Publications by authors named "Arin N Graner"

Chordomas are rare, generally slow-growing spinal tumors that nonetheless exhibit progressive characteristics over time, leading to malignant phenotypes and high recurrence rates, despite maximal therapeutic interventions. The tumors are notoriously resistant to therapies and are often located in regions that complicate achieving gross total resections. Cell lines from these tumors are rare as well.

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Glioblastomas (GBMs) are dreadful brain tumors with abysmal survival outcomes. GBM extracellular vesicles (EVs) dramatically affect normal brain cells (largely astrocytes) constituting the tumor microenvironment (TME). We asked if EVs from different GBM patient-derived spheroid lines would differentially alter recipient brain cell phenotypes.

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Glioblastomas (GBMs) are dreadful brain tumors with abysmal survival outcomes. GBM EVs dramatically affect normal brain cells (largely astrocytes) constituting the tumor microenvironment (TME). EVs from different patient-derived GBM spheroids induced differential transcriptomic, secretomic, and proteomic effects on cultured astrocytes/brain tissue slices as GBM EV recipients.

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Article Synopsis
  • Glioblastoma (GBM) is identified as the deadliest type of brain tumor, and extracellular vesicles (EVs) from these tumors significantly influence tumor growth and invasion by communicating with other cells in the environment.
  • Researchers isolated and analyzed EVs from the blood of GBM patients, meningioma patients, and healthy individuals, finding that GBM EVs are smaller and have distinct characteristics.
  • The study showed that GBM EVs can induce cell death in neurons and neuroblastoma cells through immunological mechanisms, suggesting that these EVs play a key role in the damage caused by the tumor.
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Background: Agents targeting HSP90 and GRP94 are seldom tested in stressed contexts such as heat shock (HS) or the unfolded protein response (UPR). Tumor stress often activates HSPs and the UPR as pro-survival mechanisms. This begs the question of stress effects on chemotherapeutic efficacy, particularly with drugs targeting chaperones such as HSP90 or GRP94.

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