A novel and cost-effective
| Autor: | Akash, Gupta, Geetanjali, Gupta, Rajeshwari R, Mehta, David Z, Ivancic, Rashidra R, Walker, Jankiben R, Patel, Karen M, Gallegos, A Michael, Davidson, Seema A, Khan, Rajendra G, Mehta, Syreeta L, Tilghman |
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| Rok vydání: | 2020 |
| Předmět: |
Cost-Benefit Analysis
Orthotopic model Mammary gland Mammary Neoplasms Experimental Breast Neoplasms Xenograft Model Antitumor Assays Antioxidant Response Elements Organ culture Disease Models Animal Mice Organ Culture Techniques Cell Line Tumor Biomarkers Tumor Animals Humans Female Breast cancer model Disease Susceptibility skin and connective tissue diseases Promoter Regions Genetic Cells Cultured Research Article |
| Zdroj: | Biology Open article-version (VoR) Version of Record |
| ISSN: | 2046-6390 |
| Popis: | Mouse mammary organ culture (MMOC) is used to evaluate the efficacy of chemopreventive agents against the development of carcinogen-induced preneoplastic lesions and is highly correlative to in vivo carcinogenesis models. Here, we developed a new ex vivo MMOC model, by introducing human breast cancer cells into the mouse mammary gland. This novel model, termed human breast cancer in MMOC (BCa-MMOC), mimics in vivo orthotopic breast cancer mouse models. To develop this model, estradiol- and progesterone-sensitized female mice were injected with letrozole-sensitive and -resistant T47D breast cancer cells in the mammary glands and then euthanized. The glands were cultured in vitro with hormone-supplemented media. On day 25, the glands were fixed and processed by histopathology and immunohistochemistry to evaluate for the presence of T47D cells, growth pattern, cancer markers and estradiol responsiveness. Histopathological analyses demonstrated an identical pattern of growth between the breast cancer cells injected ex vivo and in vivo. Interestingly, clusters of cancer cells in the mammary gland stroma appeared similar to those observed in human breast tumors. The injected T47D cells survived and proliferated for 15 days maintaining expression of estrogen receptor alpha (ER), progesterone receptor (PR), epidermal growth factor receptor (EGFR), and aromatase. The aromatase-overexpressing T47D grown in the BCa-MMOC sufficiently metabolized estrogen, resulting in enhanced cell proliferation, induction of estrogen target genes (i.e. ER and PR-B), and showed typical changes to estrogenic milieu. In summary, here we show a novel, inexpensive ex vivo model, to potentially study the effects of therapeutic agents on cancer cells grown in an orthotopic micromilieu. This article has an associated First Person interview with the first author of the paper. Summary: Here, we describe and validate a novel, cost-effective ex vivo orthotopic model to evaluate chemotherapy agents for breast cancer. |
| Databáze: | OpenAIRE |
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