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

被引:164
作者
Hromas, R
Broxmeyer, HE
Kim, C
Nakshatri, H
Christopherson, K
Azam, M
Hou, YH
机构
[1] Indiana Univ, Med Ctr, Dept Hematol & Oncol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Med Ctr, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Med Ctr, Walther Oncol Ctr, Indianapolis, IN 46202 USA
[4] Indiana Univ, Med Ctr, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[5] Expressgen, Chicago, IL 60612 USA
关键词
D O I
10.1006/bbrc.1999.0257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-2 alpha 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. (C) 1999 Academic Press.
引用
收藏
页码:703 / 706
页数:4
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