• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胰腺癌细胞系的表型和基因型。

Phenotype and genotype of pancreatic cancer cell lines.

机构信息

Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.

出版信息

Pancreas. 2010 May;39(4):425-35. doi: 10.1097/MPA.0b013e3181c15963.

DOI:10.1097/MPA.0b013e3181c15963
PMID:20418756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2860631/
Abstract

The dismal prognosis of pancreatic adenocarcinoma is due in part to a lack of molecular information regarding disease development. Established cell lines remain a useful tool for investigating these molecular events. Here we present a review of available information on commonly used pancreatic adenocarcinoma cell lines as a resource to help investigators select the cell lines most appropriate for their particular research needs. Information on clinical history; in vitro and in vivo growth characteristics; phenotypic characteristics, such as adhesion, invasion, migration, and tumorigenesis; and genotypic status of commonly altered genes (KRAS, p53, p16, and SMAD4) was evaluated. Identification of both consensus and discrepant information in the literature suggests careful evaluation before selection of cell lines and attention be given to cell line authentication.

摘要

胰腺腺癌预后不佳的部分原因是缺乏有关疾病发展的分子信息。已建立的细胞系仍然是研究这些分子事件的有用工具。在这里,我们回顾了常用胰腺腺癌细胞系的现有信息,以帮助研究人员选择最适合其特定研究需求的细胞系。评估了临床病史;体外和体内生长特性;表型特征,如粘附、侵袭、迁移和致瘤性;以及常见改变基因(KRAS、p53、p16 和 SMAD4)的基因型状态。文献中一致和不一致信息的识别表明,在选择细胞系之前需要仔细评估,并应注意细胞系的鉴定。

相似文献

1
Phenotype and genotype of pancreatic cancer cell lines.胰腺癌细胞系的表型和基因型。
Pancreas. 2010 May;39(4):425-35. doi: 10.1097/MPA.0b013e3181c15963.
2
Genomic sequencing of key genes in mouse pancreatic cancer cells.对小鼠胰腺癌细胞中关键基因进行基因组测序。
Curr Mol Med. 2012 Mar;12(3):331-41. doi: 10.2174/156652412799218868.
3
[Genetic aspects of pancreatic cancer].[胰腺癌的遗传学方面]
Eksp Klin Gastroenterol. 2014(10):70-6.
4
Clinical Effect of Driver Mutations of , and in Pancreatic Cancer: A Meta-Analysis.胰腺癌中 、 和 驱动基因突变的临床效应:一项荟萃分析。
Genet Test Mol Biomarkers. 2020 Dec;24(12):777-788. doi: 10.1089/gtmb.2020.0078.
5
Clinical significance of the genetic landscape of pancreatic cancer and implications for identification of potential long-term survivors.胰腺癌的遗传特征及其对潜在长期生存者识别的临床意义。
Clin Cancer Res. 2012 Nov 15;18(22):6339-47. doi: 10.1158/1078-0432.CCR-12-1215. Epub 2012 Sep 18.
6
[Will molecular diagnostics become established in pancreatic pathology?].分子诊断会在胰腺病理学中确立地位吗?
Pathologe. 2013 Nov;34 Suppl 2:214-20. doi: 10.1007/s00292-013-1865-z.
7
Genetics and Biology of Pancreatic Ductal Adenocarcinoma.胰腺导管腺癌的遗传学与生物学
Hematol Oncol Clin North Am. 2015 Aug;29(4):595-608. doi: 10.1016/j.hoc.2015.04.003. Epub 2015 Jun 10.
8
The Roles of Frequently Mutated Genes of Pancreatic Cancer in Regulation of Tumor Microenvironment.胰腺癌常见突变基因在肿瘤微环境调节中的作用
Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820920969. doi: 10.1177/1533033820920969.
9
Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.源自细胞系和原发性肿瘤且具有不同转移活性的胰腺腺癌原位移植模型。
Pancreas. 2004 Oct;29(3):193-203. doi: 10.1097/00006676-200410000-00004.
10
Five primary human pancreatic adenocarcinoma cell lines established by the outgrowth method.五种通过体外培养方法建立的人胰腺导管腺癌细胞系。
J Surg Res. 2012 Jan;172(1):29-39. doi: 10.1016/j.jss.2011.04.021. Epub 2011 May 7.

引用本文的文献

1
Bridging the gap: the role of 3D cell cultures in mimicking tumor microenvironment for enhanced drug testing accuracy.弥合差距:3D细胞培养在模拟肿瘤微环境以提高药物测试准确性方面的作用。
Front Bioeng Biotechnol. 2025 Aug 12;13:1498141. doi: 10.3389/fbioe.2025.1498141. eCollection 2025.
2
ATF4-mediated expression of NOXA is critical for Necroptosis driven by Glucose Deprivation.ATF4介导的NOXA表达对于葡萄糖剥夺驱动的坏死性凋亡至关重要。
Front Cell Death. 2025;3. doi: 10.3389/fceld.2024.1507960. Epub 2025 Jan 20.
3
Pro-Apoptotic Effects of Unsymmetrical Bisacridines in 3D Pancreatic Multicellular Tumor Spheroids.

