Tanaka Hisaaki, Yanagisawa Kiyoshi, Shinjo Keiko, Taguchi Ayumu, Maeno Ken, Tomida Shuta, Shimada Yukako, Osada Hirotaka, Kosaka Takayuki, Matsubara Hideo, Mitsudomi Tetsuya, Sekido Yoshitaka, Tanimoto Mitsune, Yatabe Yasushi, Takahashi Takashi
Division of Molecular Carcinogenesis, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Cancer Res. 2007 Jul 1;67(13):6007-11. doi: 10.1158/0008-5472.CAN-06-4774.
Emerging evidence, although currently very sparse, suggests the presence of "lineage-specific dependency" in the survival mechanisms of certain cancers. TTF-1 has a decisive role as a master regulatory transcription factor in lung development and in the maintenance of the functions of terminal respiratory unit (TRU) cells. We show that a subset of lung adenocarcinoma cell lines expressing TTF-1, which presumably represent those derived from the TRU lineage, exhibit marked dependence on the persistent expression of TTF-1. The inhibition of TTF-1 by RNA interference (RNAi) significantly and specifically induced growth inhibition and apoptosis in these adenocarcinoma cell lines. Furthermore, a fraction of TTF-1-expressing tumors and cell lines displayed an increase in the gene dosage of TTF-1 in the analysis of 214 patients with non-small-cell lung cancer, including 174 adenocarcinomas, showing a tendency of higher frequency of increased gene copies at metastatic sites than at primary sites (P=0.07, by two-sided Fisher's exact test). These findings strongly suggest that in addition to the development and maintenance of TRU lineages in normal lung, sustained TTF-1 expression may be crucial for the survival of a subset of adenocarcinomas that express TTF-1, providing credence for the lineage-specific dependency model.
尽管目前相关证据非常稀少,但新出现的证据表明,某些癌症的生存机制中存在“谱系特异性依赖性”。TTF-1作为主要调控转录因子,在肺发育以及终末呼吸单位(TRU)细胞功能维持中起决定性作用。我们发现,表达TTF-1的一部分肺腺癌细胞系(可能代表源自TRU谱系的细胞系)对TTF-1的持续表达表现出明显依赖性。通过RNA干扰(RNAi)抑制TTF-1可显著且特异性地诱导这些腺癌细胞系的生长抑制和凋亡。此外,在对214例非小细胞肺癌患者(包括174例腺癌患者)的分析中,一部分表达TTF-1的肿瘤和细胞系显示TTF-1基因剂量增加,且转移部位基因拷贝数增加的频率有高于原发部位的趋势(双侧Fisher精确检验,P = 0.07)。这些发现有力地表明,除了在正常肺中TRU谱系的发育和维持外,持续的TTF-1表达对于一部分表达TTF-1的腺癌的生存可能至关重要,这为谱系特异性依赖性模型提供了支持。