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Related Experiment Video

Updated: Jun 23, 2026

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
08:34

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies

Published on: February 6, 2019

Photon activation therapy and brachytherapy.

Brenda H Laster1, Dabney W Dixon, Sara Novick

  • 1Department of Nuclear Engineering, Ben Gurion University of the Negev, Beer Sheva, Israel. blaster@bgumail.bgu.ac.il

Brachytherapy
|May 12, 2009
PubMed
Summary
This summary is machine-generated.

Photon activation therapy (PAT) using platinum (Pt) and palladium-103 seeds slowed tumor growth in mice by inducing Auger electron emission. This targeted approach enhanced DNA damage for potential cancer treatment applications.

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Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
08:34

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05:39

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Published on: February 9, 2021

Area of Science:

  • Oncology
  • Medical Physics
  • Radiochemistry

Background:

  • Photon activation therapy (PAT) aims to enhance localized radiation dose in tumors.
  • High Z atoms complexed with DNA can amplify energy deposition via the photoelectric effect.
  • Auger electron emission, triggered by photoelectric effect, can cause significant local DNA damage.

Purpose of the Study:

  • To evaluate the efficacy of PAT in vivo.
  • To investigate the use of X-rays from palladium-103 seeds to excite platinum (Pt) atoms bound to DNA.
  • To assess the impact on cancerous cell DNA in murine models.

Main Methods:

  • Utilized Pt (II) tetrakis(N-methyl-4-pyridyl) porphyrin chloride to bind Pt atoms to DNA in KHJJ murine mammary carcinoma.
  • Implanted a 2.3-mCi palladium-103 seed directly into the tumor.
  • Monitored tumor growth rates in treated and control groups.

Main Results:

  • Tumor periphery received subtherapeutic radiation doses.
  • Mice treated with PAT exhibited a slower tumor growth rate compared to those receiving only brachytherapy.
  • Evidence suggests localized damage due to Auger electron emission from Pt atoms.

Conclusions:

  • Tumor growth delay in PAT-treated mice is likely due to Auger electron emission from Pt atoms, causing significant local DNA damage.
  • The study supports the hypothesis that PAT can enhance tumor cell killing.
  • Further research is needed to rule out other contributing mechanisms.