Goldberg Steven F, Miele Mary E, Hatta Naohito, Takata Minoru, Paquette-Straub Carrie, Freedman Leonard P, Welch Danny R
Jake Gittlen Cancer Research Institute, Penn State College of Medicine, Hershey, Pennsylvania 17033, USA.
Cancer Res. 2003 Jan 15;63(2):432-40.
Loss of genetic material on chromosome 6 has been associated with progression of human melanomas. We showed previously that introducing chromosome 6 into metastatic human melanoma cell lines suppresses metastasis without affecting the ability of the hybrids to form progressively growing tumors. By subtractive hybridization comparing nonmetastatic chromosome 6-containing (neo6/C8161) versus parental (C8161) metastatic cells, the KISS1 metastasis suppressor gene was isolated. However, KISS1 mapped to chromosome 1q32. To identify upstream regulator(s) of (and downstream effectors of) KISS1, microarray hybridization comparing C8161 and neo6/C8161 variants was performed. TXNIP/VDUP1, a thioredoxin-binding protein, was expressed more highly in neo6/C8161 and in nonmetastatic melanomas. Increased TXNIP expression inhibited metastasis and up-regulated KISS1. Surprisingly, TXNIP also mapped to chromosome 1q. PCR karyotyping that refined the region on chromosome 6 identified CRSP3/DRIP130, a transcriptional coactivator, as a metastasis suppressor. CRSP3 transfectant cells had up-regulated KISS1 and TXNIP expression and were suppressed for metastasis. Quantitative real-time reverse-transcription PCR of clinical melanoma samples showed that loss of CRSP3 expression correlated with decreased KISS1 expression and increased metastasis. Thus, we implicated a specific gene on chromosome 6 in the etiology of melanoma metastasis and identified potential up-stream regulators of KISS1 and TXNIP.
6号染色体上遗传物质的缺失与人类黑色素瘤的进展有关。我们之前表明,将6号染色体导入转移性人类黑色素瘤细胞系可抑制转移,而不影响杂种形成逐渐生长肿瘤的能力。通过消减杂交比较含非转移性6号染色体的(neo6/C8161)与亲本(C8161)转移性细胞,分离出了KISS1转移抑制基因。然而,KISS1定位于1号染色体1q32。为了鉴定KISS1的上游调节因子(和下游效应因子),进行了比较C8161和neo6/C8161变体的微阵列杂交。TXNIP/VDUP1,一种硫氧还蛋白结合蛋白,在neo6/C8161和非转移性黑色素瘤中表达更高。TXNIP表达增加抑制转移并上调KISS1。令人惊讶的是,TXNIP也定位于1号染色体1q。对6号染色体区域进行精细定位的PCR核型分析确定CRSP3/DRIP130,一种转录共激活因子,为转移抑制因子。CRSP3转染细胞中KISS1和TXNIP表达上调,转移受到抑制。临床黑色素瘤样本的定量实时逆转录PCR显示,CRSP3表达缺失与KISS1表达降低和转移增加相关。因此,我们发现黑色素瘤转移的病因与6号染色体上的一个特定基因有关,并鉴定出了KISS1和TXNIP的潜在上游调节因子。