RhoB is frequently downregulated in non-small-cell lung cancer and resides in the 2p24 homozygous deletion region of a lung cancer cell line

被引:43
作者
Sato, Naohito
Fukui, Takayuki
Taniguchi, Tetsuo
Yokoyama, Toshihiko
Kondo, Masashi
Nagasaka, Tetsuro
Goto, Yasuhiro
Gao, Wentao
Ueda, Yuichi
Yokoi, Kohei
Minna, John D.
Osada, Hirotaka
Kondo, Yutaka
Sekido, Yoshitaka
机构
[1] Aichi Canc Ctr, Res Inst, Div Mol Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Nagoya Univ, Dept Cardio Thorac Surg, Grad Sch Med, Nagoya, Aichi, Japan
[3] Nagoya Univ, Dept Resp Med, Grad Sch Med, Nagoya, Aichi, Japan
[4] Nagoya Univ, Sch Med, Dept Clin Pathol, Nagoya, Aichi 466, Japan
[5] Univ Texas, SW Med Ctr, Hamon Ctr Therapeut Oncol Res, Dallas, TX USA
关键词
RhoB; lung cancer; immunohistochemistry; homozygous deletion; chromosome; 2p;
D O I
10.1002/ijc.22328
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Identification of a homozygous deletion in cancer cells provides strong evidence for the location of a tumor suppressor gene (TSG). We analyzed the 2p24 homozygous deletion of a non-small-cell lung cancer (NSCLC) cell line, NCI-H2882, and found that the deletion size was 3.7 Mbp. Since RhoB, which has been suggested to be a candidate TSG, was located in this region, we analyzed RhoB for alterations in NSCLC. Although we found no mutations in 48 cell lines including 20 NSCLCs, a loss of heterozygosity (LOH) analysis in 128 primary NSCLCs showed that 25 of 62 informative samples had LOH at the RhoB locus. Northern blot analysis of 28 cell lines (including 15 NSCLCs) indicated that RhoB expression was downregulated in 27. We analyzed RhoB expression in 112 primary NSCLCs with immunohistochemistrv and found no or a weak RhoB expression in 33 (42%) of 78 adenocarcinomas, whereas we found it in 29 (94%) of 31 squamous cell carcinomas. No or a weak expression of RhoB was more frequently observed in poorly- or moderately-differentiated adenocarcinomas than in well-differentiated ones (p = 0.0014). Furthermore, no or a weak expression of RhoB indicated a tendency to poor patient prognosis. Although hypermethylation was not to found at the promoter region, the RhoB expression in NSCLC cell lines was induced by histone deacetylase inhibition, suggesting that RhoB downregulation may be due to histone modification. The present study demonstrates that RhoB expression is frequently downregulated in NSCLCs by multiple mechanisms, suggesting that RhoB is a candidate TSG or NSCLC. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:543 / 551
页数:9
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