STEM-14. GROWTH FACTOR RECEPTOR CO-INHERITANCE DURING ASYMMETRIC CELL DIVISION DRIVES THE CANCER STEM CELL PHENOTYPE. (5th November 2018)

• Record Type: Journal Article
• Authors: Hitomi, Masahiro; Chumakova, Anastasia; Jarvis, Stephanie; Anand, Neha; Silver, Daniel; Knudsen, Arnon; Corrigan, Bridget; Yoo, Peter; Agrawal, Upashruti; Pfaff, Kayla; Yogeswaran, Vid; Kaminen, Malini; Sato, Masahiko; Sato, Sachiko; W. Kristensen, Bjarne; Lathia, Justin
• Is Part Of: Neuro-oncology. Volume 20(2018)Supplement 6
• Page Start: vi246
• Page End: vi246
• Publication Date: 2018-11-05
• Subjects: Brain Neoplasms -- Periodicals; Brain -- Tumors -- Periodicals; Brain -- Cancer -- Periodicals; Nervous system -- Cancer -- Periodicals; 616.99481
• DOI: 10.1093/neuonc/noy148.1021
• Languages: English
• ISSNs: 1522-8517

Abstract

Abstract: An asymmetric cell division (ACD) produces a stem cell and a differentiating progeny. Thus ACD ensures the generation of organs with heterogeneous cell populations without depleting pools of stem cells with regenerative capacity. Cancer stem cells (CSCs), which are similar to normal stem cells, can self-renew and regenerate tumors with cellular heterogeneity. CSCs are resistant to therapy and play a critical role in tumor recurrence. ACD has been detected in CSCs from many types of tumors, but its role in CSC fate decision has yet to be fully elucidated. A remaining technical limitation is that ACD is often defined retrospectively based on the observation of an asymmetric fate choice by CSC progeny. We previously demonstrated asymmetric inheritance of a surrogate CSC marker, CD133, during mitosis. To prospectively analyze the biological role of this inheritance asymmetry, we have developed a GFP reporter system capable of monitoring the degree of asymmetry of the CSC marker during mitosis. This reporter also revealed the asymmetric co-inheritance of growth factor receptors, the activation of which overrode the effect of a differentiation-inducing condition that suppresses self-renewal capacity and therapeutic resistance of CSCs. Preliminary time lapse-based lineage tracing detected that daughter cells that inherited higher levels of growth factor receptors based on GFP-reporter signal intensity express higher levels of a core stem cell transcription factor compared to their sister cells that inherited lower levels of growth factor receptors. These data suggest that asymmetrically co-inherited growth factor receptors promote the stem cell state in one of the progeny of a CSC undergoing ACD, ensuring the persistence of a therapeutically resistant population.