4.7 Article

Targeted Alpha Therapy of Glioma Using 211At-Labeled Heterodimeric Peptide Targeting Both VEGFR and Integrins

Journal

MOLECULAR PHARMACEUTICS
Volume 19, Issue 9, Pages 3206-3216

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.2c00349

Keywords

astatine-211; heterodimeric peptide; cytotoxicity; targeted therapy

Funding

  1. National Natural Science Foundation of China [22006105]
  2. China Postdoctoral Science Foundation [2020M683309]
  3. Program of the Local Science and Technology Development (Gansu province) Guided by Central Government [GSCK20215111]
  4. Fundamental Research Funds for the Central Universities
  5. Sichuan University Postdoctoral Interdisciplinary Innovation Fund

Ask authors/readers for more resources

Targeted radionuclide therapy based on alpha-emitters is important in cancer treatment. This study proposes a new vector for At-211 radiolabeling and demonstrates its effectiveness in inhibiting tumor growth and promoting cell apoptosis without significant toxicity to normal organs.
Targeted radionuclide therapy based on alpha-emitters plays an increasingly important role in cancer treatment. In this study, we proposed to apply a heterodimeric peptide (iRGD-C6-lys-C6-DA7R) targeting both VEGFR and integrins as a new vector for At-211 radiolabeling to obtain highperformance radiopharmaceuticals with potential in targeted alpha therapy (TAT). An astatinated peptide, iRGD-C6-lys(At-211-ATE)-C6-DA7R, was prepared with a radiochemical yield of & SIM;45% and high radiochemical purity of > 95% via an electrophilic radioastatodestannylation reaction. iRGD-C6lys(211At-ATE)-C6-DA7R showed good stability in vitro and high binding ability to U87MG (glioma) cells. Systematic in vitro antitumor investigations involving cytotoxicity, apoptosis, distribution of the cell cycle, and reactive oxygen species (ROS) clearly demonstrated that At-211-labeled heterodimeric peptides could significantly inhibit cell viability, induce cell apoptosis, arrest the cell cycle in G2/M phase, and increase intracellular ROS levels in a dose-dependent manner. Biodistribution revealed that iRGDC6-lys(At-211-ATE)-C6-DA7R had rapid tumor accumulation and fast normal tissue/organ clearance, which was mainly excreted through the kidneys. Moreover, in vivo therapeutic evaluation indicated that iRGD-C6-lys(At-211-ATE)-C6-DA7R was able to obviously inhibit tumor growth and prolong the survival of mice bearing glioma xenografts without notable toxicity to normal organs. All these results suggest that TAT mediated by iRGD-C6-lys(At-211-ATE)-C6-DA7R can provide an effective and promising strategy for the treatment of glioma and some other tumors.

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