Cited by 29Effects of Radiation ExposureRadiation Therapy and DosimetryCancer-related Molecular Pathways

Densely Ionizing Radiation Acts via the Microenvironment to Promote Aggressive Trp53 -Null Mammary Carcinomas

Illa-Bochaca, Irineu, Ouyang, Haoxu, Tang, Jonathan, Sebastiano, Christopher, Mao, Jian-Hua, Costes, Sylvain V., Demaria, Sandra, Barcellos-Hoff, Mary Helen·2014·Cancer Research

Published version of a preprint

Abstract

Densely ionizing radiation, which is present in the space radiation environment and used in radiation oncology, has potentially greater carcinogenic effect compared with sparsely ionizing radiation that is prevalent on earth. Here, we used a radiation chimera in which mice were exposed to densely ionizing 350 MeV/amu Si-particles, γ-radiation, or sham-irradiated and transplanted 3 days later with syngeneic Trp53-null mammary fragments. Trp53-null tumors arising in mice irradiated with Si-particles had a shorter median time to appearance and grew faster once detected compared with those in sham-irradiated or γ-irradiated mice. Tumors were further classified by markers keratin 8/18 (K18, KRT18), keratin 14 (K14, KRT14) and estrogen receptor (ER, ESR1), and expression profiling. Most tumors arising in sham-irradiated hosts were comprised of both K18- and K14-positive cells (K14/18) while those tumors arising in irradiated hosts were mostly K18. Keratin staining was significantly associated with ER status: K14/18 tumors were predominantly ER-positive, whereas K18 tumors were predominantly ER-negative. Genes differentially expressed in K18 tumors compared with K14/18 tumor were associated with ERBB2 and KRAS, metastasis, and loss of E-cadherin. Consistent with this, K18 tumors tended to grow faster and be more metastatic than K14/18 tumors, however, K18 tumors in particle-irradiated mice grew significantly larger and were more metastatic compared with sham-irradiated mice. An expr…

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Crossref · 10.1158/0008-5472.can-14-1212

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1 of 1 references verified0 citation errors · 0 not checkable

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  • In mammary tumors, differences in tumor types comparing heavy ions to low LET radiation were observed, with more aggressive tumors observed.

    “Mammary tumors (Illa-Bochaca et al., 2014;Omene et al., 2020;Imaoka et al., 2007) Differences in mammary tumor types comparing heavy ions to low LET radiation with more aggressive tumors observed.”
  • NTEs have been shown to impact initiation, promotion and progression stages of tumorigenesis at low doses of high LET radiation.

    “NTE have been shown to impact initiation, promotion and progression stages of tumorigenesis at low doses of high LET radiation (Illa-Bochaca et al., 2014;Omene et al., 2020;Maxwell et al., 2008;Kadhim et al., 2013;Lorimore et al., 2003;Barcellos-Hoff and Mao, 2016;Hada et al., 2014;Nagasawa and Little, 1992;Belyakov et al., 2005;Chang et al., 2016).”

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Authors
Illa-Bochaca, I., Ouyang, H., Tang, J., Sebastiano, C., Mao, J.-H., Costes, S. V., Demaria, S., & Barcellos-Hoff, M. H.
Affiliations
  • New York University (US)
  • Lawrence Berkeley National Laboratory (US)
  • 1Department of Radiation Oncology, New York University School of Medicine, New York, New York.
Venue
Cancer Research
Published
2014-11-30
Volume
74
Issue
23
Pages
7137-7148
ISSN
  • 0008-5472 (ISSN-L)
  • 1538-7445
OpenAlex
W2116184323
Cited by
29
References
1
Citations by year
2026: 2 · 2025: 2 · 2024: 3 · 2022: 5 · 2021: 6 · 2020: 3 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 3
FWCI
1.30
Type
journal article
Language
en
Open access
closed
Locations
  • Cancer Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Radiation Therapy and Dosimetry
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
Keywords
high-LET radiation, radiation-induced cancer, tumor microenvironment, syngeneic tumor transplantation, cytokeratin 18, keratin 14, estrogen receptor status, metastasis, ERBB2, KRAS, E-cadherin loss, mammary stem cells, Notch signaling, gene expression profiling, radiation chimeras
MeSH terms
Animals, Female, Keratins, Mammary Neoplasms, Experimental, Mice, Inbred BALB C, Radiation, Ionizing, Receptors, Estrogen, Stem Cells, Biomarkers, Tumor, Cadherins, Tumor Suppressor Protein p53, Proto-Oncogene Proteins p21(ras), Receptor, ErbB-2, Erb-b2 Receptor Tyrosine Kinases, Gene Expression Profiling, Mice, Receptors, Notch, Tumor Microenvironment

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