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Blocking NONO Molecules Enhances Immune Response Against Aggressive Breast Cancer

Blocking NONO Molecules Enhances Immune Response Against Aggressive Breast Cancer

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New research identifies NONO protein as a key player in breast cancer immune evasion. Inhibition of NONO triggers immune response, paving the way for innovative therapies against triple-negative breast cancer.

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Recent research has uncovered a promising new target in the fight against triple-negative breast cancer, one of the most aggressive and treatment-resistant forms of the disease. Conducted by Italy’s National Cancer Institute Pascale Foundation’s Senology Department in collaboration with the Sbarro Institute for Cancer Research and Molecular Medicine in Philadelphia, the study reveals that the protein NONO plays a critical role in suppressing the immune system’s natural defenses in cancer cells.

The study, published in the International Journal of Molecular Sciences, explains that NONO is produced in abnormally high levels in triple-negative breast cancer cells, contributing to the tumor's ability to evade immune detection. Researchers found that reducing NONO levels—either through specialized gene-silencing techniques like siRNA or with chemical inhibitors—can trigger an immune response, potentially restoring the body's capacity to fight the tumor.

This discovery offers a new avenue for therapy, suggesting that inhibiting NONO could make cancer cells more vulnerable to immune attacks. The idea is to combine NONO inhibitors with existing immune checkpoint modulators, drugs already used successfully in other cancer treatments, to develop more effective therapeutic strategies.

The research team, led by Michelino De Laurentiis, emphasized that while these results are preliminary, they highlight a promising direction for developing additional treatments for triple-negative breast cancer, which currently has limited options. The collaborative effort also involved longstanding partnerships, including Professor Antonio Giordano from Temple University, facilitating ongoing research into breast cancer mechanisms.

This groundbreaking insight shifts focus toward targeting cellular proteins that regulate immune suppression in cancer, opening doors for future therapies that enhance the body's innate ability to combat aggressive tumors.

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