Treatment of unresectable locally advanced non-small cell lung cancer includes radiotherapy which is limited by its toxicity to normal lung, particularly when treating larger-volume disease. We shall investigate a complementary biological approach to lower radiation toxicity in the normal lung included in the treatment plan, and yet increase radiation effect in the tumor target, using soy isoflavones. Mixtures of natural soy isoflavones containing genistein, daidzein and glycitein can sensitize cancer cells to ionizing radiation by inhibiting pathways of cell survival which are constitutively activated in cancer cells and not in normal cells, and are upregulated further by radiation. Soy isoflavones can also act as anti-oxidants in normal tissues thus protecting them from radiation-induced toxicity. We therefore propose that soy isoflavones could give a similar protection to irradiated normal lung, and at the same time, enhance cell killing in the tumor volume during radiotherapy, thus further improving the therapeutic effect of standard-of-care radiotherapy. The proposed studies are supported by our preliminary data demonstrating enhanced antitumor effect of radiation in human A549 xenograft lung tumor nodules in mice, and simultaneous radioprotection of the normal lung tissue by soy isoflavones.
Our specific aims are first to define the combinations of radiation dose, soy concentration and duration of soy exposure, which result in decreased survival of carcinoma cells and increased survival of normal cells using in vitro models. Then, to fully evaluate this combined modality approach in vivo, in human lung tumors growing in the lungs of nude mice, hypothesizing enhancement of effect, and to monitor changes in normal lung tissue, expecting protection against radiation damage by soy isoflavones. To achieve these aims in vitro, we shall measure cell survival by clonogenic assay, DNA damage by the 3-H2AX immunofluorescence assay and modulation of molecular pathways involved in the interaction between radiation and soy isoflavones, including APE1/Ref-1, NF-:B, HIF-11. To achieve our aims in vivo, we shall determine anti-tumor response by enumeration of lung nodules, morphometric measurements of lung sections, and by immunohistochemistry with Ki-67 proliferation marker and TUNEL assay for apoptosis as well as the use of non-invasive luminescence imaging. The effect of combining radiation with soy isoflavones in normal lung tissue, will be assessed by monitoring mouse survival and weight, DNA damage, inflammation and inflammatory cytokines, fibrosis and oxidative damage. The results of this investigation will have high impact on the management of patients diagnosed with lung cancer.

Public Health Relevance

Lung cancer can be treated more effectively using modern radiotherapy techniques which take advantage of new technologies to guide the radiation dose more precisely to the tumor target. Nevertheless, some normal lung still gets irradiated which can cause unwanted toxicity. We will investigate the capability for natural non- toxic components of soy beans to protect normal lung against radiation injury, while at the same time enhancing the effect of the radiotherapy against the malignant tumor.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21CA155518-02
Application #
8334608
Study Section
Chemo/Dietary Prevention Study Section (CDP)
Program Officer
Xi, Dan
Project Start
2011-09-19
Project End
2014-08-31
Budget Start
2012-09-01
Budget End
2014-08-31
Support Year
2
Fiscal Year
2012
Total Cost
$157,700
Indirect Cost
$53,950
Name
Wayne State University
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
001962224
City
Detroit
State
MI
Country
United States
Zip Code
48202
Abernathy, Lisa M; Fountain, Matthew D; Joiner, Michael C et al. (2017) Innate Immune Pathways Associated with Lung Radioprotection by Soy Isoflavones. Front Oncol 7:7
Fountain, Matthew D; Abernathy, Lisa M; Lonardo, Fulvio et al. (2015) Radiation-Induced Esophagitis is Mitigated by Soy Isoflavones. Front Oncol 5:238
Abernathy, Lisa M; Fountain, Matthew D; Rothstein, Shoshana E et al. (2015) Soy Isoflavones Promote Radioprotection of Normal Lung Tissue by Inhibition of Radiation-Induced Activation of Macrophages and Neutrophils. J Thorac Oncol 10:1703-12
Hillman, Gilda G; Singh-Gupta, Vinita; Lonardo, Fulvio et al. (2013) Radioprotection of lung tissue by soy isoflavones. J Thorac Oncol 8:1356-64
Hillman, Gilda G; Singh-Gupta, Vinita; Hoogstra, David J et al. (2013) Differential effect of soy isoflavones in enhancing high intensity radiotherapy and protecting lung tissue in a pre-clinical model of lung carcinoma. Radiother Oncol 109:117-25
Hillman, Gilda G; Singh-Gupta, Vinita; Runyan, Lindsay et al. (2011) Soy isoflavones radiosensitize lung cancer while mitigating normal tissue injury. Radiother Oncol 101:329-36