Scientists at Northwestern University lab observing nanotherapy targeting leukemia cells in mice, illustrating cancer treatment breakthrough.
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Northwestern nanotherapy supercharges 5-fluorouracil and spares healthy cells in leukemia mice

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A Northwestern University team reports that redesigning the chemotherapy drug 5‑fluorouracil as a spherical nucleic acid markedly increased its cancer‑cell uptake and efficacy in acute myeloid leukemia models, with no observable side effects, according to a study published October 29 in ACS Nano.

Northwestern University scientists re‑engineered 5‑fluorouracil (5‑Fu) into a spherical nucleic acid (SNA) — DNA strands densely arranged around a nanoscale core with the drug built into the strands — and tested it against acute myeloid leukemia (AML) in mice. The work, led by Chad A. Mirkin, was published online October 29 in ACS Nano. (news.northwestern.edu)

In cell and animal studies, the SNA version entered leukemia cells 12.5 times more efficiently than standard 5‑Fu and achieved a 59‑fold improvement in antitumor efficacy in a human AML mouse model, with no observable side effects reported. The PubMed record for the paper describes “up to four orders of magnitude” (i.e., up to 10,000‑fold) enhancement in in‑vitro cell killing versus free 5‑Fu; Northwestern’s news materials state killing was “up to 20,000 times” more effective. Taken together, the peer‑reviewed abstract supports at least a 10,000‑fold in‑vitro gain, while university communications cite a higher figure. (pubmed.ncbi.nlm.nih.gov)

The approach aims to solve a long‑standing limitation of 5‑Fu: poor solubility. Less than 1% dissolves in many biological fluids, which hampers absorption and contributes to toxicity from high dosing, Northwestern notes. By integrating the drug into the SNA’s DNA shell, the construct leverages cell‑surface scavenger receptors that myeloid cells overexpress, enabling preferential uptake by AML cells and sparing healthy tissue in the reported mouse experiments. (news.northwestern.edu)

“In animal models, we demonstrated that we can stop tumors in their tracks,” Mirkin said, adding that the goal is more effective chemotherapy with fewer side effects. The study’s next steps include larger cohorts of small animals, progression to a large‑animal model, and, contingent on funding, eventual human trials. (news.northwestern.edu)

Northwestern frames the work within “structural nanomedicine,” in which a therapy’s architecture is tuned to control how it behaves in the body. The university says seven SNA‑based therapies are already in human clinical trials, underscoring the platform’s translational momentum even as the 5‑Fu SNA remains at the preclinical stage. (news.northwestern.edu)

Makala yanayohusiana

Scientific illustration depicting nasal nanodrops activating immune cells to eliminate glioblastoma tumors in a mouse model.
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Nasal nanodrops wipe out glioblastoma tumors in mice

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Researchers at Washington University School of Medicine in St. Louis, working with scientists at Northwestern University, have developed a noninvasive nasal nanotherapy that activates the immune system to attack aggressive brain tumors in mice. By delivering spherical nucleic acids that trigger the STING immune pathway directly from the nose to the brain, the approach eliminated glioblastoma tumors in mouse models when combined with drugs that boost T-cell activity, according to a study in the Proceedings of the National Academy of Sciences.

Scientists at Northwestern Medicine have developed an antibody that counters pancreatic cancer's sugar-based disguise, enabling the immune system to attack tumors more effectively. In mouse studies, the therapy slowed tumor growth by restoring immune activity. The team is preparing the antibody for human trials.

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Scientists at RMIT University have created tiny molybdenum oxide nanodots that destroy cancer cells by amplifying their internal stress, while leaving healthy cells largely intact. In lab tests, these particles proved three times more effective against cervical cancer cells than healthy ones. The early-stage research points to a potential for more precise cancer treatments.

A small study from researchers in India has found that a short course of an oral combination of resveratrol and copper was associated with reduced biological markers of aggressiveness in glioblastoma tumors, without reported side effects. Patients who took the nutraceutical before surgery showed lower levels of several key cancer-related markers in their tumor samples, and the approach targets harmful DNA-containing particles released from dying cancer cells.

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Researchers at KAIST have developed an injection that transforms immune cells within tumors into active cancer-killing agents, bypassing the need for complex lab procedures. The method uses lipid nanoparticles to deliver instructions directly to macrophages, enabling them to recognize and attack cancer cells while boosting broader immune responses. In animal tests, the approach significantly slowed tumor growth in melanoma models.

Scientists have identified a genetic modifier that helps cells cope with the loss of frataxin, the protein at the core of Friedreich’s ataxia. By lowering activity of the FDX2 gene, experiments in worms, human cells, and mice showed that key energy‑producing processes can be restored, pointing to a potential new treatment strategy.

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Researchers from MIT and Stanford University have developed multifunctional molecules called AbLecs to block sugar-based immune checkpoints on cancer cells. This approach aims to enhance immunotherapy by allowing immune cells to better target tumors. Early tests in cells and mice show promising results in boosting anti-tumor responses.

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