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Retinoblastoma family proteins induce differentiation and regulate B-myb expression in neuroblastoma cells
Medical and pediatric oncology, 2001-01, Vol.36 (1), p.104-107
Raschellà, Giuseppe
Tanno, Barbara
Bonetto, Francesco
Negroni, Anna
Amendola, Roberto
Paggi, Marco G.
2001
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Raschellà, Giuseppe
Tanno, Barbara
Bonetto, Francesco
Negroni, Anna
Amendola, Roberto
Paggi, Marco G.
Titel
Retinoblastoma family proteins induce differentiation and regulate B-myb expression in neuroblastoma cells
Ist Teil von
Medical and pediatric oncology, 2001-01, Vol.36 (1), p.104-107
Ort / Verlag
New York: John Wiley & Sons, Inc
Erscheinungsjahr
2001
Quelle
Wiley-Blackwell Journals
Beschreibungen/Notizen
Background The expression of several genes is modulated during neuroblastoma differentiation. The retinoblastoma family proteins, pRb, p107 and pRb2/p130, act in the repression of proliferation genes, interacting mainly with the E2F transcription factors. Procedure and Results In this study, we found that, in neuroblastoma cell lines, pRb and p107 proteins decreased, undergoing progressive dephosphorylation, whereas pRb2/p130 increased at late stages of differentiation. B‐myb expression was down‐regulated in association with the up‐regulation of pRb2/p130, the major partner of E2F on the E2F site of the B‐myb promoter in differentiated cells. Transfection of each of the retinoblastoma family genes in neuroblastoma cells was able to induce neural differentiation, to inhibit 3H‐thymidine incorporation, and to down‐regulate B‐myb promoter activity. Conclusions In conclusion, our data suggest a major contribution of retinoblastoma proteins, and especially of pRb2/p130, in B‐myb promoter regulation and demonstrate the induction of neural differentiation by p107 and pRb2/p130, suggesting a role of these proteins in triggering differentiation‐specific genes. Med. Pediatr. Oncol. 36:104–107, 2001. © 2001 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0098-1532
eISSN: 1096-911X
DOI: 10.1002/1096-911X(20010101)36:1<104::AID-MPO1024>3.0.CO;2-9
Titel-ID: cdi_proquest_miscellaneous_71026223
Format
–
Schlagworte
Animals
,
B-myb
,
Cell Cycle Proteins
,
Cell Differentiation - drug effects
,
differentiation
,
Dimethyl Sulfoxide - pharmacology
,
DNA-Binding Proteins - biosynthesis
,
E2F
,
E2F Transcription Factors
,
Gene Expression Regulation, Neoplastic
,
Genes, myb
,
Genes, Reporter
,
Genes, Retinoblastoma
,
Humans
,
Luciferases - biosynthesis
,
Mice
,
Neoplasm Proteins - genetics
,
Neoplasm Proteins - physiology
,
neuroblastoma
,
Neuroblastoma - genetics
,
Neuroblastoma - pathology
,
Nuclear Proteins - genetics
,
Nuclear Proteins - physiology
,
p107
,
Phosphoproteins - genetics
,
Phosphoproteins - physiology
,
pRb
,
pRb2/p130
,
Promoter Regions, Genetic
,
Proteins
,
Recombinant Fusion Proteins - biosynthesis
,
retinoblastoma family
,
Retinoblastoma Protein - physiology
,
Retinoblastoma-Like Protein p107
,
Retinoblastoma-Like Protein p130
,
Trans-Activators - biosynthesis
,
Transcription Factors - physiology
,
Transfection
,
Tretinoin - pharmacology
,
Tumor Cells, Cultured - drug effects
,
Tumor Cells, Cultured - metabolism
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