Li Tao, Huang Jin-Bo, Lu Jun-Guo, Li Rong, Wang Yan, Shi Xiang-Rong, Shi Min-Xin, Zhang Xiao-Dong
Department of Medical Oncology, Nantong Tumor Hospital, Nantong, China.
Department of Respiratory Medicine, Affiliated Hospital of Nantong University, Nantong, China.
J Thorac Dis. 2020 Dec;12(12):7313-7319. doi: 10.21037/jtd-20-3185.
High levels of thymidylate synthase (TS) and dihydrofolate reductase (DHFR) expression in tumour tissues are an indicator of ineffective responses to pemetrexed-based chemotherapy in various tumours, including non-small cell lung cancer (NSCLC). However, tumour tissues are highly heterogeneous, so a single biopsy may not reflect genetic alterations during disease progression. This study investigated the potential use of plasma TS and DHFR mRNA levels as biomarkers for predicting sensitivity to pemetrexed-based chemotherapy.
Plasma samples were obtained from 245 patients with advanced NSCLC and 30 healthy donors. Total RNA was extracted from the plasma samples, and TS and DHFR mRNA levels were determined via real-time PCR. TS and DHFR mRNA levels between cancer patients and healthy controls were compared. The association between plasma TS and DHFR mRNA levels and tumour response to pemetrexed/cisplatin chemotherapy was analysed.
The plasma TS and DHFR mRNA levels decreased in patients with advanced NSCLC compared with healthy controls. Moreover, plasma TS and DHFR mRNA levels negatively correlated with tumour response to pemetrexed/cisplatin chemotherapy in patients with advanced NSCLC. Overall survival time was prolonged in patients with low TS mRNA expression compared with those with high TS mRNA expression, although the difference was not statistically significant.
Low expression levels of plasma TS and DHFR mRNA confer increased tumour sensitivity to pemetrexed/cisplatin chemotherapy in patients with advanced NSCLC. The results suggested that plasma TS and DHFR mRNA levels are promising biomarkers for choosing patients who are likely to respond and benefit the most from pemetrexed-based chemotherapy.
肿瘤组织中胸苷酸合成酶(TS)和二氢叶酸还原酶(DHFR)的高表达是包括非小细胞肺癌(NSCLC)在内的各种肿瘤对培美曲塞为基础的化疗反应不佳的一个指标。然而,肿瘤组织具有高度异质性,因此单次活检可能无法反映疾病进展过程中的基因改变。本研究调查了血浆TS和DHFR mRNA水平作为预测培美曲塞为基础的化疗敏感性生物标志物的潜在用途。
从245例晚期NSCLC患者和30名健康供体中获取血浆样本。从血浆样本中提取总RNA,并通过实时PCR测定TS和DHFR mRNA水平。比较癌症患者和健康对照者之间的TS和DHFR mRNA水平。分析血浆TS和DHFR mRNA水平与培美曲塞/顺铂化疗的肿瘤反应之间的关联。
与健康对照相比,晚期NSCLC患者的血浆TS和DHFR mRNA水平降低。此外,晚期NSCLC患者的血浆TS和DHFR mRNA水平与培美曲塞/顺铂化疗的肿瘤反应呈负相关。TS mRNA低表达患者的总生存时间比高表达患者延长,尽管差异无统计学意义。
晚期NSCLC患者血浆TS和DHFR mRNA低表达使肿瘤对培美曲塞/顺铂化疗的敏感性增加。结果表明,血浆TS和DHFR mRNA水平是选择可能从培美曲塞为基础的化疗中最有可能产生反应并获益的患者的有前景的生物标志物。