Wang Jinhua, Hua Wei, Huang Sharon K, Fan Kun, Takeshima Ling, Mao Ying, Hoon Dave S B
Department of Molecular Oncology, John Wayne Cancer Institute (JWCI), Providence Saint John's Health Center, Santa Monica, CA, USA.
Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Oncotarget. 2015 Oct 6;6(30):30165-77. doi: 10.18632/oncotarget.5030.
Our group previously demonstrated that the RASSF1 gene has a significant tumor suppressor role in cutaneous melanoma. The RASSF8 gene is a member of the N-terminal RASSF gene family. Previously, we identified RASSF8 (HOJ1, NCBI Gene ID:11228) expression in cutaneous melanoma; however the functional role of RASSF8 in melanoma is not known. RASSF8 expression was assessed in melanoma cell lines and tumors of different AJCC stages. Results indicated that RASSF8 expression was low in metastatic melanoma lines and decreased with melanoma progression. We then explored the mechanism of RASSF8 downregulation in melanoma by assessing methylation of RASSF8 and demonstrated that methylation of RASSF8 gene promoter was higher in advanced than in early stages melanomas. Functional activity of RASSF8 in melanoma lines by knockdown and overexpression of RASSF8 demonstrated that RASSF8 expression significantly inhibited cell growth, cell migration and invasion, whereas knockdown of RASSF8 expression significantly increased cell growth, cell migration and invasion of melanoma cells by increasing expression of P65 and its downstream target IL-6. Moreover RASSF8 was found to induce apoptosis in melanoma cells by activating the P53-P21 pathway, and also in vivo studies demonstrated that inhibiting RASSF8 increases the tumorigenic properties of human melanoma xenografts. These results suggest that RASSF8 plays a significant role in suppressing the progression of cutaneous melanoma.
我们的研究小组之前证明,RASSF1基因在皮肤黑色素瘤中具有显著的肿瘤抑制作用。RASSF8基因是N端RASSF基因家族的成员。此前,我们在皮肤黑色素瘤中鉴定出了RASSF8(HOJ1,NCBI基因ID:11228)的表达;然而,RASSF8在黑色素瘤中的功能作用尚不清楚。我们在黑色素瘤细胞系和不同AJCC分期的肿瘤中评估了RASSF8的表达。结果表明,RASSF8在转移性黑色素瘤细胞系中的表达较低,且随着黑色素瘤的进展而降低。然后,我们通过评估RASSF8的甲基化来探究黑色素瘤中RASSF8下调的机制,并证明RASSF8基因启动子的甲基化在晚期黑色素瘤中高于早期黑色素瘤。通过敲低和过表达RASSF8来研究其在黑色素瘤细胞系中的功能活性,结果表明,RASSF8的表达显著抑制细胞生长、细胞迁移和侵袭,而敲低RASSF8的表达则通过增加P65及其下游靶点IL-6的表达,显著增加黑色素瘤细胞的生长、细胞迁移和侵袭。此外,发现RASSF8通过激活P53-P21途径诱导黑色素瘤细胞凋亡,体内研究也表明,抑制RASSF8会增加人黑色素瘤异种移植物的致瘤特性。这些结果表明,RASSF8在抑制皮肤黑色素瘤的进展中起重要作用。