Δευτέρα 10 Φεβρουαρίου 2020

Protons show greater relative biological effectiveness for mammary tumorigenesis with higher ERα and HER2 positive tumors relative to γ-rays in APCMin/+ mice.

Protons show greater relative biological effectiveness for mammary tumorigenesis with higher ERα and HER2 positive tumors relative to γ-rays in APCMin/+ mice.:

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Protons show greater relative biological effectiveness for mammary tumorigenesis with higher ERα and HER2 positive tumors relative to γ-rays in APCMin/+ mice.

Int J Radiat Oncol Biol Phys. 2020 Feb 06;:

Authors: Suman S, Shuryak I, Kallakury B, Brenner DJ, Fornace AJ, Johnson MD, Datta K

Abstract

PURPOSE: Exposure to ionizing radiation increases risk of breast cancer. Although proton radiation is encountered in outer space and in medicine, we do not fully understand breast cancer risks from protons due to limited in vivo data. The purpose of this study was to comparatively assess the effects of γ-rays and protons on mammary tumorigenesis in APCMin/+ mice.

METHODS AND MATERIALS: Female APCMin/+ mice were exposed to 1 GeV protons (1.88 or 4.71 Gy) and 137Cs γ-rays (2 or 5 Gy). Mice were euthanized 100 to 110 days after irradiation, mammary tumors scored, tumor grades assessed, and relative biological effectiveness (RBE) calculated. Molecular phenotypes were determined by assessing estrogen receptor α (ERα) and human epidermal growth factor receptor 2 (HER2) status. ERα downstream signaling was assessed by immunohistochemistry.

RESULTS: Exposure to proton radiation led to increased mammary tumor frequency at both proton radiation doses compared to γ-rays. The calculated RBE for proton radiation-induced mammary tumorigenesis was 3.11 for all tumors and >5 for malignant tumors relative to γ-rays. Tumor frequency per unit of radiation was higher at the lower dose suggesting a saturation effect at the higher dose. Protons induced more adenocarcinomas relative to γ-rays, and proton-induced tumors show greater ERα and HER2 positivity and higher activation of the ERα-downstream PI3K/Akt and cyclin D1 pathways relative to γ-rays.

CONCLUSIONS: Our data demonstrate that protons pose a higher risk of mammary tumorigenesis relative to γ-rays. We also show that proton radiation-induced tumors in APCMin/+ mice are ERα and HER2 positive, which is consistent with our previous data on radiation-induced estrogenic response in wild-type mice. While this study establishes APCMin/+ as a model with adequate signal-to-noise ratio for space radiation-induced mammary tumorigenesis, further studies will be required for addressing the uncertainties in space radiation-induced breast cancer risk estimation.

PMID: 32036005 [PubMed - as supplied by publisher]

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