摘要:锯齿状通路在结直肠癌早期检测中的靶向成像研究

Thomas D. Wang
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摘要

背景与意义:结直肠癌(CRC)是癌症相关死亡的主要原因,全球约有140万新发病例,每年约有69万例死亡。锯齿状通路是近端结肠结直肠癌的主要原因。无柄锯齿状腺瘤(SSA)具有扁平和细微的特征,难以用常规白光结肠镜检查出来。目的:我们的目的是确定一种肽显像剂,可以特异性结合SSA来改善近端结肠恶性病变的可视化。方法:对BRAF V600E点突变细胞采用减影生物筛选噬菌体展示技术。我们进行了首次人体临床研究,在n = 38名人类受试者的近端结肠中局部施用这种fitc标记的肽,并使用对荧光敏感的宽视场内窥镜进行体内成像。结果:鉴定出肽序列KCCFPAQ,测得表观解离常数kd = 72 nM,表观结合时间常数kd = 0.174 min-1 (5.76 min)。在活体荧光图像上,我们测量到SSA的靶背景比正常结肠粘膜高2.43倍,并且能够以89%的灵敏度和92%的特异性区分SSA。我们发现区分SSA与传统腺瘤的敏感性为84%,特异性为91%。在动物或患者研究中,均未发现该肽具有毒性。在离体图像上,我们发现SSA的平均荧光强度明显大于增生性息肉。结论:我们已经确定了一种可安全用于临床的荧光标记肽,并且可以通过宽视场成像特异性地检测近端结肠中的SSAs。这种有针对性的成像方法可能有助于在常规结肠镜检查中早期发现恶性前锯齿状病变。引用格式:Thomas D. Wang。锯齿状通路在结直肠癌早期检测中的靶向成像研究。[摘要]。摘自:AACR特别会议论文集:改进癌症风险预测以预防和早期发现;2016年11月16日至19日;费城(PA): AACR;Cancer epidemiology Biomarkers pre2017;26(5增刊):摘要nr - IA10。
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Abstract IA10: Targeted imaging of the serrated pathway for early detection of colorectal cancer
Background and Significance: Colorectal cancer (CRC) is a leading cause of cancer-related mortality with ~1.4 million new cases diagnosed globally and ~690,000 annual deaths. The serrated pathway is a primary cause of CRC in the proximal colon. Sessile serrated adenomas (SSA) have flat and subtle features that are difficult to detect with conventional white light colonoscopy. Aims: We aim to identify a peptide imaging agent that binds specifically to SSA to improve visualization of pre-malignant lesions in the proximal colon. Methods: We used phage display technology with subtractive biopanning against cells with a V600E point mutation in BRAF. We performed a first-in-humans clinical study by topically administering this FITC-labeled peptide in the proximal colon of n = 38 human subjects, and performed in vivo imaging using a wide-field endoscope that is sensitive to fluorescence. Results: We identified the peptide sequence KCCFPAQ, and measured an apparent dissociation constant of kd = 72 nM and an apparent association time constant of kd = 0.174 min-1 (5.76 min). On in vivo fluorescence images, we measured a 2.43-fold greater target-to-background ratio for SSA than for normal colonic mucosa, and could distinguish SSA with 89% sensitivity and 92% specificity. We found 84% sensitivity and 91% specificity for discriminating SSA from traditional adenomas. No toxicity was attributed to the peptide in either animal or patient studies. On ex vivo images, we found the mean fluorescence intensity for SSA to be significantly greater than that for hyperplastic polyps. Conclusions: We have identified a fluorescently-labeled peptide that is safe for clinical use, and is specific for detecting SSAs in the proximal colon with wide-field imaging. This targeted imaging methodology may be useful for early detection of pre-malignant serrated lesions on routine colonoscopy. Citation Format: Thomas D. Wang. Targeted imaging of the serrated pathway for early detection of colorectal cancer. [abstract]. In: Proceedings of the AACR Special Conference: Improving Cancer Risk Prediction for Prevention and Early Detection; Nov 16-19, 2016; Orlando, FL. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2017;26(5 Suppl):Abstract nr IA10.
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