Literature DB >> 10049774

Cloning of BRAK, a novel divergent CXC chemokine preferentially expressed in normal versus malignant cells.

R Hromas1, H E Broxmeyer, C Kim, H Nakshatri, K Christopherson, M Azam, Y H Hou.   

Abstract

Chemokines are a family of related proteins that regulate leukocyte infiltration into inflamed tissue and play important roles in many disease processes. Chemokines are divided into two major groups, CC or CXC, based on their sequence around the amino terminal cysteines. We report the PCR cloning of a novel human chemokine termed BRAK for its initial isolation from breast and kidney cells. This novel chemokine is distantly related to other CXC chemokines (30% identity with MIP-2alpha and beta) and shares several biological activities. BRAK is expressed ubiquitously and highly in normal tissue. However, it was expressed in only 2 of 18 cancer cell lines. BRAK is located on human chromosome 5q31. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10049774     DOI: 10.1006/bbrc.1999.0257

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  66 in total

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3.  Chemokine CXCL14/BRAK transgenic mice suppress growth of carcinoma cell transplants. [corrected]

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Review 4.  Chemokines as mediators of angiogenesis.

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6.  Epigenetic silencing of CXCL14 induced colorectal cancer migration and invasion.

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7.  Inhibition of Myc-induced cell transformation by brain acid-soluble protein 1 (BASP1).

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Journal:  PLoS One       Date:  2010-04-23       Impact factor: 3.240

9.  Genome-wide analysis of gene expression in primate taste buds reveals links to diverse processes.

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10.  Differential gene expression in LPS/IFNgamma activated microglia and macrophages: in vitro versus in vivo.

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