School of Medicine, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
Department of Pathology, Show Chwan Memorial Hospital, Changhua City, Taiwan.
Sci Rep. 2021 Jun 9;11(1):12171. doi: 10.1038/s41598-021-91588-3.
Glycoprotein non-metastatic B (GPNMB) is a transmembrane protein overexpressed in numerous cancers including triple-negative breast cancers (TNBC). It has been linked to promote cancer aggressiveness and implicated as a novel target for GPNMB-expressing cancers. In current study, we aimed to explore the clinical significance of GPNMB in TNBC. Among 759 specimens, immunohistochemistry (IHC) exhibited GPNMB expressions were variable in different subtypes and significantly higher in TNBC. Kaplan-Meier analysis revealed GPNMB overexpression in TNBC was associated with worse prognosis especially distant metastasis (P = 0.020, HR = 2.515, CI 1.154-5.480). Multivariate analysis showed GPNMB expression was an independent prognostic factor in terms of recurrence and distant metastasis (P = 0.008, HR = 3.22, CI 1.36-7.61; P = 0.017, HR = 3.08, CI 1.22-7.74). In silico analysis showed high mRNA expression of GPNMB was associated with distant metastasis and GPNMB was overexpressed in TNBC. Furthermore, GPNMB positively correlated with epithelial-mesenchymal transition (EMT) regulators, mesenchymal marker vimentin, MMP and integrins. The protein levels of Twist and MMP2 were upregulated by GPNMB overexpression in TNBC cells. GPNMB-enhanced cell invasion was attenuated by broad spectrum MMP inhibitor (GM 6001) and the selective inhibitor of MMP-2 (ARP100). In summary, GPNMB expression is prevalent in TNBC and may be implicated as a prognostic biomarker in patients with TNBC.
糖蛋白非转移性 B(GPNMB)是一种跨膜蛋白,在许多癌症中过度表达,包括三阴性乳腺癌(TNBC)。它与促进癌症侵袭性有关,并被认为是表达 GPNMB 的癌症的一个新的治疗靶点。在本研究中,我们旨在探讨 GPNMB 在 TNBC 中的临床意义。在 759 例标本中,免疫组织化学(IHC)显示 GPNMB 的表达在不同亚型中存在差异,在 TNBC 中显著升高。Kaplan-Meier 分析显示,TNBC 中 GPNMB 的过表达与预后不良,特别是远处转移相关(P=0.020,HR=2.515,CI 1.154-5.480)。多变量分析显示,GPNMB 表达是复发和远处转移的独立预后因素(P=0.008,HR=3.22,CI 1.36-7.61;P=0.017,HR=3.08,CI 1.22-7.74)。计算机分析显示,GPNMB 的高 mRNA 表达与远处转移相关,GPNMB 在 TNBC 中过表达。此外,GPNMB 与上皮-间充质转化(EMT)调节因子、间充质标志物波形蛋白、MMP 和整合素呈正相关。在 TNBC 细胞中,GPNMB 过表达可上调 Twist 和 MMP2 的蛋白水平。GPNMB 增强的细胞侵袭可被广谱 MMP 抑制剂(GM 6001)和 MMP-2 的选择性抑制剂(ARP100)减弱。总之,GPNMB 的表达在 TNBC 中很常见,可能是 TNBC 患者的预后生物标志物。