State Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology (Sichuan University), Chengdu, Sichuan 610041, P.R. China.
Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Provincial Cooperative Innovation Center of Industrial Fermentation, Hubei Key Laboratory of Industrial Microbiology, Hubei University of Technology, Wuhan, Hubei 430068, P.R. China.
Int J Oncol. 2019 Apr;54(4):1233-1244. doi: 10.3892/ijo.2019.4722. Epub 2019 Feb 22.
Cathepsin B (CTSB) has been reported to be involved in cancer metastasis by altering extracellular matrix (ECM) remodeling and facilitating invasion. However, the contribution of CTSB to collective cell invasion in salivary adenoid cystic carcinoma (SACC) and the underlying mechanisms remain unclear. The present study demonstrated that collective cell invasion is commonly observed in SACC without a complete epithelial‑mesenchymal transition signature. CTSB was found to be overexpressed in the invasive front of SACC compared to the tumor center, and was associated with a poor prognosis of patients with SACC. Subsequently, a 3D spheroid invasion assay was established in order to recapitulate the collective cell invasion of SACC and the results revealed that CTSB was only expressed in leader cells. The knockdown of CTSB by siRNA inhibited the migration and invasion of SACC‑83 cells and impaired the formation of leader cells. CTSB knockdown also disrupted cytoskeletal organization, altered cell morphology and inhibited ECM remodeling by downregulating matrix metalloproteinase‑9, focal adhesion kinase and Rho/ROCK function. Therefore, the present study provides evidence that CTSB may define leader cells in SACC and is required for collective cell invasion as a potential key regulator of ECM remodeling.
组织蛋白酶 B(CTSB)已被报道通过改变细胞外基质(ECM)重塑和促进侵袭参与癌症转移。然而,CTSB 对唾液腺腺样囊性癌(SACC)中细胞的集体侵袭的贡献及其潜在机制仍不清楚。本研究表明,在没有完全上皮-间充质转化特征的情况下,SACC 中经常观察到细胞的集体侵袭。与肿瘤中心相比,CTSB 在 SACC 的侵袭前缘中过表达,并且与 SACC 患者的不良预后相关。随后,建立了 3D 球体侵袭测定法以重现 SACC 的细胞的集体侵袭,结果表明 CTSB 仅在先导细胞中表达。siRNA 敲低 CTSB 抑制了 SACC-83 细胞的迁移和侵袭,并损害了先导细胞的形成。CTSB 敲低还破坏了细胞骨架组织,改变了细胞形态,并通过下调基质金属蛋白酶-9、黏着斑激酶和 Rho/ROCK 功能抑制 ECM 重塑。因此,本研究提供了证据表明 CTSB 可能在 SACC 中定义先导细胞,并且作为 ECM 重塑的潜在关键调节剂,需要用于细胞的集体侵袭。