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3D tissue engineered plasma cultures support leukemic proliferation and induces drug resistance.
Alhallak, Kinan; de la Puente, Pilar; Jeske, Amanda; Sun, Jennifer; Muz, Barbara; Rettig, Michael P; Sahin, Ilyas; Weisberg, Ellen L; Griffin, James D; Reagan, John L; DiPersio, John F; Azab, Abdel Kareem.
Afiliação
  • Alhallak K; Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
  • de la Puente P; Department of Biomedical Engineering, Washington University, St. Louis, MO, USA.
  • Jeske A; Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
  • Sun J; Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
  • Muz B; Department of Biomedical Engineering, Washington University, St. Louis, MO, USA.
  • Rettig MP; Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
  • Sahin I; Department of Biomedical Engineering, Washington University, St. Louis, MO, USA.
  • Weisberg EL; Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
  • Griffin JD; Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
  • Reagan JL; Division of Hematology and Oncology, The Warren Alpert Medical School of Brown University, Providence, RI, USA.
  • DiPersio JF; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Azab AK; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Leuk Lymphoma ; 62(10): 2457-2465, 2021 10.
Article em En | MEDLINE | ID: mdl-33993837
ABSTRACT
Chronic myeloid leukemia (CML), acute myeloid leukemia (AML), and chronic lymphocytic leukemia (CLL) are hematological malignancies that remain incurable despite novel treatments. In order to improve current treatments and clinical efficacy, there remains a need for more complex in vitro models that mimic the intricate human leukemic microenvironment. This study aimed to use 3D tissue engineered plasma cultures (3DTEPC) derived from CML, AML and CLL patients to promote proliferation of leukemic cells for use as a drug screening tool for treatment. 3DTEPC supported the growth of primary CML, AML and CLL cells and also induced significantly more drug resistance in CML, AML and CLL cell lines compared to 2D. The 3DTEPC created a more physiologically relevant environment for leukemia cell proliferation, provided a reliable model for growing leukemia patient samples, and serves as a relevant tool for drug screening and personalized medicine.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Leucemia Mielogênica Crônica BCR-ABL Positiva / Leucemia Mieloide Aguda Limite: Humans Idioma: En Revista: Leuk Lymphoma Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Leucemia Mielogênica Crônica BCR-ABL Positiva / Leucemia Mieloide Aguda Limite: Humans Idioma: En Revista: Leuk Lymphoma Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos