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Association of Aggresomes with Survival Outcomes in Pediatric Medulloblastoma.


ABSTRACT: Aggresomes are inclusion bodies for misfolded/aggregated proteins. Despite the role of misfolded/aggregated proteins in neurological disorders, their role in cancer pathogenesis is poorly defined. In the current study we aimed to investigate whether aggresomes-positivity could be used to improve the disease subclassification and prognosis prediction of pediatric medulloblastoma. Ninety three pediatric medulloblastoma tumor samples were retrospectively stratified into three molecular subgroups; WNT, SHH and non-WNT/non-SHH, using immunohistochemistry and Multiplex Ligation Probe Amplification. Formation of aggresomes were detected using immunohistochemistry. Overall survival (OS) and event-free survival (EFS) were determined according to risk stratification criteria. Multivariate Cox regression analyses were carried out to exclude confounders. Aggresomes formation was detected in 63.4% (n?=?59/93) of samples. Aggresomes were non-randomly distributed among different molecular subgroups (P?=?0.00002). Multivariate Cox model identified aggresomes' percentage at ?20% to be significantly correlated with patient outcome in both OS (HR?=?3.419; 95% CI, 1.30-8.93; P?=?0.01) and EFS (HR?=?3; 95% CI, 1.19-7.53; P?=?0.02). The presence of aggresomes in ?20% of the tumor identified poor responders in standard risk patients; OS (P?=?0.02) and EFS (P?=?0.06), and significantly correlated with poor outcome in non-WNT/non-SHH molecular subgroup; OS (P?=?0.0002) and EFS (P?=?0.0004).

SUBMITTER: Yehia M 

PROVIDER: S-EPMC6717208 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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Aggresomes are inclusion bodies for misfolded/aggregated proteins. Despite the role of misfolded/aggregated proteins in neurological disorders, their role in cancer pathogenesis is poorly defined. In the current study we aimed to investigate whether aggresomes-positivity could be used to improve the disease subclassification and prognosis prediction of pediatric medulloblastoma. Ninety three pediatric medulloblastoma tumor samples were retrospectively stratified into three molecular subgroups; W  ...[more]

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