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CRD-BP: A c-myc mRNA stabilizing protein with an oncofetal pattern of expression

Title
CRD-BP: A c-myc mRNA stabilizing protein with an oncofetal pattern of expression
Type
Article in International Scientific Journal
Year
2003
Authors
Ioannidis, P
(Author)
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Mahaira, L
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Papadopoulou, A
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Heim, S
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Andersen, JA
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Evangelou, E
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Dafni, U
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Pandis, N
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Trangas, T
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Journal
Title: Anticancer ResearchImported from Authenticus Search for Journal Publications
Vol. 23
Pages: 2179-2183
ISSN: 0250-7005
Other information
Authenticus ID: P-000-GQY
Abstract (EN): The Coding Region Determinant-Binding Protein (CRD-BP) is an RRM and KH-domain-containing protein that recognizes specifically at least three RNAs. It binds to one of the two c-myc mRNA instability elements, to the 5'Un Translated Region (UTR) of the leader 3 IGF-II mRNA and to the oncofetal H19 RNA. CRD-BP has been assigned a role in stabilizing c-myc mRNA by preventing its endonucleolytic cleavage and in repressing the translation of the leader 3 IGF-II mRNA, the major embryonic species of this message. CRD-BP is normally expressed only in fetal tissues. However, its expression is detected in primary tumors and transformed cell lines of different origins. The vast majority of colon (80%) and breast (60%) tumors and sarcomas (73%) express CRD-BP whereas in other tumor types, for example prostate carcinomas, its expression is rare. CRD-BP expression has also been detected in benign tumors such as breast fibroadenomas, meningiomas and other benign mesenchymal tumors, implying a role for this gene in abnormal cell proliferation. In breast carcinomas, CRD-BP expression and or gene copy number gains in the region encompassing the c-myc locus were detected in approximately 75% of tumors. implying that the deregulated expression of c-myc may be more widespread than previously believed. Infiltrated lymph nodes, corresponding to CRD-BP- positive primary tumors, were also found positive indicating that monitoring for CRD-BP could prove useful for the detection and monitoring of disseminated disease.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 5
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