本文引用的文献

1
HPAC, a new human glucocorticoid-sensitive pancreatic ductal adenocarcinoma cell line.HPAC,一种新的人糖皮质激素敏感型胰腺导管腺癌细胞系。
In Vitro Cell Dev Biol Anim. 1994 Mar;30A(3):151-61. doi: 10.1007/BF02631438.
2
Epithelial to mesenchymal transition contributes to drug resistance in pancreatic cancer.上皮-间质转化促进胰腺癌的耐药性。
Cancer Res. 2009 Jul 15;69(14):5820-8. doi: 10.1158/0008-5472.CAN-08-2819. Epub 2009 Jul 7.
3
Core signaling pathways in human pancreatic cancers revealed by global genomic analyses.
不对称双吖啶在三维胰腺多细胞肿瘤球体中的促凋亡作用
Int J Mol Sci. 2025 Aug 5;26(15):7557. doi: 10.3390/ijms26157557.
4
Immune infiltration and stromal heterogeneity in pancreatic cancer: A prognostic model guiding immunotherapy response.胰腺癌中的免疫浸润和基质异质性:指导免疫治疗反应的预后模型
Oncol Lett. 2025 Jul 29;30(4):465. doi: 10.3892/ol.2025.15211. eCollection 2025 Oct.
5
The use of pancreatic ductal adenocarcinoma 2D and 3D models to evaluate NDV infection, replication and induced cell death.使用胰腺导管腺癌二维和三维模型评估新城疫病毒感染、复制及诱导的细胞死亡。
Sci Rep. 2025 Jul 1;15(1):22178. doi: 10.1038/s41598-025-06023-8.
6
Pan-Cancer Analysis Identifies a Ras-Related GTPase as a Potential Modulator of Cancer.泛癌分析确定一种Ras相关GTP酶为癌症的潜在调节因子。
Int J Mol Sci. 2025 May 6;26(9):4419. doi: 10.3390/ijms26094419.
7
The kinase domain of TRPM7 interacts with PAK1 and regulates pancreatic cancer cell epithelial-to-mesenchymal transition.瞬时受体电位阳离子通道亚家族M成员7(TRPM7)的激酶结构域与p21激活激酶1(PAK1)相互作用,并调节胰腺癌细胞的上皮-间质转化。
Cell Death Dis. 2025 Apr 24;16(1):335. doi: 10.1038/s41419-025-07665-2.
8
Target-Specific Locked Nucleic Acid Gapmer Decreases Growth and Metastases of Pancreatic Cancer.靶向特异性锁核酸 Gapmer 可降低胰腺癌的生长和转移。
Mol Cancer Ther. 2025 Aug 1;24(8):1277-1288. doi: 10.1158/1535-7163.MCT-24-1059.
9
Jorunnamycin A induces apoptosis in pancreatic ductal adenocarcinoma cells, spheroids, and patient-derived organoids by modulating KRAS-mediated survival pathways.乔鲁纳霉素A通过调节KRAS介导的生存途径,诱导胰腺导管腺癌细胞、球体和患者来源的类器官发生凋亡。
Sci Rep. 2025 Apr 3;15(1):11376. doi: 10.1038/s41598-025-95766-5.
10
Quantitative characterization of the 3D self-organization of PDAC tumor spheroids reveals cell type and matrix dependence through advanced microscopy analysis.通过先进的显微镜分析对胰腺导管腺癌(PDAC)肿瘤球体的三维自组织进行定量表征,揭示了细胞类型和基质依赖性。
APL Bioeng. 2025 Mar 27;9(1):016116. doi: 10.1063/5.0242490. eCollection 2025 Mar.
通过全基因组分析揭示的人类胰腺癌核心信号通路。
Science. 2008 Sep 26;321(5897):1801-6. doi: 10.1126/science.1164368. Epub 2008 Sep 4.
4
Natural history of pancreatic cancer recurrence following "curative" resection in athymic mice.无胸腺小鼠“根治性”切除术后胰腺癌复发的自然病史。
J Surg Res. 2008 Sep;149(1):57-61. doi: 10.1016/j.jss.2007.08.024. Epub 2007 Sep 18.
5
Gene expression profile of metastatic human pancreatic cancer cells depends on the organ microenvironment.转移性人胰腺癌细胞的基因表达谱取决于器官微环境。
Cancer Res. 2007 Jan 1;67(1):139-48. doi: 10.1158/0008-5472.CAN-06-2563.
6
Multi-scale modeling of a wound-healing cell migration assay.伤口愈合细胞迁移试验的多尺度建模
J Theor Biol. 2007 Apr 7;245(3):576-94. doi: 10.1016/j.jtbi.2006.10.024. Epub 2006 Oct 28.
7
Selective blockade of vascular endothelial growth factor receptor 2 with an antibody against tumor-derived vascular endothelial growth factor controls the growth of human pancreatic adenocarcinoma xenografts.用抗肿瘤源性血管内皮生长因子的抗体选择性阻断血管内皮生长因子受体2可控制人胰腺腺癌异种移植瘤的生长。
Ann Surg Oncol. 2006 Aug;13(8):1145-55. doi: 10.1245/ASO.2006.05.049. Epub 2006 Jun 21.
8
Pancreatic cancer cells invasiveness is mainly affected by interleukin-1beta not by transforming growth factor-beta1.胰腺癌细胞的侵袭性主要受白细胞介素-1β影响,而非转化生长因子-β1。
Int J Biol Markers. 2005 Oct-Dec;20(4):235-41. doi: 10.1177/172460080502000406.
9
Cystic fibrosis transmembrane regulator gene carrier status is a risk factor for young onset pancreatic adenocarcinoma.囊性纤维化跨膜传导调节因子基因携带者状态是青年期胰腺癌的一个危险因素。
Gut. 2005 Nov;54(11):1661-2. doi: 10.1136/gut.2005.074534.
10
Activation of focal adhesion kinase enhances the adhesion and invasion of pancreatic cancer cells via extracellular signal-regulated kinase-1/2 signaling pathway activation.粘着斑激酶的激活通过细胞外信号调节激酶-1/2信号通路的激活增强胰腺癌细胞的粘附和侵袭。
Mol Cancer. 2005 Oct 6;4:37. doi: 10.1186/1476-4598-4-37.