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Modeling Brain Metastasis Via Tail-Vein Injection of Inflammatory Breast Cancer Cells.
Hu, Xiaoding; Villodre, Emilly S; Woodward, Wendy A; Debeb, Bisrat G.
Afiliación
  • Hu X; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center; Morgan Welch Inflammatory Breast Cancer Clinic and Research Program, The University of Texas MD Anderson Cancer Center.
  • Villodre ES; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center; Morgan Welch Inflammatory Breast Cancer Clinic and Research Program, The University of Texas MD Anderson Cancer Center.
  • Woodward WA; Morgan Welch Inflammatory Breast Cancer Clinic and Research Program, The University of Texas MD Anderson Cancer Center; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center.
  • Debeb BG; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center; Morgan Welch Inflammatory Breast Cancer Clinic and Research Program, The University of Texas MD Anderson Cancer Center; bgdebeb@mdanderson.org.
J Vis Exp ; (168)2021 02 04.
Article en En | MEDLINE | ID: mdl-33616115
Metastatic spread to the brain is a common and devastating manifestation of many types of cancer. In the United States alone, about 200,000 patients are diagnosed with brain metastases each year. Significant progress has been made in improving survival outcomes for patients with primary breast cancer and systemic malignancies; however, the dismal prognosis for patients with clinical brain metastases highlights the urgent need to develop novel therapeutic agents and strategies against this deadly disease. The lack of suitable experimental models has been one of the major hurdles impeding advancement of our understanding of brain metastasis biology and treatment. Herein, we describe a xenograft mouse model of brain metastasis generated via tail-vein injection of an endogenously HER2-amplified cell line derived from inflammatory breast cancer (IBC), a rare and aggressive form of breast cancer. Cells were labeled with firefly luciferase and green fluorescence protein to monitor brain metastasis, and quantified metastatic burden by bioluminescence imaging, fluorescent stereomicroscopy, and histologic evaluation. Mice robustly and consistently develop brain metastases, allowing investigation of key mediators in the metastatic process and the development of preclinical testing of new treatment strategies.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Luciferasas de Luciérnaga / Neoplasias Inflamatorias de la Mama / Rastreo Celular / Inyecciones Intravenosas Idioma: En Revista: J Vis Exp Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Luciferasas de Luciérnaga / Neoplasias Inflamatorias de la Mama / Rastreo Celular / Inyecciones Intravenosas Idioma: En Revista: J Vis Exp Año: 2021 Tipo del documento: Article