Department of Pathology, Tianjin Cancer Hospital, Tianjin Medical University, Tianjin, China.
J Surg Oncol. 2013 Nov;108(6):414-9. doi: 10.1002/jso.23402. Epub 2013 Aug 29.
The aim of this study was to investigate the clinical significances and prognostic value of CD133 and CD44 (markers of cancer stem-like cells, CSCs), and vasculogenic mimicry (VM) in renal cell carcinoma (RCC).
Immunohistochemistry was performed to detect CD133 and CD44 expression and VM in 110 RCC patients proven to exhibit de novo metastases after radical nephrectomy.
In RCC, positive rates of 27.3%, 20.9%, and 21.8% were obtained for CD44, CD133, and VM, respectively. CD44 was significantly associated with tumor size, grade, stage, and histological type. CD44 expression may serve as a predictor of the number of metastases sites in RCC. CD133 expression correlated with tumor grade, stage, histological type, and tumor location. VM was positively associated with tumor grade and stage. Microvessel density (MVD) positively corresponded to tumor size, grade, and stage. CD133 expression was not associated with MVD, but significantly correlated with VM. CD44 expression correlated marginally with VM, but was found to have a significantly association with MVD. A close relationship between CSCs, MVD, and VM was established. The overall survival times of patients with CD133-high positive, CD44-high positive, VM-positive, and MVD <43 were lower than that of the patients with low positive, negative, and MVD ≥43. Tumor grade and presence of VM were independent prognostic factors of RCC.
Findings show that higher CSCs and VM was correlated with more aggressive clinicopathologic. VM was an independent unfavorable prognostic factor. The authors consistently observed that CSCs may be related to angiogenesis and vasculogenic mimicry.
本研究旨在探讨 CD133 和 CD44(癌症干细胞样细胞标志物,CSCs)和血管生成拟态(VM)在肾细胞癌(RCC)中的临床意义和预后价值。
对 110 例经根治性肾切除术后证实有新发转移的 RCC 患者进行免疫组织化学检测 CD133 和 CD44 表达及 VM。
在 RCC 中,CD44、CD133 和 VM 的阳性率分别为 27.3%、20.9%和 21.8%。CD44 与肿瘤大小、分级、分期和组织学类型显著相关。CD44 表达可能是 RCC 转移部位数量的预测因子。CD133 表达与肿瘤分级、分期、组织学类型和肿瘤位置相关。VM 与肿瘤分级和分期呈正相关。微血管密度(MVD)与肿瘤大小、分级和分期呈正相关。CD133 表达与 MVD 无相关性,但与 VM 显著相关。CD44 表达与 VM 呈弱相关,但与 MVD 有显著相关性。CSCs、MVD 和 VM 之间存在密切关系。CD133 高阳性、CD44 高阳性、VM 阳性和 MVD<43 的患者总生存时间低于 CD133 低阳性、CD44 阴性和 MVD≥43 的患者。肿瘤分级和 VM 的存在是 RCC 的独立预后因素。
研究结果表明,较高的 CSCs 和 VM 与更具侵袭性的临床病理特征相关。VM 是独立的不良预后因素。作者一致观察到 CSCs 可能与血管生成和血管生成拟态有关。