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结直肠癌的个性化治疗:新进展与潜在治疗策略

Personalized treatment for colorectal cancer: novel developments and putative therapeutic strategies.

作者信息

Akkad Jamil, Bochum Sylvia, Martens Uwe M

机构信息

Cancer Center Heilbronn-Franken, SLK Kliniken Heilbronn GmbH, Heilbronn, Germany.

出版信息

Langenbecks Arch Surg. 2015 Feb;400(2):129-43. doi: 10.1007/s00423-015-1276-0. Epub 2015 Feb 10.

DOI:10.1007/s00423-015-1276-0
PMID:25701352
Abstract

BACKGROUND

Colorectal cancer (CRC) is the third most common cancer diagnosed worldwide and continues to be a major healthcare concern. Molecular heterogeneity of CRC is believed to be one of the main factors responsible for the considerable variability in treatment response. With the recent development of powerful genomic technologies, novel insights in tumor biology of CRC have now been provided, facilitating the recognition of new molecular subtypes with prognostic and predictive implications.

PURPOSE

The purpose of this review article is to summarize current knowledge about genomic, epigenomic, and proteomic characteristics of CRC, as well as their implications for biomarker identification and individualized targeted therapy.

CONCLUSION

Supplementing the findings from several previous studies, the Cancer Genome Atlas (TCGA) project recently finalized the systematic characterization of CRC resulting in the first tumor dataset with complete molecular measurements at DNA, RNA, and protein levels. The challenge now is to translate these findings into a robust and reproducible CRC classification system linking molecular features of the tumor to precision medicine.

摘要

背景

结直肠癌(CRC)是全球第三大常见诊断癌症,仍然是主要的医疗保健问题。CRC的分子异质性被认为是治疗反应存在显著差异的主要因素之一。随着强大基因组技术的最新发展,现在已经对CRC的肿瘤生物学有了新的见解,有助于识别具有预后和预测意义的新分子亚型。

目的

这篇综述文章的目的是总结关于CRC的基因组、表观基因组和蛋白质组特征的当前知识,以及它们对生物标志物识别和个体化靶向治疗的意义。

结论

癌症基因组图谱(TCGA)项目补充了之前几项研究的结果,最近完成了对CRC的系统表征,产生了第一个在DNA、RNA和蛋白质水平进行完整分子测量的肿瘤数据集。现在的挑战是将这些发现转化为一个强大且可重复的CRC分类系统,将肿瘤的分子特征与精准医学联系起来。

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Hsa_circRNA_002144 promotes growth and metastasis of colorectal cancer through regulating miR-615-5p/LARP1/mTOR pathway.hsa_circRNA_002144 通过调控 miR-615-5p/LARP1/mTOR 通路促进结直肠癌细胞的生长和转移。

本文引用的文献

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Antiangiogenesis strategies revisited: from starving tumors to alleviating hypoxia.抗血管生成策略再探讨:从饿死肿瘤到缓解缺氧
Cancer Cell. 2014 Nov 10;26(5):605-22. doi: 10.1016/j.ccell.2014.10.006.
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Human cancer immunotherapy with antibodies to the PD-1 and PD-L1 pathway.使用针对PD-1和PD-L1通路的抗体进行人类癌症免疫治疗。
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Aspirin for colorectal cancer with PIK3CA mutations: the rising of the oldest targeted therapy?用于治疗携带PIK3CA突变的结直肠癌的阿司匹林:最古老的靶向治疗正在兴起?
Carcinogenesis. 2021 Apr 30;42(4):601-610. doi: 10.1093/carcin/bgaa140.
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In-Depth Characterization of Mass Spectrometry-Based Proteomic Profiles Revealed Novel Signature Proteins Associated with Liver Metastatic Colorectal Cancers.基于质谱的蛋白质组学特征深度分析揭示了与结直肠癌肝转移相关的新型特征性蛋白。
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Strategy to targeting the immune resistance and novel therapy in colorectal cancer.靶向结直肠癌免疫抵抗的策略和新疗法。
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Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target.LARP1的过表达预示着结直肠癌的预后不良,有望成为一个潜在的治疗靶点。
Tumour Biol. 2016 Nov;37(11):14585-14594. doi: 10.1007/s13277-016-5332-3. Epub 2016 Sep 10.
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Advances in targeted and immunobased therapies for colorectal cancer in the genomic era.基因组时代结直肠癌靶向治疗和免疫治疗的进展
Onco Targets Ther. 2016 Mar 31;9:1899-920. doi: 10.2147/OTT.S95101. eCollection 2016.
8
Nuclear Factor Kappa B, Matrix Metalloproteinase-1, p53, and Ki-67 Expressions in the Primary Tumors and the Lymph Node Metastases of Colorectal Cancer Cases.结直肠癌原发灶和淋巴结转移灶中核因子-κB、基质金属蛋白酶-1、p53 和 Ki-67 的表达。
Gastroenterol Res Pract. 2015;2015:945392. doi: 10.1155/2015/945392. Epub 2015 Apr 6.
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Mol Med Rep. 2015 Aug;12(2):1838-44. doi: 10.3892/mmr.2015.3594. Epub 2015 Apr 3.
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Clin Cancer Res. 2014 Dec 15;20(24):6429-38. doi: 10.1158/1078-0432.CCR-14-0774. Epub 2014 Jun 10.