Saloura Vassiliki, Vougiouklakis Theodore, Zewde Makda, Kiyotani Kazuma, Park Jae-Hyun, Gao Guimin, Karrison Theodore, Lingen Mark, Nakamura Yusuke, Hamamoto Ryuji
Department of Medicine, University of Chicago, Chicago, IL, USA.
Department of Public Health Sciences, University of Chicago, Chicago, IL, USA.
Oncotarget. 2016 Jul 5;7(27):42527-42538. doi: 10.18632/oncotarget.9897.
Wolf-Hisrchhorn Syndrome Candidate 1-Like 1 (WHSC1L1) is a protein lysine methyltransferase that is recurrently amplified (8p11.23) in patients with squamous cell carcinoma of the head and neck (SCCHN). In this study, we investigated the oncogenic role of WHSC1L1 in SCCHN. Using immunohistochemistry on tissue microarrays of patients with locoregionally advanced SCCHN, we found that WHSC1L1 is significantly overexpressed in patients with SCCHN, and is associated with poor grade and heavy smoking history. Knockdown of WHSC1L1 expression resulted in significant growth suppression and reduction of H3K36 dimethylation (H3K36me2) in SCCHN cells. Chromatin immunoprecipitation analysis showed that WHSC1L1 and H3K36me2 are enriched in the gene bodies of the cell cycle-related genes CDC6 and CDK2, implying that WHSC1L1 directly regulates the transcription of these genes. According to the importance of CDC6 and CDK2 for G1 to S transition, WHSC1L1 knockdown induced strong G0/G1 arrest which was rescued by introduction of wild-type WHSC1L1 but not by that of enzyme-inactive WHSC1L1. Our results imply that WHSC1L1 and its product H3K36me2 are essential for the transition from G1 to S phase in SCCHN cells and that WHSC1L1 could serve as a rational target for anticancer drug development for patients with head and neck cancer.
狼-希氏综合征候选基因1样蛋白1(WHSC1L1)是一种蛋白质赖氨酸甲基转移酶,在头颈部鳞状细胞癌(SCCHN)患者中经常发生扩增(8p11.23)。在本研究中,我们调查了WHSC1L1在SCCHN中的致癌作用。通过对局部晚期SCCHN患者的组织微阵列进行免疫组织化学分析,我们发现WHSC1L1在SCCHN患者中显著过表达,并且与低分化和重度吸烟史相关。敲低WHSC1L1的表达导致SCCHN细胞的显著生长抑制和H3K36二甲基化(H3K36me2)的减少。染色质免疫沉淀分析表明,WHSC1L1和H3K36me2在细胞周期相关基因CDC6和CDK2的基因体内富集,这意味着WHSC1L1直接调节这些基因的转录。根据CDC6和CDK2对G1期到S期转变的重要性,敲低WHSC1L1诱导强烈的G0/G1期阻滞,野生型WHSC1L1的导入可挽救这种阻滞,但酶失活的WHSC1L1则不能。我们的结果表明,WHSC1L1及其产物H3K36me2对于SCCHN细胞从G1期到S期的转变至关重要,并且WHSC1L1可以作为头颈癌患者抗癌药物开发的合理靶点。