Li Wan-Shan, Chen Chih-I, Chen Hsin-Pao, Liu Kuang-Wen, Tsai Chia-Jen, Yang Ching-Chieh
Institute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804, Taiwan.
Department of Pathology, Chi Mei Medical Center, Tainan 710, Taiwan.
Diagnostics (Basel). 2021 Nov 17;11(11):2132. doi: 10.3390/diagnostics11112132.
Data mining of a public transcriptomic rectal cancer dataset (GSE35452) from the Gene Expression Omnibus, National Center for Biotechnology Information identified the melanophilin () gene as the most significant intracellular protein transport-related gene (GO:0006886) associated with a poor response to preoperative chemoradiation. An MLPH immunostain was performed on biopsy specimens from 172 rectal cancer patients receiving preoperative chemoradiation; samples were divided into high- and low-expression groups by H-scores. Subsequently, the correlations between MLPH expression and clinicopathologic features, tumor regression grade, disease-specific survival (DSS), local recurrence-free survival (LRFS), and metastasis-free survival (MeFS) were analyzed. MLPH expression was significantly associated with CEA level ( = 0.001), pre-treatment tumor status ( = 0.022), post-treatment tumor status ( < 0.001), post-treatment nodal status ( < 0.001), vascular invasion ( = 0.028), and tumor regression grade ( < 0.001). After uni- and multi-variable analysis of five-year survival, MLPH expression was still associated with lower DSS (hazard ratio (HR), 10.110; 95% confidence interval (CI), 2.178-46.920; = 0.003) and MeFS (HR, 5.621; 95% CI, 1.762-17.931; = 0.004). In conclusion, identifying MLPH expression could help to predict the response to chemoradiation and survival, and aid in personal therapeutic modification.
对美国国立生物技术信息中心基因表达综合数据库中的一个公开的直肠癌转录组数据集(GSE35452)进行数据挖掘,确定亲黑素(MLPH)基因是与术前放化疗反应不佳相关的最显著的细胞内蛋白质转运相关基因(GO:0006886)。对172例接受术前放化疗的直肠癌患者的活检标本进行MLPH免疫染色;样本根据H评分分为高表达组和低表达组。随后,分析MLPH表达与临床病理特征、肿瘤退缩分级、疾病特异性生存(DSS)、无局部复发生存(LRFS)和无转移生存(MeFS)之间的相关性。MLPH表达与癌胚抗原水平(P = 0.001)、治疗前肿瘤状态(P = 0.022)、治疗后肿瘤状态(P < 0.001)、治疗后淋巴结状态(P < 0.001)、血管侵犯(P = 0.028)和肿瘤退缩分级(P < 0.001)显著相关。在对五年生存率进行单变量和多变量分析后,MLPH表达仍与较低的DSS(风险比(HR),10.110;95%置信区间(CI),2.178 - 46.920;P = 0.003)和MeFS(HR,5.621;95% CI,1.762 - 17.931;P = 0.004)相关。总之,识别MLPH表达有助于预测放化疗反应和生存情况,并有助于个性化治疗调整。