Ning Kai, Zhang Haoshaqiang, Wang Zhigang, Li Kun
Department of Orthopedics Surgery Center, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, People's Republic of China.
Onco Targets Ther. 2017 Feb 7;10:657-665. doi: 10.2147/OTT.S125418. eCollection 2017.
The Kindlin protein family, comprising Kindlin-1, Kindlin-2 and Kindlin-3, play important roles in various human cancers. Here, to explore the clinical significance of Kindlins in human osteosarcomas, quantitative real-time PCR and Western blot analyses were performed to detect the expression of Kindlin-1, Kindlin-2 and Kindlin-3 mRNAs and proteins in 20 self-pairs of osteosarcoma and adjacent noncancerous tissues. Then, immunohistochemistry was performed to examine subcellular localizations and expression patterns of Kindlin proteins in 100 osteosarcoma and matched adjacent noncancerous tissues. Kindlin-1, Kindlin-2 and Kindlin-3 protein immunostainings were localized in the cytoplasm, nucleus and cytoplasm, respectively, of tumor cells in primary osteosarcoma tissues. Statistically, the expression levels of Kindlin-1 and Kindlin-2 mRNAs and proteins in osteosarcoma tissues were all significantly higher (both <0.01), but those of Kindlin-3 mRNA and protein were both dramatically lower (both <0.05), than in matched adjacent noncancerous tissues. In addition, the overexpressions of Kindlin-1 and Kindlin-2 proteins were both significantly associated with high tumor grade (both =0.01), presence of metastasis (both =0.006), recurrence (both =0.006) and poor response to chemotherapy (both =0.02). Moreover, Kindlin-1 and Kindlin-2 expressions were both identified as independent prognostic factors for overall (both =0.01) and disease-free (=0.02 and 0.01, respectively) survivals of osteosarcoma patients. However, no associations were observed between Kindlin-3 expression and various clinicopathologic features and patients' prognosis. In conclusion, aberrant expression of Kindlin-1 and Kindlin-2 may function as reliable markers for progression and prognosis in osteosarcoma patients, especially for tumor recurrence.
包含Kindlin-1、Kindlin-2和Kindlin-3的Kindlin蛋白家族在多种人类癌症中发挥重要作用。在此,为探究Kindlins在人类骨肉瘤中的临床意义,进行了定量实时PCR和蛋白质印迹分析,以检测20对骨肉瘤及其相邻非癌组织中Kindlin-1、Kindlin-2和Kindlin-3 mRNA及蛋白质的表达。然后,进行免疫组织化学检测100例骨肉瘤及其配对的相邻非癌组织中Kindlin蛋白的亚细胞定位和表达模式。在原发性骨肉瘤组织中,Kindlin-1、Kindlin-2和Kindlin-3蛋白免疫染色分别定位于肿瘤细胞的细胞质、细胞核和细胞质。统计学分析显示,与配对的相邻非癌组织相比,骨肉瘤组织中Kindlin-1和Kindlin-2 mRNA及蛋白质的表达水平均显著更高(均<0.01),但Kindlin-3 mRNA和蛋白质的表达水平均显著更低(均<0.05)。此外,Kindlin-1和Kindlin-2蛋白的过表达均与高肿瘤分级(均=0.01)、转移的存在(均=0.006)、复发(均=0.006)以及对化疗反应不佳(均=0.02)显著相关。此外,Kindlin-1和Kindlin-2的表达均被确定为骨肉瘤患者总体生存(均=0.01)和无病生存(分别为=0.02和0.01)的独立预后因素。然而,未观察到Kindlin-3表达与各种临床病理特征及患者预后之间的关联。总之,Kindlin-1和Kindlin-2的异常表达可能作为骨肉瘤患者病情进展和预后的可靠标志物,尤其是对于肿瘤复发。