Popiel-Kopaczyk Aneta, Grzegrzolka Jedrzej, Piotrowska Aleksandra, Olbromski Mateusz, Smolarz Beata, Romanowicz Hanna, Rusak Agnieszka, Mrozowska Monika, Dziegiel Piotr, Podhorska-Okolow Marzenna, Kobierzycki Christopher
Division of Histology and Embryology, Department of Human Morphology and Embryology, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Department of Pathology, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.
Curr Issues Mol Biol. 2023 Jan 5;45(1):490-500. doi: 10.3390/cimb45010032.
Testin is a protein expressed in normal human tissues, being responsible, with other cytoskeleton proteins, for the proper functioning of cell−cell junction areas and focal adhesion plaques. It takes part in the regulation of actin filament changes during cell spreading and motility. Loss of heterozygosity in the testin-encoding gene results in altered protein expression in many malignancies, as partly described for cervical cancer. The aim of our study was the assessment of the immunohistochemical (IHC) expression of testin in cervical cancer and its analysis in regard to clinical data as well the expression of the Ki-67 antigen and p16 protein. Moreover, testin expression was assessed by Western blot (WB) in commercially available cell lines. The IHC analysis disclosed that the expression of testin inversely correlated with p16 (r = −0.2104, p < 0.0465) and Ki-67 expression (r = −0.2359, p < 0.0278). Moreover, weaker testin expression was observed in cancer cases vs. control ones (p < 0.0113). The WB analysis of testin expression in the cervical cancer cell lines corresponded to the IHC results and showed a weaker expression compared to that in the control cell line. When we compared the expression of testin in cervical cancer cell lines, we found a weaker expression in HPV-negative cell lines. In summary, we found that the intensity of testin expression and the number of positive cells inversely correlated with the expression of Ki-67 (a marker of proliferation) and p16 (a marker of cell cycle dysregulation). This study shows that the combined assessment of testin, Ki-67 and p16 expression may improve cervical cancer diagnostics.
Testin是一种在正常人体组织中表达的蛋白质,它与其他细胞骨架蛋白共同负责细胞间连接区域和粘着斑的正常功能。它参与细胞铺展和运动过程中肌动蛋白丝变化的调节。编码Testin的基因杂合性缺失会导致许多恶性肿瘤中蛋白质表达改变,宫颈癌部分情况已有所描述。我们研究的目的是评估Testin在宫颈癌中的免疫组织化学(IHC)表达,并结合临床数据以及Ki-67抗原和p16蛋白的表达进行分析。此外,通过蛋白质免疫印迹法(WB)对市售细胞系中的Testin表达进行了评估。免疫组织化学分析显示,Testin的表达与p16(r = -0.2104,p < 0.0465)和Ki-67表达(r = -0.2359,p < 0.0278)呈负相关。此外,与对照组相比,癌症病例中Testin表达较弱(p < 0.0113)。对宫颈癌细胞系中Testin表达的蛋白质免疫印迹分析结果与免疫组织化学结果一致,且与对照细胞系相比表达较弱。当我们比较宫颈癌细胞系中Testin的表达时,发现HPV阴性细胞系中的表达较弱。总之,我们发现Testin表达的强度和阳性细胞数量与Ki-67(增殖标志物)和p16(细胞周期失调标志物)的表达呈负相关。这项研究表明,联合评估Testin、Ki-67和p16的表达可能会改善宫颈癌的诊断。