Results 21 to 30 of about 137,730 (260)

Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma

open access: yesBMC Pediatrics, 2021
Background MYCN amplification and age are two critical prognostic factors of pediatric neuroblastoma. Previously, we had revealed the prognosis of MYCN target genes.
Haiwei Wang   +4 more
doaj   +1 more source

AKT inhibitor Hu7691 induces differentiation of neuroblastoma cells

open access: yesActa Pharmaceutica Sinica B, 2023
While neuroblastoma accounts for 15% of childhood tumor-related deaths, treatments against neuroblastoma remain scarce and mainly consist of cytotoxic chemotherapeutic drugs.
Shaowei Bing   +12 more
doaj   +1 more source

CRISPR/Cas9-based genome-wide screening of the deubiquitinase subfamily identifies USP3 as a protein stabilizer of REST blocking neuronal differentiation and promotes neuroblastoma tumorigenesis

open access: yesJournal of Experimental & Clinical Cancer Research, 2023
Background The repressor element-1 silencing transcription factor (REST), a master transcriptional repressor, is essential for maintenance, self-renewal, and differentiation in neuroblastoma.
Janardhan Keshav Karapurkar   +9 more
doaj   +1 more source

Autophagy inhibition improves the cytotoxic effects of receptor tyrosine kinase inhibitors

open access: yesCancer Cell International, 2018
Background A growing field of evidence suggests the involvement of oncogenic receptor tyrosine kinases (RTKs) in cell transformation. Deregulated activity of RTKs in tumors can determine disease progression and therapeutic responses in several types of ...
Sanja Aveic   +7 more
doaj   +1 more source

Prognostic analysis of E2F transcription factors E2F1 and E2F3 in four independent pediatric neuroblastoma cohorts

open access: yesBMC Pediatrics, 2022
Background Previously, we had analyzed the prognosis of E2F transcription factors across adult tumor types. However, the expressions and prognosis of E2F transcription factors in pediatric neuroblastoma have not yet been fully studied.
Haiwei Wang   +3 more
doaj   +1 more source

NEUROBLASTOMA [PDF]

open access: yesSeminars in Pediatric Surgery, 2010
Neuroblastoma is a heterogeneous disease; tumors can spontaneously regress or mature, or display an aggressive, therapy-resistant phenotype. Increasing evidence indicates that the biological and molecular features of neuroblastoma significantly influence and are highly predictive of clinical behavior.
openaire   +2 more sources

Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours

open access: yesBMC Cancer, 2019
Background Neuroblastoma (NB) is a paediatric tumour of the sympathetic nervous system. Half of all cases are defined high-risk with an overall survival less than 40% at 5 years from diagnosis.
P. Fusco   +13 more
doaj   +1 more source

RTEL1 gene polymorphisms and neuroblastoma risk in Chinese children

open access: yesBMC Cancer, 2023
Background Neuroblastoma, a neuroendocrine tumor originating from the sympathetic ganglia, is one of the most common malignancies in childhood. RTEL1 is critical in many fundamental cellular processes, such as DNA replication, DNA damage repair, genomic ...
Ting Zhang   +5 more
doaj   +1 more source

Neuroblastoma [PDF]

open access: yesJapanese Journal of Clinical Oncology, 2018
Neuroblastoma is one of the most common solid tumors in children and has a diverse clinical behavior that largely depends on the tumor biology. Neuroblastoma exhibits unique features, such as early age of onset, high frequency of metastatic disease at diagnosis in patients over 1 year of age and the tendency for spontaneous regression of tumors in ...
Akira, Nakagawara   +5 more
openaire   +2 more sources

EZH2 inhibition decreases neuroblastoma proliferation and in vivo tumor growth.

open access: yesPLoS ONE, 2021
Investigation of the mechanisms responsible for aggressive neuroblastoma and its poor prognosis is critical to identify novel therapeutic targets and improve survival.
Laura V Bownes   +11 more
doaj   +1 more source

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