| RB1CC1 suppresses cell cycle progression through RB1 expression in human neoplastic cells. | |
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MedLine Citation:
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PMID: 14533007 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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RB1-inducible Coiled-Coil 1 (RB1CC1) is a putative transcription factor that functions as a key regulator of retinoblastoma 1 (RB1). RB1CC1 mutations lacking this function are involved in the tumorigenesis of breast cancers. RB1CC1 is distributed in various tissues other than the breast, and is thought to play a biological role in controlling cell growth and progression of various cancers. The present study examined the correlation between RB1CC1 and cell cycle-related molecules in human neoplastic cells, and the ratios of cells at various phases of the cell cycle were verified in the RB1CC1-transduced human leukemic cell lines, K562 and Jurkat. The results showed that RB1CC1 was synchronously expressed with RB1 in various cell lines and that introducing RB1CC1 induced RB1 expression in human leukemic cell lines, although independently of the other molecules. Western blotting showed that underphosphorylated forms of RB1 were elicited by RB1CC1, whereas E2F1 was not affected. Cell cycle analysis demonstrated that G2-M phases were suppressed in RB1CC1-transduced cells. These data suggested that RB1CC1 induces the expression of RB1, especially of underphosphorylated forms, then suppresses cell cycle progression in human neoplastic cells. |
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Authors:
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Keiichi Kontani; Tokuhiro Chano; Yoshitomo Ozaki; Noriaki Tezuka; Satoru Sawai; Shozo Fujino; Yukikazu Saeki; Hidetoshi Okabe |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: International journal of molecular medicine Volume: 12 ISSN: 1107-3756 ISO Abbreviation: Int. J. Mol. Med. Publication Date: 2003 Nov |
Date Detail:
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Created Date: 2003-10-08 Completed Date: 2004-07-28 Revised Date: 2009-11-19 |
Medline Journal Info:
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Nlm Unique ID: 9810955 Medline TA: Int J Mol Med Country: Greece |
Other Details:
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Languages: eng Pagination: 767-9 Citation Subset: IM |
Affiliation:
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Department of Surgery, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Cell Cycle* Female G2 Phase Humans Mitosis Protein-Tyrosine Kinases / genetics, metabolism* RNA, Messenger / genetics, metabolism Retinoblastoma Protein / genetics, metabolism* Reverse Transcriptase Polymerase Chain Reaction Tumor Cells, Cultured |
| Chemical | |
Reg. No./Substance:
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0/RNA, Messenger; 0/Retinoblastoma Protein; EC 2.7.1.-/RB1CC1 protein, human; EC 2.7.10.1/Protein-Tyrosine Kinases |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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