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本文引用的文献

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Tumor TP53 expression status, body mass index and prognosis in colorectal cancer.结直肠癌中肿瘤 TP53 表达状态、体重指数与预后的关系。
Int J Cancer. 2012 Sep 1;131(5):1169-78. doi: 10.1002/ijc.26495. Epub 2011 Nov 19.
2
Identification of small-molecule inhibitors of the colorectal cancer oncogene Krüppel-like factor 5 expression by ultrahigh-throughput screening.通过超高速筛选鉴定结直肠癌癌基因 Krüppel 样因子 5 表达的小分子抑制剂。
Mol Cancer Ther. 2011 Nov;10(11):2043-51. doi: 10.1158/1535-7163.MCT-11-0550. Epub 2011 Sep 1.
3
S100A4-induced cell motility and metastasis is restricted by the Wnt/β-catenin pathway inhibitor calcimycin in colon cancer cells.S100A4 诱导的细胞迁移和转移被结肠癌细胞中的 Wnt/β-连环蛋白通路抑制剂钙敏感受体抑制。
Mol Biol Cell. 2011 Sep;22(18):3344-54. doi: 10.1091/mbc.E10-09-0739. Epub 2011 Jul 27.
4
Mutations in the p53 Tumor Suppressor Gene: Important Milestones at the Various Steps of Tumorigenesis.p53肿瘤抑制基因的突变:肿瘤发生各个阶段的重要里程碑。
Genes Cancer. 2011 Apr;2(4):466-74. doi: 10.1177/1947601911408889.
5
RAS Interaction with PI3K: More Than Just Another Effector Pathway.RAS与PI3K的相互作用:不仅仅是另一条效应器途径。
Genes Cancer. 2011 Mar;2(3):261-74. doi: 10.1177/1947601911408079.
6
Recent advances in p53 research and cancer treatment.p53研究与癌症治疗的最新进展。
J Biomed Biotechnol. 2011;2011:978312. doi: 10.1155/2011/978312. Epub 2011 Jun 16.
7
Targeting PI3K signaling as a therapeutic approach for colorectal cancer.针对结直肠癌的 PI3K 信号靶向治疗。
Gastroenterology. 2011 Jul;141(1):50-61. doi: 10.1053/j.gastro.2011.05.010.
8
Dynamics of adherens junctions in epithelial establishment, maintenance, and remodeling.上皮细胞建立、维持和重塑过程中黏着连接的动态变化。
J Cell Biol. 2011 Mar 21;192(6):907-17. doi: 10.1083/jcb.201009141.
9
EGFR Signaling in Colorectal Carcinoma.结直肠癌中的表皮生长因子受体信号传导
Patholog Res Int. 2011 Feb 14;2011:932932. doi: 10.4061/2011/932932.
10
An RNAi-based chemical genetic screen identifies three small-molecule inhibitors of the Wnt/wingless signaling pathway.基于 RNAi 的化学遗传学筛选鉴定出三种 Wnt/wingless 信号通路的小分子抑制剂。
Proc Natl Acad Sci U S A. 2011 Apr 12;108(15):5954-63. doi: 10.1073/pnas.1017496108. Epub 2011 Mar 10.

高通量筛选策略在结直肠癌治疗化合物的靶向鉴定中的应用。

High-throughput screening strategies for targeted identification of therapeutic compounds in colorectal cancer.

机构信息

Department of Medicine, Stony Brook University School of Medicine, HSC-T17 Room 090, Stony Brook, NY 11794, USA.

出版信息

Future Oncol. 2012 Mar;8(3):259-72. doi: 10.2217/fon.12.19.

DOI:10.2217/fon.12.19
PMID:22409463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3425953/
Abstract

Recent advancements in understanding the role of both genetics and molecular pathways in the formation and progression of colorectal cancer have allowed the identification of factors that may be targeted for drug discovery. During the past decade, various approaches have been developed to target specific steps or components of these pathways in order to prevent the development and progression of colorectal cancer and to treat this disease. The innovation and optimization of high-throughput screening methods, as well as the recent emphasis from the NIH on translational sciences, have enabled rapid progress in drug discovery in many fields, including colorectal cancer. Here we present a summary of the recent efforts of targeted high-throughput drug discovery directed at pathways affected in colorectal cancer.

摘要

近年来,人们对遗传和分子途径在结直肠癌形成和发展中的作用的认识不断深入,这使得人们能够识别出可能成为药物研发靶点的因素。在过去的十年中,已经开发出各种方法来针对这些途径的特定步骤或成分进行靶向治疗,以预防结直肠癌的发生和发展,并治疗这种疾病。高通量筛选方法的创新和优化,以及 NIH 最近对转化科学的重视,使得包括结直肠癌在内的许多领域的药物发现取得了快速进展。在这里,我们总结了针对结直肠癌相关途径的靶向高通量药物发现的最新努力。