Department of Colorectal Surgery, Tianjin Union Medical Center, Nankai University Tianjin Institute of Coloproctology, Tianjin, China.
Department of Traditional Chinese Medicine, Shanghai Pudong New Area People's Hospital, Shanghai, Tanjin, China.
Pharmazie. 2021 Dec 5;76(12):606-610. doi: 10.1691/ph.2021.1780.
The mutation status of the gene involved in early colorectal carcinogenesis and micro-invasive liquid biopsy allows detection of mutated circulating tumor DNA (ctDNA). Early detection of precancerous lesions and CRC is vital in proper treatment and hence associated to patient survival. The frequency of APC, CTNNB1, KRAS, and BRAF mutations in circulating free DNA (cfDNA) were analyzed to evaluate the performance of the mutated ctDNA in detecting polyp and adenoma using highly sensitive QClamp XNA based PCR. A total of 71 patients with low-risk adenoma or polyps were screened and there was no significant difference in the distribution of mutations gender, age, long-term medication, smoking history, alcohol drinking, and fecal occult blood. The positive predictive value (PPV) of the four genes' panel to detect low-risk adenoma and polyps was 39.44% (n = 28/71). Specifically, of all the 71 cases studied, there were 20 cases (28.2%) with APC mutations, 7 cases (9.9%) with CTNNB1 mutations, 4 cases (5.6%) with KRAS mutations, and 2 cases (2.8%) with BRAF mutations. Most mutations occurred at APC876. The four genes' panel detected by XNA-based PCR technique might be suited to efficiently and micro-invasively detect genetic alterations in cfDNA of patients with precancerous colorectal lesions.
涉及结直肠癌早期发生和微侵袭性液体活检的基因突变状态可检测到突变的循环肿瘤 DNA(ctDNA)。癌前病变和 CRC 的早期检测对于正确的治疗至关重要,因此与患者的生存相关。分析循环游离 DNA(cfDNA)中 APC、CTNNB1、KRAS 和 BRAF 基因突变的频率,以评估基于高度敏感的 QClamp XNA 的 PCR 检测息肉和腺瘤中突变 ctDNA 的性能。对 71 例低危腺瘤或息肉患者进行了筛查,基因突变在性别、年龄、长期用药、吸烟史、饮酒史和粪便潜血方面的分布无显著差异。该 panel 对低危腺瘤和息肉的阳性预测值(PPV)为 39.44%(n=28/71)。具体而言,在研究的 71 例病例中,APC 突变 20 例(28.2%),CTNNB1 突变 7 例(9.9%),KRAS 突变 4 例(5.6%),BRAF 突变 2 例(2.8%)。大多数突变发生在 APC876。基于 XNA 的 PCR 技术检测的 panel 可能适合于有效地微创检测癌前结直肠病变患者 cfDNA 中的遗传改变。