肠道灌洗液中的 5α 还原酶基因水平会随着结直肠癌的进展而降低。

Tadashi Fujii, Yoshihito Nakagawa, Kohei Funasaka, Yoshiki Hirooka, Takumi Tochio
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引用次数: 0

摘要

简介结肠直肠癌(CRC)是癌症死亡的主要原因,与肠道微生物群和胆汁酸代谢密切相关。二级胆汁酸(如脱氧胆酸和石胆酸)会破坏重要的细胞功能,从而增加患 CRC 的风险。相比之下,异全胆酸(isoalloLCA)具有潜在的健康益处,这凸显了胆汁酸在 CRC 中的复杂作用。我们之前开发了一套特异引物,用于扩增参与异全胆酸生物合成的 5α 还原酶基因(5ar)的同源物,从而能够估算肠道中 5ar 的丰度(5ar 水平)。我们假设肠道中的5ar水平与CRC有关。本研究旨在调查肠道中的5ar水平,并在腺瘤-癌序列的不同阶段对其进行比较,为监测CRC风险的新策略提供见解。从144例结肠镜检查收集的肠道灌洗液(ILF)中提取DNA。我们采用下一代测序技术(NGS)检测了 5ar 同源物的序列,使用特定引物组检测了 7 个选定 ILF 的 DNA,其中 4 个来自癌症患者,3 个来自非肿瘤粘膜患者。此外,我们还使用定量 PCR(qPCR)技术测定了所有 144 份 DNA 样本中的 5ar 水平。我们进行了 144 次结肠镜检查,并根据腺瘤-癌症顺序对患者进行了分类:52例为非肿瘤性粘膜,69例为腺瘤,23例为癌。对 292,042 个 NGS 导出的 5ar 序列进行分析后发现了七个最常见的扩增片段序列变异,每个变异长度为 254 碱基对。这些变体与均匀乳杆菌(Bacteroides uniformis)、秃头乳杆菌(Phocaeicola vulgatus)和多雷乳杆菌(Phocaeicola dorei)的 5ar 序列密切匹配或完全相同。此外,qPCR 分析表明,与非肿瘤粘膜组相比,癌变组的 5ar 水平明显较低(P = 0.0004)。腺瘤组中也观察到类似的趋势,但无统计学意义(P = 0.0763),这表明随着 CRC 的发展,5ar 水平会降低。这些研究结果表明,基于 PCR 技术监测肠道样本中 5ar 水平的变化可为评估 CRC 风险的增加提供一种无创、快速且经济有效的方法。
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Levels of 5α-reductase gene in intestinal lavage fluid decrease with progression of colorectal cancer.

Introduction. Colorectal cancer (CRC) is a leading cause of cancer deaths, closely linked to the intestinal microbiota and bile acid metabolism. Secondary bile acids, like deoxycholic and lithocholic acid, are associated with increased CRC risk due to their disruption of vital cellular functions. In contrast, isoallolithocholic acid (isoalloLCA) shows potential health benefits, highlighting the complex role of bile acids in CRC. A specific primer set was previously developed to amplify homologs of the 5α-reductase gene (5ar), which are involved in the biosynthesis of isoalloLCA, thereby enabling the estimation of abundance of 5ar (5ar levels) in the intestine.Hypothesis/Gap Statement. We hypothesized that 5ar levels in the intestine are associated with CRC.Aim. This study aimed to investigate intestinal 5ar levels and compare them across different stages of the adenoma-carcinoma sequence, providing insights into novel strategies for monitoring CRC risk.Methodology. DNA was extracted from intestinal lavage fluids (ILF) collected during 144 colonoscopies. Next-generation sequencing (NGS) was employed to examine the sequence of 5ar homologues, using a specific primer set on DNA from seven selected ILFs - four from carcinoma patients and three from individuals with non-neoplastic mucosa. Additionally, we used quantitative PCR (qPCR) to measure 5ar levels in all 144 DNA samples.Results. We conducted 144 colonoscopies and categorized patients according to the adenoma-cancer sequence: 52 with non-neoplastic mucosa, 69 with adenomas and 23 with carcinoma. Analysis of 292,042 NGS-derived 5ar sequences revealed the seven most prevalent amplicon sequence variants, each 254 base pairs in length. These closely matched or were identical to 5ar sequences in Bacteroides uniformis, Phocaeicola vulgatus and Phocaeicola dorei. Furthermore, qPCR analysis demonstrated significantly lower 5ar levels in the carcinoma group compared to those in the non-neoplastic mucosa group (P = 0.0004). A similar, though not statistically significant, trend was observed in the adenoma group (P = 0.0763), suggesting that 5ar levels decrease as CRC progresses.Conclusion. These findings indicate that PCR-based monitoring of 5ar levels in intestinal samples over time could provide a non-invasive, rapid and cost-effective method for assessing an increased risk of CRC.

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