GBP-5 splicing variants:: New guanylate-binding proteins with tumor-associated expression and antigenicity

被引:43
作者
Fellenberg, F
Hartmann, TB
Dummer, R
Usener, D
Schadendorf, D
Eichmüller, S
机构
[1] German Canc Res Ctr, Dept D070, Skin Canc Unit, D-69120 Heidelberg, Germany
[2] Univ Spital Zurich, Dermatol Klin, Zurich, Switzerland
关键词
CTCL; GTPases; interferon; isoprenylation; melanoma; tumor immunology;
D O I
10.1111/j.0022-202X.2004.22613.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We have identified a new gene, gbp-5, with high homology to the guanylate binding proteins (GBP) belonging to the GTPase superfamily including the ras gene. gbp-5 is transcribed at least into three splicing variants (gbp-5a, -5b, and -5ta) leading to two different proteins (GBP-5a/b, GBP-5ta). GBP-5ta is C-terminally truncated by 97aa and has therefore lost its isoprenylation site. Although RT-PCR results indicated expression of GBP-5 members in selected normal tissues, western blotting using two newly generated antibodies revealed that expression of both proteins is restricted to peripheral blood monocytes with GBP-5ta at lower levels. In contrast, cutaneous T-cell lymphoma (CTCL) tumor tissues (seven of seven) were positive solely for GBP-5ta, and four of four CTCL cell lines expressed both proteins. Eight of nine melanoma cell lines expressed GBP-5a/b and four of nine additionally low levels of GBP-5ta. SEREX retesting using CTCL sera indicated a higher immunogenicity for GBP-5ta (nine of 16) than for GBP-5a/b (two of 11). Treatment of CTCL cell lines with interferon-gamma did not alter protein expression of GBP-5ta or GBP-5a/b. The restricted expression pattern of both GBP-5ta and GBP-5a/b and the pivotal role of many known members of the GTP-binding proteins in proliferation and differentiation suggest possible cancer-related functions of gbp-5.
引用
收藏
页码:1510 / 1517
页数:8
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