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建立、功能和遗传表征三种新型的患者来源的直肠癌细胞系。

Establishment, functional and genetic characterization of three novel patient-derived rectal cancer cell lines.

机构信息

Department of General Surgery, University Medical Center, Rostock 18055, Germany.

Section of Molecular Oncology and Immunotherapy, University Medical Center, Rostock 18055, Germany.

出版信息

World J Gastroenterol. 2018 Nov 21;24(43):4880-4892. doi: 10.3748/wjg.v24.i43.4880.

Abstract

AIM

To establish patient-individual tumor models of rectal cancer for analyses of novel biomarkers, individual response prediction and individual therapy regimens.

METHODS

Establishment of cell lines was conducted by direct culturing and xenografting with subsequent culturing. Cell lines were in-depth characterized concerning morphological features, invasive and migratory behavior, phenotype, molecular profile including mutational analysis, protein expression, and confirmation of origin by DNA fingerprint. Assessment of chemosensitivity towards an extensive range of current chemotherapeutic drugs and of radiosensitivity was performed including analysis of a combined radio- and chemotherapeutic treatment. In addition, glucose metabolism was assessed with F-fluorodeoxyglucose (FDG) and proliferation with F-fluorothymidine.

RESULTS

We describe the establishment of ultra-low passage rectal cancer cell lines of three patients suffering from rectal cancer. Two cell lines (HROC126, HROC284Met) were established directly from tumor specimens while HROC239 T0 M1 was established subsequent to xenografting of the tumor. Molecular analysis classified all three cell lines as CIMP-0/ non-MSI-H (sporadic standard) type. Mutational analysis revealed following mutational profiles: HROC126: , , , , ; HROC239 T0 M1: , , , , and HROC284Met: , , , , . All cell lines could be characterized as epithelial (EpCAM) tumor cells with equivalent morphologic features and comparable growth kinetics. The cell lines displayed a heterogeneous response toward chemotherapy, radiotherapy and their combined application. HROC126 showed a highly radio-resistant phenotype and HROC284Met was more susceptible to a combined radiochemotherapy than HROC126 and HROC239 T0 M1. Analysis of F-FDG uptake displayed a markedly reduced FDG uptake of all three cell lines after combined radiochemotherapy.

CONCLUSION

These newly established and in-depth characterized ultra-low passage rectal cancer cell lines provide a useful instrument for analysis of biological characteristics of rectal cancer.

摘要

目的

建立直肠癌个体化肿瘤模型,用于分析新型生物标志物、预测个体反应和制定个体化治疗方案。

方法

通过直接培养和异种移植,然后进行培养,建立细胞系。对细胞系进行深入的表型特征、侵袭和迁移行为、表型、分子谱(包括突变分析、蛋白表达)分析,以及通过 DNA 指纹确认来源。评估对广泛的当前化疗药物和放射敏感性的化疗敏感性,包括分析联合放射和化学治疗。此外,还使用 F-氟脱氧葡萄糖(FDG)评估葡萄糖代谢,使用 F-氟胸苷评估增殖。

结果

我们描述了建立三位直肠癌患者的超低传代直肠癌细胞系。两个细胞系(HROC126、HROC284Met)直接从肿瘤标本中建立,而 HROC239 T0 M1 是从肿瘤异种移植后建立的。分子分析将所有三个细胞系分类为 CIMP-0/非 MSI-H(散发性标准)型。突变分析显示以下突变谱:HROC126: 、 、 、 、 ;HROC239 T0 M1: 、 、 、 、 ,和 HROC284Met: 、 、 、 、 。所有细胞系均能被鉴定为上皮(EpCAM)肿瘤细胞,具有相同的形态特征和相似的生长动力学。细胞系对化疗、放疗及其联合应用表现出异质性反应。HROC126 表现出高度放射抵抗表型,而 HROC284Met 比 HROC126 和 HROC239 T0 M1 更易受到联合放化疗的影响。分析 F-FDG 摄取显示,所有三种细胞系在联合放化疗后 FDG 摄取明显减少。

结论

这些新建立的和深入表征的超低传代直肠癌细胞系为分析直肠癌的生物学特征提供了有用的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa0/6250916/fe899f45edce/WJG-24-4880-g001.jpg

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