Mardani Azam, Gheytanchi Elmira, Mousavie Seyed Hamzeh, Madjd Jabari Zahra, Shooshtarizadeh Tina
Department of Pathology, Iran University of Medical Science, Tehran, Iran.
Oncopathology Research Center, Iran University of Medical Science, Tehran, Iran.
Asian Pac J Cancer Prev. 2020 Jan 1;21(1):67-73. doi: 10.31557/APJCP.2020.21.1.67.
Osteosarcomas (OS) is one the most common primary bone malignancy in humans with the lungs metastasis in most cases. Metastasis and recurrence of OS is attributed to cancer stem cells (CSCs). Our study aimed to evaluate the clinical significance of CD133 and C-X-C chemokine receptor type 4 (CXCR4) as the frequently applied markers for CSCs in OS patients.
In this cross-sectional, a total of 50 tissue samples from the patients with primary OS were immunohistochemically examined to detect the expression of CD133 and CXCR4. The associations of the relative expression and clinical significance of each marker were also evaluated.
High level expression of CD133 was detected in 26% of OS patient tissues. Of the 12 patients who showed lung metastasis, 5 cases showed high expression of CD133 with marginal trend correlation (P=0.06). No significant correlation was observed between CD133 expression and clinicopathological factors. Only 36% of cases showed CXCR4 expression which was not significantly correlated with gender, age, tumor size, necrosis, stage and metastasis (P>0.05). Clinically, patients with concomitant CD133/CXCR4 expression had significant association with lung metastasis (P=0.05).
Our findings showed that concomitant expression of CSC markers CD133/CXCR4 might had a synergistic effect on the OS poor prognosis. These markers could be considered as potential therapeutic candidates of OS targeted therapy.
.
骨肉瘤(OS)是人类最常见的原发性骨恶性肿瘤,多数情况下会发生肺转移。骨肉瘤的转移和复发归因于癌症干细胞(CSCs)。我们的研究旨在评估CD133和C-X-C趋化因子受体4(CXCR4)作为骨肉瘤患者中常用的癌症干细胞标志物的临床意义。
在这项横断面研究中,对50例原发性骨肉瘤患者的组织样本进行免疫组织化学检查,以检测CD133和CXCR4的表达。还评估了每个标志物的相对表达与临床意义之间的关联。
在26%的骨肉瘤患者组织中检测到CD133的高水平表达。在12例出现肺转移的患者中,5例显示CD133高表达,具有边缘趋势相关性(P = 0.06)。未观察到CD133表达与临床病理因素之间存在显著相关性。仅36%的病例显示CXCR4表达,其与性别、年龄、肿瘤大小、坏死、分期和转移均无显著相关性(P>0.05)。临床上,同时表达CD133/CXCR4的患者与肺转移显著相关(P = 0.05)。
我们的研究结果表明,癌症干细胞标志物CD133/CXCR4的同时表达可能对骨肉瘤的不良预后具有协同作用。这些标志物可被视为骨肉瘤靶向治疗的潜在候选治疗靶点。