Alterations of Fas-pathway genes associated with nodal metastasis in non-small cell lung cancer

被引:59
作者
Shin, MS
Kim, HS
Lee, SH
Lee, JW
Song, YH
Kim, YS
Park, WS
Kim, SY
Lee, SN
Park, JY
Lee, JH
Xiao, WS
Jo, KH
Wang, YP
Lee, KY
Park, YG
Kim, SH
Lee, JY
Yoo, NJ [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Pathol, Seoul 137701, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Thorac Surg, Seoul 137701, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Clin Pathol, Seoul 137701, South Korea
[4] Catholic Univ Korea, Coll Med, Dept Biostat, Seoul 137701, South Korea
关键词
Fas; FADD; caspase; 10; lung cancer; metastasis;
D O I
10.1038/sj.onc.1205527
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4129 / 4136
页数:8
相关论文
共 21 条
[11]  
Lee SH, 1999, CANCER RES, V59, P3068
[12]  
LEITHAUSER F, 1993, LAB INVEST, V69, P415
[13]   Fas gene mutation in the progression of adult T cell leukemia [J].
Maeda, T ;
Yamada, Y ;
Moriuchi, R ;
Sugahara, K ;
Tsuruda, K ;
Joh, T ;
Atogami, S ;
Tsukasaki, K ;
Tomonaga, M ;
Kamihira, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (07) :1063-1071
[14]   A CASP-8 mutation recognized by cytolytic T lymphocytes on a human head and neck carcinoma [J].
Mandruzzato, S ;
Brasseur, F ;
Andry, G ;
Boon, T ;
vanderBruggen, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (05) :785-793
[15]   Apoptosis by death factor [J].
Nagata, S .
CELL, 1997, 88 (03) :355-365
[16]  
NATOLI G, 1995, ONCOGENE, V11, P1157
[17]   Fas and fas ligand interactions suppress melanoma lung metastasis [J].
Owen-Schaub, LB ;
van Golen, KL ;
Hill, LL ;
Price, JE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (09) :1717-1723
[18]  
Petersen S, 2000, BRIT J CANCER, V82, P65
[19]  
Shin MS, 2001, CANCER RES, V61, P4942
[20]   Alterations of Fas (Apo-1/CD95) gene in cutaneous malignant melanoma [J].
Shin, MS ;
Park, WS ;
Kim, SY ;
Kim, HS ;
Kang, SJ ;
Song, KY ;
Park, JY ;
Dong, SM ;
Pi, JH ;
Oh, RR ;
Lee, JY ;
Yoo, NJ ;
Lee, SH .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (06) :1785-1791