Division of Medical Biochemistry, Biocenter, Innsbruck Medical University, Innsbruck, Austria.
Molecular Oncology Group, Department of Obstetrics and Gynecology, Comprehensive Cancer Center - Gynecologic Cancer Unit, Medical University of Vienna, Vienna, Austria.
Gynecol Oncol. 2018 May;149(2):371-380. doi: 10.1016/j.ygyno.2018.02.020. Epub 2018 Mar 9.
Circulating tumor cells (CTCs) may represent a chronic stimulus for the immune system. In the present study we investigated the potential association of CTCs, the immune activation marker neopterin, and the ratio of kynurenine to tryptophan (Kyn/Trp) as a measure for tryptophan breakdown.
Neopterin, tryptophan and kynurenine levels were measured in plasma samples from patients with benign gynecological diseases (n=65) and with primary advanced epithelial ovarian cancer (EOC) at diagnosis (n=216) and six months after adjuvant platinum-based chemotherapy (n=45) by an enzyme-linked immunosorbent assay and high performance liquid chromatography. The presence of CTCs had been assessed in a previous study by qPCR-based analysis of CTC-related transcripts in the blood. The respective plasma levels in EOC and benign samples were compared using a two-tailed Chi or Fisher's exact test. The associations of the analytes and Kyn/Trp with clinicopathological parameters, platinum-sensitivity, and the presence of CTC-related transcripts were assessed using a two-sided t-test. Associations with patient outcome were evaluated using Cox regression analysis.
In EOC, elevated Kyn/Trp and neopterin levels were associated with advanced disease, peritoneal carcinomatosis, ascites, sub-optimal debulking, poor response to therapy and worse outcome. Likewise, neopterin and Kyn/Trp were elevated in CTC-positive patients, both at diagnosis and at follow-up in platinum-sensitive disease.
We observed concomitant alterations of CTCs and immune system related biomarkers suggesting that immune responses along with increase of neopterin and Kyn/Trp concentrations are not necessarily only located at the site of the tumor, but may also go on in the circulation.
循环肿瘤细胞(CTC)可能代表免疫系统的慢性刺激。本研究我们调查了 CTC、免疫激活标志物新蝶呤和色氨酸分解产物犬尿氨酸与色氨酸的比值(Kyn/Trp)之间的潜在关联。
采用酶联免疫吸附试验和高效液相色谱法检测 65 例良性妇科疾病患者和 216 例初诊晚期上皮性卵巢癌(EOC)患者及 45 例接受辅助铂类化疗后 6 个月时的血浆样本中的新蝶呤、色氨酸和犬尿氨酸水平。先前的研究通过 qPCR 分析血液中的 CTC 相关转录本评估了 CTC 的存在。采用双侧 Chi 或 Fisher 确切检验比较 EOC 和良性样本中的相应血浆水平。采用双侧 t 检验评估分析物和 Kyn/Trp 与临床病理参数、铂敏感性和 CTC 相关转录本的相关性。采用 Cox 回归分析评估与患者预后的相关性。
在 EOC 中,升高的 Kyn/Trp 和新蝶呤水平与晚期疾病、腹膜种植、腹水、减瘤不充分、治疗反应不佳和预后不良相关。同样,在 CTC 阳性患者中,无论是在诊断时还是在铂类敏感疾病的随访中,新蝶呤和 Kyn/Trp 均升高。
我们观察到 CTC 和免疫系统相关生物标志物的同时改变,这表明免疫反应以及新蝶呤和 Kyn/Trp 浓度的增加不仅位于肿瘤部位,而且可能在循环中继续进行。