Buck Emanuel, Sprick Martin, Gaida Matthias M, Grüllich Carsten, Weber Tim Frederik, Herpel Esther, Bruckner Thomas, Koschny Ronald
Department of Gastroenterology, University Hospital Heidelberg, D-69120 Heidelberg, Germany.
HI-STEM gGmbH/German Cancer Research Center Heidelberg (MRS), D-69120 Heidelberg, Germany.
Oncol Lett. 2019 Apr;17(4):3890-3898. doi: 10.3892/ol.2019.10043. Epub 2019 Feb 14.
Recently, a tumor-autonomous cytochrome P450 (CYP)-3A5-mediated resistance to cancer therapy has been demonstrated in pancreatic ductal adenocarcinoma. Expression of CYP3A5, which is involved in the degradation of irinotecan, has also been reported in colorectal cancer (CRC). The aim of the present study was to analyze CYP3A5 expression in the normal colon, colon adenoma, CRC and normal tissues, as well as to examine whether CYP3A5 expression in CRC has an impact on tumor response to irinotecan treatment. Immunohistochemistry was used to assess 85 tissue samples from 65 patients with CRC, along with 15 samples of normal colon and 45 samples of colon adenoma (including tubular, tubulovillous, and sessile serrated adenomas), and a tissue microarray (TMA) comprised of 26 different normal tissue types. Expression of CYP3A5 was evaluated with a semi-quantitative score. Tumor response to irinotecan therapy was assessed according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 guidelines. In normal tissues, CYP3A5 was expressed in epithelial cells of the colon, gallbladder, kidney, liver, small intestine, stomach, thyroid gland and tonsil, as well as in nerves. Expression in colon mucosa was heterogeneous, with only weak staining in the minority of specimens. CYP3A5 exhibited markedly higher expression in adenomas compared with normal colon tissues. A statistically significant inverse correlation was identified between CYP3A5 expression in CRC tissues and tumor response to irinotecan therapy. Irinotecan treatment itself did not alter CYP3A5 expression in CRC tissues. As CYP3A5 is involved in the degradation of irinotecan, the significantly higher intratumoral expression of CYP3A5 in patients with CRC who do not respond to irinotecan-based chemotherapy may indicate a causal role of CYP3A5 in tumor resistance.
最近,在胰腺导管腺癌中已证实一种肿瘤自主性细胞色素P450(CYP)-3A5介导的癌症治疗耐药性。参与伊立替康降解的CYP3A5在结直肠癌(CRC)中也有表达。本研究的目的是分析CYP3A5在正常结肠、结肠腺瘤、CRC及正常组织中的表达情况,并探讨CRC中CYP3A5表达是否对肿瘤对伊立替康治疗的反应有影响。采用免疫组织化学方法评估65例CRC患者的85份组织样本,以及15份正常结肠样本和45份结肠腺瘤样本(包括管状、管状绒毛状和无蒂锯齿状腺瘤),还有一个由26种不同正常组织类型组成的组织芯片(TMA)。用半定量评分评估CYP3A5的表达。根据实体瘤疗效评价标准(RECIST)1.1指南评估肿瘤对伊立替康治疗的反应。在正常组织中,CYP3A5在结肠、胆囊、肾脏、肝脏、小肠、胃、甲状腺和扁桃体的上皮细胞以及神经中表达。结肠黏膜中的表达是异质性的,少数标本仅有弱阳性染色。与正常结肠组织相比,CYP3A5在腺瘤中的表达明显更高。在CRC组织中CYP3A5表达与肿瘤对伊立替康治疗的反应之间存在统计学上显著的负相关。伊立替康治疗本身并未改变CRC组织中CYP3A5的表达。由于CYP3A5参与伊立替康的降解,在对基于伊立替康的化疗无反应的CRC患者中,肿瘤内CYP3A5表达显著更高可能表明CYP3A5在肿瘤耐药中起因果作用。