Zhang Mei, Wu Jia-Shun, Yang Xiao, Pang Xin, Li Li, Wang Sha-Sha, Wu Jing-Biao, Tang Ya-Jie, Liang Xin-Hua, Zheng Min, Tang Ya-Ling
State Key Laboratory of Oral Disease, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Front Oncol. 2018 Oct 31;8:492. doi: 10.3389/fonc.2018.00492. eCollection 2018.
Cathepsin D (CTSD) is a pivotal orchestrator in the occurrence and development of tumors. Recently, CTSD was detected in salivary adenoid cystic carcinoma (SACC). However, its functional role in perineural invasion (PNI) of SACC remained elusive. We conducted the present study to detect the expression of CTSD in SACC, analyze the correlation between CTSD expression and prognosis of SACC patients and elucidate the role of CTSD in occurrence of PNI in SACC to lay the foundation for further studies. Immunohistochemical analysis was conducted to assess CTSD and Ki67 expression in 158 SACC samples and 20 normal salivary gland samples adjacent to carcinoma. Meanwhile, the correlation between CTSD and PNI of SACC specimens was analyzed using Wilcoxon test. QRT-PCR, immunofluorescence and western blot analysis were used to examine the levels of CTSD mRNA and protein in SACC-LM cell line. SiRNA-mediated CTSD silence was performed. Scratch wound healing assay, transwell invasion assay and DRG co-culture assay of PNI was used to detect the ability of migration, invasion and PNI. FITC-phalloidin was used to detect cytoskeletal organization. Our data demonstrated that the positive expression of CTSD was observed in 74.1% (117/158) of SACC cases, and the expression of CTSD was significantly correlated with the PNI ( < 0.05). The ability of migration, invasion, and PNI could be inhibited significantly by siRNA-mediated CTSD silence ( < 0.01). Furthermore, siRNA-mediated CTSD silence inhibited cytoskeletal organization and pseudo foot formation in SACC-LM cells. Our results suggested that an association between PNI and expression of CTSD existed. CTSD may promote PNI of SACC accompanied by cytoskeletal organization and pseudo foot formation.
组织蛋白酶D(CTSD)是肿瘤发生发展过程中的关键调控因子。最近,在涎腺腺样囊性癌(SACC)中检测到了CTSD。然而,其在SACC神经周侵犯(PNI)中的功能作用仍不清楚。我们开展本研究以检测CTSD在SACC中的表达,分析CTSD表达与SACC患者预后的相关性,并阐明CTSD在SACC发生PNI中的作用,为进一步研究奠定基础。对158例SACC样本和20例癌旁正常涎腺样本进行免疫组化分析,以评估CTSD和Ki67的表达。同时,采用Wilcoxon检验分析SACC标本中CTSD与PNI的相关性。运用QRT-PCR、免疫荧光和蛋白质印迹分析检测SACC-LM细胞系中CTSD mRNA和蛋白质水平。进行siRNA介导的CTSD沉默。采用划痕伤口愈合试验、Transwell侵袭试验和PNI的背根神经节共培养试验检测迁移、侵袭和PNI能力。使用FITC-鬼笔环肽检测细胞骨架组织。我们的数据表明,74.1%(117/158)的SACC病例中观察到CTSD阳性表达,且CTSD表达与PNI显著相关(<0.05)。siRNA介导的CTSD沉默可显著抑制迁移、侵袭和PNI能力(<0.01)。此外,siRNA介导的CTSD沉默抑制了SACC-LM细胞中的细胞骨架组织和伪足形成。我们的结果提示PNI与CTSD表达之间存在关联。CTSD可能通过细胞骨架组织和伪足形成促进SACC的PNI。