Publications by authors named "Blake Morrison"

Article Synopsis
  • Lung cancer cells, particularly NSCLC, increase their ability to survive oxidative stress by upregulating the xCT transporter for cystine, which helps maintain high intracellular cysteine levels necessary for making glutathione.* -
  • The NRF2 transcription factor regulates the xCT transporter and is kept in check by KEAP1; mutations in KEAP1 or NRF2 can enhance cystine uptake and support cancer cell survival, while limited cystine can lead to ferroptosis, a form of cell death.* -
  • Targeted therapies in certain NSCLC types can trigger pyroptosis and apoptosis, leading to the breakdown of the cell membrane after caspase-3 activation, contributing to death of the cancer cells.*
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Bortezomib synergizes with melphalan in preclinical and early clinical studies. Updated data from our phase 1/2 study assessing the safety and efficacy of bortezomib plus melphalan in relapsed/refractory multiple myeloma (MM) are presented. Bortezomib (0.

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Purpose: This multicenter, open-label, phase I/II dose escalation study assessed the safety/tolerability and initial efficacy of arsenic trioxide/bortezomib/ascorbic acid (ABC) combination therapy in patients with relapsed/refractory multiple myeloma.

Experimental Design: Enrolled in six cohorts, patients were given arsenic trioxide (0.125 or 0.

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Purpose: Bortezomib has shown synergy with melphalan in preclinical models. We assessed the safety, tolerability, and response rate in a dose-escalation study of this combination for relapsed or refractory multiple myeloma patients.

Methods: Bortezomib was administered from 0.

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