Waniczek D, Snietura M, Kopec A, Scieglinska D, Piglowski W, Lorenc Z, Muc-Wierzgon M, Nowakowska-Zajdel E
Department of Propaedeutics Surgery, Chair of General, Colorectal and Polytrauma Surgery, School of Health Sciences in Katowice, Medical University of Silesia, Katowice, Poland.
Tumor Pathology Department, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice Branch, Poland.
J Biol Regul Homeost Agents. 2016 Jan-Mar;30(1):79-90.
Phosphatase and Tensin Homolog deleted on chromosome 10 (PTEN) gene is one of the most important tumor suppressor genes which is involved in the regulation of many signaling cascades (AKT/PKB and MAPK). Subtle changes in its activity lead to cancer susceptibility or aggressive tumor behaviour. Despite the diversity of mechanisms leading to PTEN inactivation, it is frequently associated with a decreased or complete loss of protein expression. About 20% decrease in PTEN expression could lead to the development of cancer. There have been no objective, quantitative methods of PTEN expression assessment that allow to measure the subtle variations of the protein concentration in a tissue-contextual manner. A new quantitative algorithm of immunostaining evaluation based on combination of color deconvolution and relative chromogen signal intensity was used in the study. The proposed algorithm was implemented in the popular ImageJ image analysis software and positively verified in cancer cell lines and tissue models as well as in the tissue samples of colorectal cancer (CRC) patients. The proposed quantitative method of PTEN expression assessment creates an alternative to currently available subjective methods and forms the basis for inter-case and inter-tissue comparisons. Using the algorithm it would be possible to identify three groups of patients with advanced colorectal cancer which could significantly differ in the overall survival. The research should be continued.
10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)基因是最重要的肿瘤抑制基因之一,它参与许多信号级联反应(AKT/PKB和MAPK)的调控。其活性的细微变化会导致癌症易感性或肿瘤侵袭性行为。尽管导致PTEN失活的机制多种多样,但它常常与蛋白质表达的降低或完全丧失有关。PTEN表达下降约20%可能导致癌症的发生。目前还没有客观、定量的PTEN表达评估方法能够以组织背景的方式测量蛋白质浓度的细微变化。本研究使用了一种基于颜色反卷积和相对显色信号强度相结合的免疫染色评估新定量算法。所提出的算法在流行的ImageJ图像分析软件中实现,并在癌细胞系、组织模型以及结直肠癌(CRC)患者的组织样本中得到了积极验证。所提出的PTEN表达评估定量方法为目前可用的主观方法提供了一种替代方案,并为病例间和组织间比较奠定了基础。使用该算法有可能识别出三组晚期结直肠癌患者,他们的总生存率可能存在显著差异。该研究应继续进行。