. In mouse models, tumors interfered with diurnal rhythms—the natural day-night cycles of stress hormones. Normally, corticosterone levels in mice (equivalent to cortisol in humans) rise and fall predictably. However, breast tumors caused these levels to remain unnaturally flat, even before the tumors were detectable by touch.

This disruption emerged rapidly: within three days of cancer induction, the rhythm was blunted by 40 to 50 percent. Borniger noted, "Even before the tumors were palpable, we see about a 40 or 50% blunting of this corticosterone rhythm." The irregularity stems from the hypothalamic-pituitary-adrenal (HPA) axis, where hypothalamic neurons became hyperactive yet produced weak signals, throwing off the feedback loop that governs stress, sleep, and immune function.

Such imbalances are linked to common cancer symptoms like anxiety and insomnia, and in the mice, they correlated with reduced quality of life and higher mortality. The team then tested an intervention: stimulating these neurons to mimic normal day-night patterns. This reset normalized hormone cycles, prompting immune cells to infiltrate tumors and significantly reducing their size.

Borniger explained the timing's importance: "Enforcing this rhythm at the right time of day increased the immune system's ability to kill the cancer... If we do the same stimulation at the wrong time of day, it no longer has this effect." Notably, no anti-cancer drugs were used; the focus was on physiological health. The findings, published in Neuron in 2025, suggest enhancing body rhythms could complement treatments, potentially reducing therapy toxicity. Further research aims to uncover how tumors initially disrupt these cycles.

相关文章

Microscopic illustration of migrating neurons in the developing brain showing DNA damage and repair.
AI 生成的图像

Developing neurons sustain and rapidly repair DNA double-strand breaks during migration, study finds

由 AI 报道 AI 生成的图像 事实核查

A study in Nature reports that newborn neurons can incur double-strand DNA breaks while squeezing through tight spaces in the developing brain, and that healthy cells typically repair most of this damage within about a day.

Researchers have shown that stimulating specific brain activity in awake mice produces some of the restorative effects of deep sleep, including improved memory. The team now plans to explore whether a similar approach could work in people.

由 AI 报道

Researchers have identified a specific group of neurons in the amygdala that plays a central role in anxiety and social withdrawal. By restoring normal activity in this circuit, they reversed anxiety-related behaviors in mice. The findings point to a potential new target for treating emotional disorders.

Researchers at Boston Children’s Hospital report that mutations commonly associated with clonal blood-cell expansion and some blood cancers were enriched in microglia-like immune cells in Alzheimer’s brains and were also detectable in matched blood samples. The Cell study proposes that age- or injury-related weakening of the blood-brain barrier could allow mutated blood immune cells to enter the brain, potentially amplifying inflammation and contributing to neurodegeneration.

由 AI 报道

Scientists at McMaster University and the Hospital for Sick Children in Canada have discovered that oligodendrocytes, cells typically supporting nerve function, aid the growth of glioblastoma by sending signals to tumor cells. Blocking this communication slowed tumor progression in lab models. The findings suggest an existing HIV drug, Maraviroc, could be repurposed for treatment.

此网站使用 cookie

我们使用 cookie 进行分析以改进我们的网站。阅读我们的 隐私政策 以获取更多信息。
拒绝