Javascript must be enabled to continue!
Abstract 5403: Targeting death-receptors in therapy resistant progressive neuroblastoma: A preliminary insight
View through CrossRef
Abstract
Neuroblastoma is the most common cancer in infants and accounts for 9.1% of childhood cancer-related deaths. Despite the current standard of care (SOC), drug-resistant neuroblastoma significantly compromises patient survival. Hence it is critical to identify new and less toxic therapeutic approaches for better patient outcomes. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), which mediates its effect through the activation of the death receptor (DR) 4 and 5 are found on many cell types and are the main pathway for apoptosis. These can death receptors can kill most tumor cell types expressing TRAIL-receptor 1. Mining RNA-Seq data across multiple cohorts of neuroblastoma patients indicated that high levels of DR4 and DR5 significantly associated with poor clinical outcomes (OS, EFS, RFS). Further, examining the surface expression of DR4 and DR5 by immunohistochemistry using anti-human rabbit monoclonal antibodies on custom-archived TMAs for 100 NB patients revealed profound correlation with poor OS and RFS. Immunoblot analysis for DR4 and DR5 level in a panel of stage 4 patient-derived cell-lines during diagnosis and from progressive disease after therapy displayed high-levels of death receptor expression in progressive disease. Preliminary co-culture investigations with genetically engineered mesenchymal stem cells (MSCs) expressing tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) mimicking targeted delivery showed heightened differentiation and death (limited dilution tumorosphere assay) of therapy resistant cells. Further these studies exhibited inhibition of tumor cell migration and invasion. The results demonstrate the benefit of targeted TRAIL delivery in in the treatment of therapy resistant neuroblastoma and further imply that the genetically engineered MSCs could serve as a clinically valuable tool for improved therapeutic strategy in this setting.
Citation Format: Dinesh Babu Somasundaram, Andrew Maher, Sheeja Aravindan, Terence S. Herman, Natarajan Aravindan. Targeting death-receptors in therapy resistant progressive neuroblastoma: A preliminary insight [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 5403.
American Association for Cancer Research (AACR)
Title: Abstract 5403: Targeting death-receptors in therapy resistant progressive neuroblastoma: A preliminary insight
Description:
Abstract
Neuroblastoma is the most common cancer in infants and accounts for 9.
1% of childhood cancer-related deaths.
Despite the current standard of care (SOC), drug-resistant neuroblastoma significantly compromises patient survival.
Hence it is critical to identify new and less toxic therapeutic approaches for better patient outcomes.
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), which mediates its effect through the activation of the death receptor (DR) 4 and 5 are found on many cell types and are the main pathway for apoptosis.
These can death receptors can kill most tumor cell types expressing TRAIL-receptor 1.
Mining RNA-Seq data across multiple cohorts of neuroblastoma patients indicated that high levels of DR4 and DR5 significantly associated with poor clinical outcomes (OS, EFS, RFS).
Further, examining the surface expression of DR4 and DR5 by immunohistochemistry using anti-human rabbit monoclonal antibodies on custom-archived TMAs for 100 NB patients revealed profound correlation with poor OS and RFS.
Immunoblot analysis for DR4 and DR5 level in a panel of stage 4 patient-derived cell-lines during diagnosis and from progressive disease after therapy displayed high-levels of death receptor expression in progressive disease.
Preliminary co-culture investigations with genetically engineered mesenchymal stem cells (MSCs) expressing tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) mimicking targeted delivery showed heightened differentiation and death (limited dilution tumorosphere assay) of therapy resistant cells.
Further these studies exhibited inhibition of tumor cell migration and invasion.
The results demonstrate the benefit of targeted TRAIL delivery in in the treatment of therapy resistant neuroblastoma and further imply that the genetically engineered MSCs could serve as a clinically valuable tool for improved therapeutic strategy in this setting.
Citation Format: Dinesh Babu Somasundaram, Andrew Maher, Sheeja Aravindan, Terence S.
Herman, Natarajan Aravindan.
Targeting death-receptors in therapy resistant progressive neuroblastoma: A preliminary insight [abstract].
In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24.
Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 5403.
Related Results
Are Cervical Ribs Indicators of Childhood Cancer? A Narrative Review
Are Cervical Ribs Indicators of Childhood Cancer? A Narrative Review
Abstract
A cervical rib (CR), also known as a supernumerary or extra rib, is an additional rib that forms above the first rib, resulting from the overgrowth of the transverse proce...
Abstract LB221: Novel molecular targeted tumor targeted oncolytic peptide for the treatment of therapy resistant progressive neuroblastoma
Abstract LB221: Novel molecular targeted tumor targeted oncolytic peptide for the treatment of therapy resistant progressive neuroblastoma
Abstract
Cancer treatments, particularly for solid tumors like neuroblastoma, often entail severe side effects, resistance, and the potential for secondary malignanc...
Abstract 4758: Inhibition of checkpoint kinase 1 (Chk1) as a potential therapeutic for pediatric neuroblastoma
Abstract 4758: Inhibition of checkpoint kinase 1 (Chk1) as a potential therapeutic for pediatric neuroblastoma
Abstract
Neuroblastoma is a cancer derived from cells of the sympathetic nervous system that manifests with significant clinical heterogeneity. Although children dia...
Data from A NOTCH3 Transcriptional Module Induces Cell Motility in Neuroblastoma
Data from A NOTCH3 Transcriptional Module Induces Cell Motility in Neuroblastoma
<div>Abstract<p><b>Purpose:</b> Neuroblastoma is a childhood tumor of the peripheral sympathetic nervous system with an often lethal outcome due to metastat...
Data from A NOTCH3 Transcriptional Module Induces Cell Motility in Neuroblastoma
Data from A NOTCH3 Transcriptional Module Induces Cell Motility in Neuroblastoma
<div>Abstract<p><b>Purpose:</b> Neuroblastoma is a childhood tumor of the peripheral sympathetic nervous system with an often lethal outcome due to metastat...
Pet Euthanasia and Human Euthanasia
Pet Euthanasia and Human Euthanasia
Photo ID 213552852 © Yuryz | Dreamstime.com
Abstract
A criticism of assisted death is that it’s contrary to the Hippocratic Oath. This opposition to assisted death assumes that dea...
The Dopamine Receptors
The Dopamine Receptors
Abstract
Dopamine receptors have a prominent place in our understanding of brain function. Drugs blocking dopamine receptors are used as antipsy...
Abstract LB015: Differential expression of deubiquitinating enzymes and its related DNA damage response genes in neuroblastoma heterogeneity
Abstract LB015: Differential expression of deubiquitinating enzymes and its related DNA damage response genes in neuroblastoma heterogeneity
Abstract
SK-N-AS and SK-N-DZ are two cell lines of pediatric solid tumors neuroblastomas well characterized to evaluate heterogeneity between different neuroblastoma...

