Kita Akihiro, Kasamatsu Atsushi, Nakashima Dai, Endo-Sakamoto Yosuke, Ishida Sho, Shimizu Toshihiro, Kimura Yasushi, Miyamoto Isao, Yoshimura Shusaku, Shiiba Masashi, Tanzawa Hideki, Uzawa Katsuhiro
Department of Oral Science, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8670, Japan.
Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, 1-8-1 Inohana, Chuo-ku, Chiba 260-8670, Japan.
J Cancer. 2017 Jul 5;8(11):2033-2041. doi: 10.7150/jca.18714. eCollection 2017.
Activin B, a homodimer of inhibin beta b (INHBB), is a multifunctional cytokine belonging to the transforming growth factor-β (TGF-β) family. However, the molecular functions and clinical relevance of activin B have not been determined in oral cancer. We investigated the critical roles of activin B in oral squamous cell carcinoma (OSCC). We performed quantitative reverse transcriptase-polymerase chain reaction, Western blotting, and immunohistochemistry to study INHBB expression in OSCC-derived cell lines and OSCC clinical samples. The INHBB expression levels were significantly (P < 0.05) overexpressed in OSCCs compared to normal counterparts and . Activin B-positivity in OSCC cases was significantly (P < 0.05) correlated with regional lymph node metastasis. The INHBB knockdown (shINHBB) cells promoted cellular adhesion and suppression of cellular invasiveness and migration. After treatment of shINHBB cells with activin B, those activities were restored similar to the shMock cells. In the processes of invasiveness and metastasis, the cells cause epithelial-mesenchymal transition (EMT). TGF-β and its family members are promoters of the EMT process. To investigate whether activin B is related to EMT, we examined the expressions of EMT-related genes and found that INHBB was related closely to EMT. Our results suggested for the first time that activin B indicates tumoral metastasis in OSCCs and might be a useful biomarker for OSCC metastasis.
激活素B是抑制素βb(INHBB)的同二聚体,是一种属于转化生长因子-β(TGF-β)家族的多功能细胞因子。然而,激活素B在口腔癌中的分子功能和临床相关性尚未确定。我们研究了激活素B在口腔鳞状细胞癌(OSCC)中的关键作用。我们进行了定量逆转录聚合酶链反应、蛋白质免疫印迹和免疫组织化学,以研究INHBB在OSCC来源的细胞系和OSCC临床样本中的表达。与正常对照相比,OSCC中INHBB的表达水平显著(P < 0.05)上调。OSCC病例中的激活素B阳性与区域淋巴结转移显著(P < 0.05)相关。INHBB基因敲低(shINHBB)细胞促进细胞黏附,并抑制细胞侵袭和迁移。用激活素B处理shINHBB细胞后,这些活性恢复到与shMock细胞相似的水平。在侵袭和转移过程中,细胞会发生上皮-间质转化(EMT)。TGF-β及其家族成员是EMT过程的促进因子。为了研究激活素B是否与EMT相关,我们检测了EMT相关基因的表达,发现INHBB与EMT密切相关。我们的结果首次表明,激活素B在OSCC中提示肿瘤转移,可能是OSCC转移的一个有用生物标志物。