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Human cerebrospinal fluid affects chemoradiotherapy sensitivities in tumor cells from patients with glioblastoma

Title: Human cerebrospinal fluid affects chemoradiotherapy sensitivities in tumor cells from patients with glioblastoma
Authors: Stringer, Brett W.; De Silva, Manam Inushi; Greenberg, Zarina; Noreña Puerta, Alejandra; Adams, Robert; Milky, Bridget; Zabolocki, Michael; van den Hurk, Mark; Ebert, Lisa M.; Fairly Bishop, Christine; Conn, Simon J.; Kichenadasse, Ganessan; Michael, Michael Z.; Ormsby, Rebecca J.; Poonoose, Santosh; Bardy, Cedric
Source: Science Advances ; volume 9, issue 43 ; ISSN 2375-2548
Publisher Information: American Association for the Advancement of Science (AAAS)
Publication Year: 2023
Description: Cancers in the central nervous system resist therapies effective in other cancers, possibly due to the unique biochemistry of the human brain microenvironment composed of cerebrospinal fluid (CSF). However, the impact of CSF on cancer cells and therapeutic efficacy is unknown. Here, we examined the effect of human CSF on glioblastoma (GBM) tumors from 25 patients. We found that CSF induces tumor cell plasticity and resistance to standard GBM treatments (temozolomide and irradiation). We identified nuclear protein 1 (NUPR1), a transcription factor hampering ferroptosis, as a mediator of therapeutic resistance in CSF. NUPR1 inhibition with a repurposed antipsychotic, trifluoperazine, enhanced the killing of GBM cells resistant to chemoradiation in CSF. The same chemo-effective doses of trifluoperazine were safe for human neurons and astrocytes derived from pluripotent stem cells. These findings reveal that chemoradiation efficacy decreases in human CSF and suggest that combining trifluoperazine with standard care may improve the survival of patients with GBM.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1126/sciadv.adf1332
Availability: https://doi.org/10.1126/sciadv.adf1332; https://www.science.org/doi/pdf/10.1126/sciadv.adf1332
Accession Number: edsbas.669C950F
Database: BASE