| Feb 09, 2024 |
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(Nanowerk News) A multidisciplinary research team at Vanderbilt University and Vanderbilt University Medical Center has discovered a new way to kill a tumor by disrupting its acidic “microenvironment” without harming normal tissue.
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The target of this unorthodox approach is hydroxyapatite (HAP), a naturally occurring mineral that is a major component of bone and teeth, but which also is produced by some tumors.
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In the extracellular microenvironment that surrounds and nourishes tumors, HAP crystals can enhance tumor cell proliferation, progression and migration (metastasis). However, HAP is absent in normal soft tissue, making it an attractive target for cancer imaging and treatment.
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| From left, images of a mouse model of breast cancer before and after NSPS administration. (Image: Vanderbilt University)
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Using various molecular analytical methods, the researchers identified and synthesized a nanoparticle that, when delivered via an injectable solution called NSPS, chelated, or bound to calcium on tumor-associated HAP crystals, causing them to dissolve.
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Dissolution triggered localized alkalosis, a sudden reversal in the acidity of the tumor microenvironment that was strong enough to kill breast cancer cells grown in culture, and to slow tumor growth in animal models of human breast, colon, lung and prostate cancers.
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At the same time, NSPS demonstrated limited interaction with normal soft tissue and bone, the researchers reported in the journal Cancer Medicine (“Tumor therapy by targeting extracellular hydroxyapatite using novel drugs: A paradigm shift”). These findings suggest that NSPS may be, in their words, “a one-of-a-kind and first in a class of novel cancer therapeutics.”
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The paper’s corresponding author, Mohammed Tantawy, PhD, MBA, is a research associate professor of Radiology & Radiological Sciences and a member of the Vanderbilt University Institute of Imaging Science at VUMC.
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The microenvironment of tumors generally is more acidic than surrounding normal tissue. Acidity, by altering the structure or uptake of cancer drugs, may contribute to the resistance to chemotherapy exhibited by tumors such as triple negative breast cancer, which has a high rate of recurrence and poor overall survival.
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“There is an urgent clinical need for new treatment paradigms that could improve the outcome for cancer patients with poor prognosis,” the researchers noted. While further studies in humans are necessary, “NSPS has significant potential to be a paradigm-changing approach to the treatment of cancer patients with poor prognosis.”
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Tantawy added: “Within the Institute of Imaging Science, we are fortunate to be able to take projects like this from initial conception through the development of novel ligands for detection and treatment of cancer into in vivo demonstrations based on multimodal imaging and even into human subjects.”
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