Malpeli Giorgio, Filippini Federica, Tedone Fabrizio, Torroni Lorena, Alloggio Mariella, Castelli Claudia, Dal Cero Mariagiulia, Perris Roberto, Tomezzoli Anna, De Manzoni Giovanni, Bencivenga Maria
Department of Human Sciences for the Promotion of the Quality of Life, San Raffaele Roma Open University, 00166 Roma, Italy.
Unit of General and Upper GI Surgery, University of Verona, 37126 Verona, Italy.
J Pers Med. 2024 Feb 9;14(2):194. doi: 10.3390/jpm14020194.
Tumor-stroma crosstalk promotes the adaptation of cancer cells to the local microenvironment and sustains their growth. We assessed the quantitative and qualitative impact of intralesional stroma on clinic-pathological features and the prognosis of poorly cohesive gastric cancer (PCGC) variants. Tissue microarrays including 75 PCGC specimens were immunostained for cytokeratin 8/18 and α-smooth muscle actin to assess the relative proportion of neoplastic cells versus stromal components and the cases were subsequently divided into stroma-rich (SR) and stroma-poor (SP) tumors. Stromal status is significantly associated with the depth of tumor invasion. Patient survival rate was found to be higher in the SP compared to the SR tumor group and, hence, abundant stroma was identified as a significant risk factor in univariable analysis but had no independent prognostic impact. We also investigated the mRNA levels of KRT8 and the associated transcriptional signatures using the molecular data of 82 PCGC cases divided into KRT8-high and KRT8-low groups. KRT8-high tumors were enriched in proteins localized in the extracellular compartment and their expression levels correlated with longer survival in the KRT8-high group and shorter overall survival in the KRT8-low group. Comprehensively, we find that relative intralesional stromal content is a marker of aggressiveness in PCGC tumors and that extracellular proteins characterize functionally and clinically different PCGC subgroups.
肿瘤-基质相互作用促进癌细胞适应局部微环境并维持其生长。我们评估了瘤内基质对低黏附性胃癌(PCGC)变体的临床病理特征和预后的定量及定性影响。对包含75个PCGC标本的组织微阵列进行细胞角蛋白8/18和α-平滑肌肌动蛋白免疫染色,以评估肿瘤细胞与基质成分的相对比例,随后将病例分为基质丰富(SR)和基质贫乏(SP)肿瘤。基质状态与肿瘤浸润深度显著相关。发现SP肿瘤组的患者生存率高于SR肿瘤组,因此,在单变量分析中,丰富的基质被确定为一个显著的风险因素,但没有独立的预后影响。我们还使用82例PCGC病例的分子数据,将其分为KRT8高表达组和KRT8低表达组,研究了KRT8的mRNA水平及相关转录特征。KRT8高表达的肿瘤在细胞外区室定位的蛋白质中富集,其表达水平与KRT8高表达组的较长生存期和KRT8低表达组的较短总生存期相关。综合来看,我们发现瘤内相对基质含量是PCGC肿瘤侵袭性的一个标志物,并且细胞外蛋白质表征了功能和临床不同的PCGC亚组。