López-Gómez M, Moreno-Rubio J, Suárez-García I, Cejas P, Madero R, Casado E, Jiménez A M, Sereno M, Gómez-Raposo C, Zambrana F, Merino M, Fernández-Luengas D, Feliu J
Medical Oncology Department, Infanta Sofía University Hospital, Paseo de Europa 34, San Sebastián de los Reyes, 28702, Madrid, Spain,
Clin Transl Oncol. 2015 Apr;17(4):322-9. doi: 10.1007/s12094-014-1233-3. Epub 2014 Oct 10.
Treatment of metastatic colorectal cancer (mCRC) is generally based on genetic testing performed in primary tumor biopsies, but whether the genomic status of primary tumors is identical to that of metastases is not well known. We compared the gene expression profiles of formalin-fixed paraffin-embedded (FFPE) biopsies of colorectal primary tumors and matched liver metastases.
We compared the expression of 18 genes in FFPE CRC tumors and their matched liver metastases from 32 patients. The expression of each gene in CRC primary tumors and their matched liver metastases was tested using Student's t test for paired samples. Pairwise correlations of each gene in the primary tumors and matched liver metastases were evaluated by Pearson's correlation coefficient.
The expression of six genes was significantly different in primary tumors compared with their matched liver metastases [CXCR4 (p < 0.001), THBS1 (p = 0.007), MMP 9 (p = 0.048), GST Pi (p = 0.050), TYMP (p = 0.042) and DPYD (p < 0.001)]. For the remaining genes, where no significant differences were observed, only SMAD4 (r s = 0.447, p = 0.010), ERCC1 (r s = 0.423, p = 0.016) and VEGF A (r s = 0.453, p = 0.009) showed significant correlation in expression between the two tissues. Therefore, we only detected similar gene expression levels between the tumor and the metastases in these three markers.
We only found similar gene expression levels between the tumor and the metastases in three genes (SMAD4, ERCC1, and VEGF A). However, our study could not assess whether the differences in gene expression were secondary to tumoral heterogeneity or to molecular changes induced by previous chemotherapy.
转移性结直肠癌(mCRC)的治疗通常基于原发肿瘤活检进行的基因检测,但原发肿瘤的基因组状态与转移灶是否相同尚不清楚。我们比较了结直肠癌原发肿瘤和配对肝转移灶的福尔马林固定石蜡包埋(FFPE)活检标本的基因表达谱。
我们比较了32例患者的FFPE结直肠癌肿瘤及其配对肝转移灶中18个基因的表达。使用配对样本的Student t检验检测结直肠癌原发肿瘤及其配对肝转移灶中每个基因的表达。通过Pearson相关系数评估原发肿瘤和配对肝转移灶中每个基因的成对相关性。
与配对肝转移灶相比,6个基因在原发肿瘤中的表达有显著差异[CXCR4(p < 0.001)、THBS1(p = 0.007)、MMP 9(p = 0.048)、GST Pi(p = 0.050)、TYMP(p = 0.042)和DPYD(p < 0.001)]。对于其余未观察到显著差异的基因,只有SMAD4(rs = 0.447,p = 0.010)、ERCC1(rs = 0.423,p = 0.016)和VEGF A(rs = 0.453,p = 0.009)在两种组织的表达之间显示出显著相关性。因此,我们仅在这三个标志物中检测到肿瘤与转移灶之间相似的基因表达水平。
我们仅在三个基因(SMAD4、ERCC1和VEGF A)中发现肿瘤与转移灶之间相似的基因表达水平。然而,我们的研究无法评估基因表达差异是继发于肿瘤异质性还是先前化疗诱导的分子变化。