分子生物学改变临床肿瘤学:表皮生长因子受体在结直肠癌中的应用。

IF 6.6 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology Molecular Oncology Pub Date : 2024-10-29 DOI:10.1002/1878-0261.13754
Pietro Paolo Vitiello, Nadia Saoudi González, Alberto Bardelli
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引用次数: 0

摘要

生长因子的发现及其在癌症中的参与是精准肿瘤学的基础。针对结直肠癌(CRC)表皮生长因子受体(EGFR)的药物的临床前和临床开发伴随着巨大的炒作和希望,尽管这些药物的临床试验与内在和获得性耐药性发生冲突,大大限制了它们的治疗价值。然而,随着对表皮生长因子受体(EGFR)信号通路在 CRC 中的生物学作用的深入了解,以及用于实时研究癌症演变的液体活检方法的发展,促进了抗 EGFR 治疗 CRC 的临床完善。这种基于生物学知识和临床发展共同演化的工作流程允许将相关耐药机制的发现与绕过这种耐药的策略开发结合起来。这一范例的更广泛应用将证明是成功的,并为靶向治疗以外的治疗策略提供了一条从实验室到临床的有效捷径。
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When molecular biology transforms clinical oncology: the EGFR journey in colorectal cancer.

The discovery of growth factors and their involvement in cancer represents the foundation of precision oncology. The preclinical and clinical development of agents targeting epidermal growth factor receptor (EGFR) in colorectal cancer (CRC) were accompanied by big hype and hopes, though the clinical testing of such agents clashed with intrinsic and acquired resistance, greatly limiting their therapeutic value. However, a better understanding of the biology of the EGFR signaling pathway in CRC, coupled with the development of liquid biopsy methodologies to study cancer evolution in real time, fostered the clinical refinement of anti-EGFR treatment in CRC. Such a workflow, based on the co-evolution of biology knowledge and clinical development, allowed to couple the discovery of relevant therapy resistance mechanisms to the development of strategies to bypass this resistance. A broader application of this paradigm could prove successful and create an effective shortcut between the bench and the bedside for treatment strategies other than targeted therapy.

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来源期刊
Molecular Oncology
Molecular Oncology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
11.80
自引率
1.50%
发文量
203
审稿时长
10 weeks
期刊介绍: Molecular Oncology highlights new discoveries, approaches, and technical developments, in basic, clinical and discovery-driven translational cancer research. It publishes research articles, reviews (by invitation only), and timely science policy articles. The journal is now fully Open Access with all articles published over the past 10 years freely available.
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