Description:
NEUROBLASTOMA; NB NEUROBLASTOMA SUPPRESSOR, INCLUDED; NBS, INCLUDED
TRANSLOCATED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases Chromosome Abnormalities |
Class |
Disorders of the Nervous System |
Cell Type
|
Fibroblast
|
Tissue Type
|
Tumor
|
Transformant
|
Untransformed
|
Race
|
White
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
|
ISCN
|
47,X,-Y,+13,+19p+,9q-,11q-,19p+
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis |
|
Remarks |
Stage IV; patient expired at age 16 months; at 15 months, developed 'raccoon eyes' and bone metastases; monolayer culture, which may pile up, grows slowly; originated from tumor tissue passaged in a nude mouse; 47,X,-Y, +13,+19p+,9q-,11q-,19p+; pass 1 at CCR |
Colella R, Lu G, Glazewski L, Korant B, Matlapudi A, England MR, Craft C, Frantz CN, Mason RW, Induction of cell death in neuroblastoma by inhibition of cathepsins B and L Cancer letters294:195-203 2009 |
PubMed ID: 20362389 |
Split Ratio |
1:5 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Ham's F12 Medium/RPMI 1640 Medium, 1:1 mixture with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
|
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