Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Enzyme
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Query: UMLS:C0027819 (
neuroblastoma
)
27,800
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Large-scale hemizygous loss of chromosome 3p is a common event in
neuroblastoma
, occurring preferentially in tumors that exhibit loss of chromosome 11q and lack MYCN amplification. Although numerous tumor suppressor genes (TSG) have been mapped to the 3p region, the gene or genes contributing to
neuroblastoma
pathogenesis have remained elusive. High-resolution oligonucleotide array CGH mapping of chromosome 3p breakpoints relative to the positions of known TSGs indicates that more than one gene may contribute to
neuroblastoma
pathogenesis. We evaluated the methylation status of
semaphorin 3B
(
SEMA3B
), one of the chromosome 3p TSGs, in
neuroblastoma
tumors with (n = 12) and without (n = 32) 3p deletions. A significantly higher percentage of methylated CpG sites in the
SEMA3B
promoter was detected in tumors exhibiting 3p loss (95%), relative to tumors without loss (52%), suggestive of a two-hit mechanism of allele inactivation. The involvement of methylation in the control of
SEMA3B
expression was confirmed by treatment of
neuroblastoma
cell lines with the demethylating agent 5-aza-2-deoxycytidine. Transcriptional regulation of this locus is complex, however; low levels of
SEMA3B
expression were also seen in tumors with unmethylated
SEMA3B
promoters (n = 4).
SEMA3B
is known to play an important role in the development of normal sympathetic neurons, and interestingly, we found higher levels of
SEMA3B
expression in differentiated tumors with favorable histopathology (n = 19) than in tumors with unfavorable histology (n = 22). Furthermore,
SEMA3B
was upregulated in the SK-N-BE
neuroblastoma
cell line following induction of differentiation with retinoic acid. The association of
SEMA3B
expression with
neuroblastoma
differentiation suggests that this TSG may play a role in
neuroblastoma
pathobiology.
...
PMID:High-resolution analysis of 3p deletion in neuroblastoma and differential methylation of the SEMA3B tumor suppressor gene. 1745 50