Establishing and Characterizing Chemotherapy-Induced Immunological Dormant Tumor Cell Lines.
Qiang LanSanam PeyvandiCurzio RueggPublished in: Methods in molecular biology (Clifton, N.J.) (2024)
Chemotherapy, together with radiotherapy, targeted therapies, and immunotherapy, is the main option to treat cancer patients in neoadjuvant/adjuvant setting to reduce the risk of disease progression and metastasis formation from disseminated tumor cells. Cancer cells that survived chemotherapy treatment may emerge with novel characteristics, one of which is the ability to stimulate the native and adaptive immune systems. Models allowing the characterization of chemotherapy-induced tumor cell plasticity and induction of immune response or adaptation are needed to identify novel mechanisms and devise novel therapeutic strategies to prevent relapses. Here we describe a protocol for selecting chemotherapy-resistant cancer cells and testing the in vivo effects on the local and systemic immune responses. While originally developed to characterize the effects of methotrexate and doxorubicin on murine 4T1 breast cancer cells and the relative immune response, the method can be broadened to other chemotherapies and syngeneic cancer models.
Keyphrases
- chemotherapy induced
- immune response
- locally advanced
- early stage
- breast cancer cells
- dendritic cells
- toll like receptor
- rectal cancer
- papillary thyroid
- randomized controlled trial
- single cell
- squamous cell carcinoma
- radiation therapy
- lymph node
- drug delivery
- cell therapy
- high dose
- radiation induced
- squamous cell
- stem cells
- mesenchymal stem cells
- young adults
- combination therapy
- lymph node metastasis