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通过条件重编程细胞培养建立内镜超声引导下活检的胰腺癌细胞系。

Establishment of pancreatic cancer cell lines with endoscopic ultrasound-guided biopsy via conditionally reprogrammed cell culture.

机构信息

Division of Gastroenterology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.

Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Cancer Med. 2019 Jul;8(7):3339-3348. doi: 10.1002/cam4.2210. Epub 2019 May 1.

DOI:10.1002/cam4.2210
PMID:31044541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6601705/
Abstract

Recent studies have identified the mutational landscape of pancreatic cancer and suggested tumor-specific subtypes. However, the major hurdle against personalized treatment is the difficulty to obtain sufficient cancer tissues from most inoperable cases. We investigated whether patient-derived conditionally reprogrammed cells (CRCs) can be constructed using a small piece of tumor tissue using endoscopic ultrasound (EUS)-guided fine needle biopsy (FNB). Thirty patients with pancreatic solid mass (mean size, 34.6 mm) were enrolled prospectively. Among 22 patients who were diagnosed with pancreatic ductal adenocarcinoma, we established patient-derived pancreatic cancer cell lines from eight patients (36.4%). Immunofluorescence colony staining for CRCs showed that the cytoplasm of cancer cells was clearly stained with anti-cytokeratin 19 monoclonal antibody. In the soft agar colony formation assay, CRCs formed colonies compared with the negative control by day 15. In vivo, implanted CRCs showed tumor engraftment and hematoxylin and eosin staining showed pancreatic cancer ductal structure. All established CRCs showed a KRAS mutation. In conclusion, we established patient-derived pancreatic cancer cell lines with a small tumor tissue obtained by EUS-FNB. With in vitro drug sensitivity and genomic studies, established patient-derived cell lines can be used in identification of new targets for diagnosis and treatment of pancreatic cancer.

摘要

最近的研究已经确定了胰腺癌的突变特征,并提出了肿瘤特异性亚型。然而,个性化治疗的主要障碍是难以从大多数无法手术的病例中获得足够的癌症组织。我们通过内镜超声(EUS)引导的细针活检(FNB),研究了能否使用小块肿瘤组织构建患者来源的条件重编程细胞(CRC)。前瞻性纳入 30 名胰腺实体瘤患者(平均大小 34.6mm)。在 22 名被诊断为胰腺导管腺癌的患者中,我们从 8 名患者(36.4%)中建立了患者来源的胰腺癌细胞系。CRC 的免疫荧光集落染色显示,抗细胞角蛋白 19 单克隆抗体可清晰染色癌细胞的细胞质。在软琼脂集落形成试验中,CRC 在第 15 天形成集落,而阴性对照则没有。在体内,植入的 CRC 显示出肿瘤移植,苏木精和伊红染色显示出胰腺导管结构。所有建立的 CRC 均显示 KRAS 突变。总之,我们通过 EUS-FNB 从小块肿瘤组织中建立了患者来源的胰腺癌细胞系。通过体外药物敏感性和基因组研究,可以使用建立的患者来源细胞系来鉴定用于诊断和治疗胰腺癌的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/55f7c77ff012/CAM4-8-3339-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/5c83c601bc9c/CAM4-8-3339-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/abece5332acd/CAM4-8-3339-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/d9394ad9ef10/CAM4-8-3339-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/88db95c57e3f/CAM4-8-3339-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/55f7c77ff012/CAM4-8-3339-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/5c83c601bc9c/CAM4-8-3339-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/abece5332acd/CAM4-8-3339-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/d9394ad9ef10/CAM4-8-3339-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/88db95c57e3f/CAM4-8-3339-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cc/6601705/55f7c77ff012/CAM4-8-3339-g005.jpg

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