Shin Min Sun, Kim Hong Sug, Lee Sug Hyung, Lee Jong Woo, Song Young Hwa, Kim Young Sill, Park Won Sang, Kim Su Young, Lee Shi Nae, Park Jik Young, Lee Jong Heun, Xiao Wensua, Jo Keon Hyon, Wang Young Pil, Lee Kyo Young, Park Yong Gyu, Kim Sang Ho, Lee Jung Young, Yoo Nam Jin
Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul 137-701, Korea.
Oncogene. 2002 Jun 13;21(26):4129-36. doi: 10.1038/sj.onc.1205527.
Many types of cancer cells are resistant to Fas-mediated apoptosis by several mechanisms, including the mutations of the genes involved in Fas-mediated apoptosis. In this study, to explore the possibility that the mutations of the genes involved in the proximal pathway of Fas-mediated apoptosis (Fas, FADD, caspase 8 and caspase 10) are involved in cancer metastasis, we have analysed somatic mutation and deletion of these genes in 80 non-small cell lung cancers (NSCLCs) with (n=43) and without (n=37) metastasis to the regional lymph nodes. We found 12 mutations (four Fas, four FADD, and four caspase 10 mutations) in 11 of 80 NSCLCs (13.8%). Interestingly, of these mutations, most mutations (10 out of 12) were detected in the NSCLCs with metastasis, and the frequency in the metastasis lesions (23%) was higher than that in the primary lesions of the NSCLCs without metastasis (5.4%). Furthermore, transfection study revealed that the tumor-derived mutants have decreased apoptosis inductions compared to the wild types. These data suggest that the inactivating mutations of the genes in the proximal pathway of Fas-mediated apoptosis may lead to a decreased cancer cell death and play a role in the metastasis of NSCLC.
多种类型的癌细胞可通过多种机制对Fas介导的凋亡产生抗性,包括参与Fas介导凋亡的基因突变。在本研究中,为了探究参与Fas介导凋亡近端途径(Fas、FADD、半胱天冬酶8和半胱天冬酶10)的基因突变是否与癌症转移有关,我们分析了80例非小细胞肺癌(NSCLC)中这些基因的体细胞突变和缺失情况,其中有区域淋巴结转移的为43例,无转移的为37例。我们在80例NSCLC中的11例(13.8%)中发现了12个突变(4个Fas突变、4个FADD突变和4个半胱天冬酶10突变)。有趣的是,在这些突变中,大多数突变(12个中的10个)在有转移的NSCLC中被检测到,且转移灶中的突变频率(23%)高于无转移的NSCLC原发灶中的频率(5.4%)。此外,转染研究表明,与野生型相比,肿瘤来源的突变体诱导凋亡的能力下降。这些数据表明,Fas介导凋亡近端途径中的基因失活突变可能导致癌细胞死亡减少,并在NSCLC转移中起作用。