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促纤维增生性小圆细胞瘤(DSRCT)异种移植瘤及组织培养系:建立与初步表征

Desmoplastic small round cell tumor (DSRCT) xenografts and tissue culture lines: Establishment and initial characterization.

作者信息

Markides Constantine S A, Coil Douglas R, Luong Linh H, Mendoza John, Kozielski Tony, Vardeman Dana, Giovanella Beppino C

机构信息

Christus Stehlin Foundation for Cancer Research, Houston, TX 77025, USA.

出版信息

Oncol Lett. 2013 May;5(5):1453-1456. doi: 10.3892/ol.2013.1265. Epub 2013 Mar 19.

Abstract

Desmoplastic small round cell tumor (DSRCT) is an extremely rare and aggressive neoplasm, which mainly affects young males and generally presents as a widely disseminated tumor within the peritoneal cavity. Due to the rarity of the tumor, its younger and overall healthier patient population (compared with other tumor types) and the fact that it lacks definitive histological and immunohistological features, the diagnosis of DSRCT may be frequently delayed or the tumor may be entirely misdiagnosed as a different type of abdominal sarcoma. The present study aimed to rectify the lack of models that exist for this rare neoplasm, through the development of several DSRCT tissue cultures and xenograft lines. Samples were received from surgeries and biopsies from patients worldwide and were immediately processed for xenograft development in nude mice. Tumor tissues were minced and fragments were injected into the dorsal flanks of nude mice. Of the 14 samples received, nine were established into xenograft lines and five into tissue culture lines. Xenografts displayed the microscopic histology of their parent tumors and demonstrated two different growth rates among the established xenograft lines. Overall, the establishment of these xenograft and tissue culture lines provides researchers with tools to evaluate DSRCT responses to chemotherapy and to investigate DSRCT-specific signaling pathways or mechanisms.

摘要

促纤维组织增生性小圆细胞肿瘤(DSRCT)是一种极其罕见且侵袭性强的肿瘤,主要影响年轻男性,通常表现为广泛播散于腹腔内的肿瘤。由于该肿瘤罕见,其患者群体相对年轻且整体健康状况较好(与其他肿瘤类型相比),以及缺乏明确的组织学和免疫组织学特征,DSRCT的诊断可能经常延迟,或者肿瘤可能被完全误诊为其他类型的腹部肉瘤。本研究旨在通过开发几种DSRCT组织培养物和异种移植系来弥补这种罕见肿瘤现有模型的不足。样本来自世界各地患者的手术和活检组织,并立即用于裸鼠异种移植的开发。将肿瘤组织切碎,把碎片注射到裸鼠的背部侧翼。在收到的14个样本中,9个建立了异种移植系,5个建立了组织培养系。异种移植显示出其亲本肿瘤的微观组织学特征,并且在已建立的异种移植系中表现出两种不同的生长速率。总体而言,这些异种移植系和组织培养系的建立为研究人员提供了工具,用于评估DSRCT对化疗的反应以及研究DSRCT特异性信号通路或机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c91f/3678573/f68e2b0dda5d/OL-05-05-1453-g00.jpg

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