Moschos S J, Smith A P, Mandic M, Athanassiou C, Watson-Hurst K, Jukic D M, Edington H D, Kirkwood J M, Becker D
Department of Medicine, University of Pittsburgh, Pittsburgh, PA 15213-1863, USA.
Oncogene. 2007 Jun 21;26(29):4216-25. doi: 10.1038/sj.onc.1210216. Epub 2007 Feb 12.
Although patients diagnosed with melanoma of </= 1.00 mm thickness have a relatively good cure rate, the prognosis for patients with locally advanced and metastatic melanoma is grave. The discovery of new and effective therapies for this disease depends in large part on molecular studies that will resolve why advanced-stage melanoma is refractory to conventional chemotherapy and radiation therapy. To identify genes that have important functions in advanced-stage melanomas, in particular, in melanoma-infiltrated lymph nodes, which are not well characterized at the molecular level, we generated a LongSAGE library from a melanoma-positive lymph node, and subjected melanoma-infiltrated lymph nodes to protein expression profiling. The data document that the molecular signature of melanoma, which has spread to regional lymph nodes, is very similar to the molecular signature of primary melanomas. Equally important, we provide evidence that the ubiquitin-conjugating enzyme, Ubc9, is expressed at high levels in melanoma-positive lymph nodes, and that it plays a crucial role in preventing advanced-stage melanomas from undergoing chemotherapy-induced apoptosis.
尽管被诊断为厚度≤1.00毫米的黑色素瘤患者的治愈率相对较高,但局部晚期和转移性黑色素瘤患者的预后却很严峻。针对这种疾病发现新的有效疗法在很大程度上依赖于分子研究,这些研究将揭示晚期黑色素瘤为何对传统化疗和放疗具有抗性。为了鉴定在晚期黑色素瘤中具有重要功能的基因,特别是在分子水平上尚未得到充分表征的黑色素瘤浸润淋巴结中,我们从一个黑色素瘤阳性淋巴结构建了一个长链寡核苷酸基因表达标签文库(LongSAGE文库),并对黑色素瘤浸润淋巴结进行了蛋白质表达谱分析。数据表明,已扩散至区域淋巴结的黑色素瘤的分子特征与原发性黑色素瘤的分子特征非常相似。同样重要的是,我们提供的证据表明,泛素缀合酶Ubc9在黑色素瘤阳性淋巴结中高水平表达,并且它在阻止晚期黑色素瘤发生化疗诱导的细胞凋亡中起关键作用。