HS-729

Zellname

Beschreibung

Bestell-Nr.

Einheit

Preis, Euro

HS-729

Humane Rhabdomyosarkom Zell-Linie

300443

cryovial

265,00

HS-729

Humane Rhabdomyosarkom Zell-Linie

330443

vital

335,00



Designation:HS-729
ATCC Number:HTB-153
Depositor:Owens
Organism:Homo sapiens (human)
Ethnicity:caucasian
Age/Stage:74 years
Gender:male
Tissue:rhabdomyosarcoma
Morphology:fibroblast
Growth Properties:monolayer
Culture Medium:Dulbecco's modified Eagle's medium with 4.5 g/L glucose, 90%; fetal bovine serum, 10%
Subculturing:Remove medium, rinse with fresh 0.025% trypsin, 0.02% EDTA solution, remove trypsin and let the culture sit at room temperature (or at 37°C) until the cells detach (about 10 minutes). Add fresh medium, aspirate and dispense into new flasks.
Split Ratio:A ratio of 1:2 to 1:3 is recommended
Fluid Renewal:2 to 3 times weekly
Freeze Medium:CM-1, Cell Lines Service
Sterility:Tests for mycoplasma, bacteria and fungi were negative
Biosafety Level:1
DNA Profile (STR):Amelogenin: X,Y
CSF1PO: 10
D13S317: 11
D16S539: 11
D5S818: 11,12
D7S820: 8,9
TH01: 6,9.3
TPOX: 11
vWA: 16,17
D3S1358: 17
D21S11: 28,31.2
D18S51: 12
Penta E: 7,12
Penta D: 9,14
D8S1179: 10,14
FGA: 19,20
CLS – Cell Lines Service 2010.
Isoenzymes:G6PD, B


References:

The effect of 1, 25-dihydroxyvitamin D3 on the growth of soft-tissue sarcoma cells as mediated by the vitamin D receptor.
Shabahang-M; Buffan-AE; Nolla-JM; Schumaker-LM; Brenner-RV; Buras-RR; Nauta-RJ; Evans-SR
Ann-Surg-Oncol. 1996 Mar; 3(2): 144-9
BACKGROUND: Soft-tissue sarcomas, malignant neoplasms originating from mesenchymal tissue, are rare but highly aggressive tumors. Present modes of therapy are associated with high rates of recurrence. 1, 25-Dihydroxyvitamin D3, the active metabolite of vitamin D, serves as a potent antiproliferative agent in human cancer cells. METHODS: In this study, six soft-tissue sarcoma cell lines were analyzed for vitamin D receptor (VDR) expression, which was then correlated with the degree of growth inhibition in response to 1, 25-dihydroxyvitamin D3. These cell lines included rhabdomyosarcoma (HS729, A204), fibrosarcoma (HS913t), synovial sarcoma (SW982), liposarcoma (SW872), and leiomyosarcoma (SKLMS-1). The level of VDR messenger RNA (mRNA) expression was determined using a ribonuclease protection assay, and functional receptor content was determined by using a ligand-binding assay. Growth studies, including [3H]thymidine uptake and growth curves, were performed on two of the six cell lines that expressed the highest and lowest receptor levels. RESULTS: Ribonuclease protection and ligand-binding assays demonstrated variable levels of VDR, with HS729 showing high expression and A204 showing no expression. In HS729, [3H]thymidine uptake was significantly decreased at 10(-7) M (33%) and 10(-6) M (40%) 1, 25-dihydroxyvitamin D3. Growth curve studies showed significant growth inhibition of 55% at 10(-6) M. A204 cells showed no growth inhibition upon treatment with 1, 25-dihydroxyvitamin D3. CONCLUSION: This study demonstrates the existence of VDR in soft-tissue sarcoma cells and suggests a correlation between the level of VDR in cells and the degree of growth inhibition caused by 1, 25-dihydroxyvitamin D3 which may potentially serve as an alternative form of therapy for soft-tissue sarcomas.

 

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