Ohmura Gaku, Tsujikawa Takahiro, Yaguchi Tomonori, Kawamura Naoshi, Mikami Shuji, Sugiyama Juri, Nakamura Kenta, Kobayashi Asuka, Iwata Takashi, Nakano Hiroshi, Shimada Taketoshi, Hisa Yasuo, Kawakami Yutaka
Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan. Department of Otolaryngology-Head and Neck Surgery, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto City, Kyoto, Japan.
Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Mol Cancer Res. 2015 Apr;13(4):721-31. doi: 10.1158/1541-7786.MCR-14-0410. Epub 2014 Nov 24.
Lymph node metastasis is the major clinicopathologic feature associated with poor prognosis in patients with head and neck squamous cell carcinoma (HNSCC). Here, web-based bioinformatics meta-analysis was performed to elucidate the molecular mechanism of lymph node metastasis of human HNSCC. Preferential upregulation of Myosin 1b (MYO1B) transcript in HNSCC datasets was identified. Myo1b mRNA was highly expressed in human HNSCC cells and patient tissue specimens compared with their normal counterparts as shown by quantitative PCR (qPCR) analyses. Immunohistochemistry (IHC)-detected Myo1b expression was significantly correlated with lymph node metastases in patients with oral cancer of the tongue. HNSCC with high expression of Myo1b and chemokine receptor 4 (CCR4), another metastasis-associated molecule, was strongly associated with lymph node metastasis. RNA interference (RNAi) of Myo1b in HNSCC cells, SAS and HSC4, significantly inhibited migratory and invasive abilities through decreased large protrusion formation of cell membranes. Finally, Myo1b knockdown in SAS cells significantly inhibited in vivo cervical lymph node metastases in a cervical lymph node metastatic mouse model system.
Myo1b is functionally involved in lymph node metastasis of human HNSCC through enhanced cancer cell motility and is an attractive target for new diagnostic and therapeutic strategies for patients with HNSCC.
淋巴结转移是头颈部鳞状细胞癌(HNSCC)患者预后不良的主要临床病理特征。在此,进行了基于网络的生物信息学荟萃分析,以阐明人类HNSCC淋巴结转移的分子机制。在HNSCC数据集中发现肌球蛋白1b(MYO1B)转录本优先上调。定量PCR(qPCR)分析显示,与正常对照相比,Myo1b mRNA在人类HNSCC细胞和患者组织标本中高表达。免疫组织化学(IHC)检测到的Myo1b表达与舌部口腔癌患者的淋巴结转移显著相关。Myo1b和趋化因子受体4(CCR4,另一种与转移相关的分子)高表达的HNSCC与淋巴结转移密切相关。在HNSCC细胞SAS和HSC4中对Myo1b进行RNA干扰(RNAi),通过减少细胞膜大突起的形成,显著抑制了迁移和侵袭能力。最后,在宫颈淋巴结转移小鼠模型系统中,SAS细胞中Myo1b的敲低显著抑制了体内宫颈淋巴结转移。
Myo1b通过增强癌细胞运动性在人类HNSCC淋巴结转移中发挥功能作用,是HNSCC患者新诊断和治疗策略的一个有吸引力的靶点。