Smolle Elisabeth, Fink-Neuboeck Nicole, Lindenmann Joerg, Smolle-Juettner Freyja, Pichler Martin
Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria.
Department of Thoracic Surgery, Medical University of Graz, 8036 Graz, Austria.
Cancers (Basel). 2019 Aug 6;11(8):1118. doi: 10.3390/cancers11081118.
Carcinogenic mutations allow cells to escape governing mechanisms that commonly inhibit uncontrolled cell proliferation and maintain tightly regulated homeostasis between cell death and survival. Members of the inhibition of growth (ING) family act as tumor suppressors, governing cell cycle, apoptosis and cellular senescence. The molecular mechanism of action of genes, as well as their anchor points in pathways commonly linked to malignant transformation of cells, have been studied with respect to a variety of cancer specimens. This review of the current literature focuses specifically on the action mode of family members in lung cancer. We have summarized data from in vitro and in vivo studies, highlighting the effects of varying levels of expression in cancer cells. Based on the increasing insight into the function of these proteins, the use of family members as clinically useful biomarkers for lung cancer detection and prognosis will probably become routine in everyday clinical practice.
致癌性突变使细胞能够逃避通常抑制不受控制的细胞增殖并维持细胞死亡与存活之间严格调控的稳态的调控机制。生长抑制(ING)家族成员作为肿瘤抑制因子,调控细胞周期、细胞凋亡和细胞衰老。针对多种癌症标本,已经研究了这些基因的分子作用机制及其在通常与细胞恶性转化相关的通路中的锚定节点。本对当前文献的综述特别关注ING家族成员在肺癌中的作用模式。我们总结了来自体外和体内研究的数据,突出了癌细胞中ING不同表达水平的影响。基于对这些蛋白质功能的深入了解,将ING家族成员用作肺癌检测和预后的临床有用生物标志物可能会在日常临床实践中成为常规做法。