BNF-1, a novel gene encoding a putative extracellular matrix protein, is overexpressed in tumor tissues

被引:13
作者
Wu, IM
Moses, MA [1 ]
机构
[1] Harvard Univ, Sch Med, Childrens Hosp, Surg Res Lab, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Surg, Boston, MA 02115 USA
关键词
breast cancer; lung cancer; colon cancer; angiogenesis; cysteine-rich repeats;
D O I
10.1016/S0378-1119(03)00563-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In an effort to identify novel genes relevant to tumor angiogenesis, we compared the genes expressed in a matched pair composed of vascularized breast tumor and its adjacent normal tissue obtained from the same cancer patient. Using differential display, we identified a cDNA fragment that was reproducibly upregulated in vascularized breast tumor. Up-regulation of this gene fragment in vascularized breast tumor was further verified by semi-quantitative PCR on the same RNA pair using gene-specific primers. The cDNA encoding the full-length ORF of that gene was then cloned by both 3' and 5' RACE. Sequence analysis showed that this gene encodes an ORF of 1353 bp having a hydrophobic N-terminal signal sequence and a cleavage site. We named this novel gene BNF-1 (breast tumor novel factor 1). The mature protein of this gene contains cysteine-rich repeats that are a specific feature of several extracellular matrix proteins including thrombospondin-1. thrombospondin-2, pro-collagen type 1, and von Willebrand Factor 1. PCR analysis of BNF-1 expression in a variety of human adult normal tissues revealed that BNF-1 is expressed predominantly in liver, heart, prostate, testis, and ovary. To further study the expression pattern of this novel gene in tumor tissues, we extended our analysis to additional matched pairs of tumor tissues obtained from breast, lung. and colon cancer patients. We show here that BNF-1 is over-expressed not only in breast tumors but also in lung and colon tumors. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 110
页数:6
相关论文
共 19 条
  • [1] Antisense-mediated reduction in thrombospondin-1 expression reduces cell motility in malignant glioma cells
    Amagasaki, K
    Sasaki, A
    Kato, G
    Maeda, S
    Nukui, H
    Naganuma, H
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2001, 94 (04) : 508 - 512
  • [2] Role of Id proteins in embryonic and tumor angiogenesis
    Benezra, R
    [J]. TRENDS IN CARDIOVASCULAR MEDICINE, 2001, 11 (06) : 237 - 241
  • [3] Sp1 and kruppel-like factor family of transcription factors in cell growth regulation and cancer
    Black, AR
    Black, JD
    Azizkhan-Clifford, J
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 188 (02) : 143 - 160
  • [4] ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE
    FOLKMAN, J
    [J]. NATURE MEDICINE, 1995, 1 (01) : 27 - 31
  • [5] KLAGSBURN M, 1999, CHEM BIOL, V6, pR271
  • [6] LAHERTY CD, 1992, J BIOL CHEM, V267, P3274
  • [7] Luyten GPM, 1996, INT J CANCER, V66, P380, DOI 10.1002/(SICI)1097-0215(19960503)66:3<380::AID-IJC19>3.0.CO
  • [8] 2-F
  • [9] MIRAYLOPEZ R, 1990, CANCER RES, V50, P78
  • [10] CLONING A CDNA FOR THE PRO-ALPHA-2 CHAIN OF HUMAN TYPE-I COLLAGEN
    MYERS, JC
    CHU, ML
    FARO, SH
    CLARK, WJ
    PROCKOP, DJ
    RAMIREZ, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (06): : 3516 - 3520