Theoretical strategy targets metabolic enzymes in tumors, suggesting improved detection and therapy precision.
The limitations of conventional cancer therapies, such as low selectivity and significant side effects, necessitate innovative approaches. This study proposes a pioneering self-theranostic strategy using magnesium-28 (Mg-28) alone, enabling simultaneous diagnosis, therapy, and treatment monitoring. Exploiting the elevated Mg ion demand in cancer cells, Mg-28 selectively targets Mg-dependent enzymes (e.g., DNA/RNA polymerases, hexokinase, telomerase) within intracellular organelles, such as the nucleus and mitochondria, without requiring biochemical carriers or nanoparticles, as in recent methods. A theoretical model based on the Mg-uptake coefficient predicts selective Mg-28 accumulation in tumors following intravenous administration. The Mg-28 decay chain—progressing through Aluminum-28 to stable Silicon-28—delivers highly localized irradiation through beta particles, Auger electrons, and recoil ions to critical intracellular structures, while simultaneously disrupting essential Mg-dependent enzymes. This results in a dual mechanism of radiotherapy and multi-enzyme inactivation. Simulations of linear energy transfer, radiation range, and absorbed dose show that nanogram-scale amounts of Mg-28 can deliver 60–400 Gy to tumors ranging from 0.03 mg to 500 g, suggesting potent cytotoxicity across a broad range of tumor sizes and stages. This potential is grounded in the universal metabolic reliance of cancer cells on Mg. Moreover, gamma emissions from Mg-28 and its daughter isotopes support early tumor detection and real-time treatment monitoring, enhancing therapeutic precision. As the first proposed single-isotope theranostic approach leveraging Mg dependency, this innovative strategy provides a robust foundation for future pre-clinical and clinical investigations aimed at validating its therapeutic efficacy, pharmacokinetics, and biosafety—thereby inaugurating a novel hypothesis for cancer therapy.
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Tran Van Luyen (2025) studied this question.
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