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克服癌症中表皮生长因子受体靶向治疗耐药性的探索。

The quest to overcome resistance to EGFR-targeted therapies in cancer.

机构信息

1] Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA. [2] Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

Nat Med. 2013 Nov;19(11):1389-400. doi: 10.1038/nm.3388. Epub 2013 Nov 7.


DOI:10.1038/nm.3388
PMID:24202392
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4049336/
Abstract

All patients with metastatic lung, colorectal, pancreatic or head and neck cancers who initially benefit from epidermal growth factor receptor (EGFR)-targeted therapies eventually develop resistance. An increasing understanding of the number and complexity of resistance mechanisms highlights the Herculean challenge of killing tumors that are resistant to EGFR inhibitors. Our growing knowledge of resistance pathways provides an opportunity to develop new mechanism-based inhibitors and combination therapies to prevent or overcome therapeutic resistance in tumors. We present a comprehensive review of resistance pathways to EGFR-targeted therapies in lung, colorectal and head and neck cancers and discuss therapeutic strategies that are designed to circumvent resistance.

摘要

所有最初从表皮生长因子受体 (EGFR) 靶向治疗中获益的转移性肺、结直肠、胰腺或头颈部癌症患者最终都会产生耐药性。对耐药机制数量和复杂性的认识不断加深,凸显了杀死对 EGFR 抑制剂耐药的肿瘤的巨大挑战。我们对耐药途径的认识不断提高,为开发新的基于机制的抑制剂和联合疗法以预防或克服肿瘤的治疗耐药性提供了机会。我们全面回顾了肺、结直肠和头颈部癌症中针对 EGFR 靶向治疗的耐药途径,并讨论了旨在规避耐药性的治疗策略。

相似文献

[1]
The quest to overcome resistance to EGFR-targeted therapies in cancer.

Nat Med. 2013-11-7

[2]
Molecular-Targeted Therapies for Epidermal Growth Factor Receptor and Its Resistance Mechanisms.

Int J Mol Sci. 2017-11-15

[3]
Strategies to Overcome Bypass Mechanisms Mediating Clinical Resistance to EGFR Tyrosine Kinase Inhibition in Lung Cancer.

Mol Cancer Ther. 2017-2

[4]
Mechanisms of resistance to EGFR targeted therapies.

Cancer Biol Ther. 2013-1-28

[5]
Therapeutic targeting of the epidermal growth factor receptor in human cancer.

Crit Rev Oncog. 2012

[6]
Therapeutic strategies utilized in the setting of acquired resistance to EGFR tyrosine kinase inhibitors.

Clin Cancer Res. 2014-12-1

[7]
A Third Shot at EGFR: New Opportunities in Cancer Therapy.

Trends Pharmacol Sci. 2019-11-6

[8]
EGFR-TKIs resistance via EGFR-independent signaling pathways.

Mol Cancer. 2018-2-19

[9]
Therapeutic targeting of epidermal growth factor receptor in human cancer: successes and limitations.

Chin J Cancer. 2011-1

[10]
New strategies in head and neck cancer: understanding resistance to epidermal growth factor receptor inhibitors.

Clin Cancer Res. 2010-4-20

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本文引用的文献

[1]
A novel serum protein signature associated with resistance to epidermal growth factor receptor tyrosine kinase inhibitors in head and neck squamous cell carcinoma.

Eur J Cancer. 2013-4-10

[2]
Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA.

Nature. 2013-4-7

[3]
Primary resistance to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in patients with non-small-cell lung cancer harboring TKI-sensitive EGFR mutations: an exploratory study.

Ann Oncol. 2013-4-4

[4]
A mechanism of resistance to gefitinib mediated by cellular reprogramming and the acquisition of an FGF2-FGFR1 autocrine growth loop.

Oncogenesis. 2013-3-25

[5]
Acquired resistance to EGFR inhibitors is associated with a manifestation of stem cell-like properties in cancer cells.

Cancer Res. 2013-3-29

[6]
Activation of the FGF2-FGFR1 autocrine pathway: a novel mechanism of acquired resistance to gefitinib in NSCLC.

Mol Cancer Res. 2013-3-27

[7]
PUMA and BIM are required for oncogene inactivation-induced apoptosis.

Sci Signal. 2013-3-26

[8]
Analysis of tumor specimens at the time of acquired resistance to EGFR-TKI therapy in 155 patients with EGFR-mutant lung cancers.

Clin Cancer Res. 2013-3-7

[9]
Second-generation epidermal growth factor receptor tyrosine kinase inhibitors in lung cancers.

J Natl Compr Canc Netw. 2013-2-1

[10]
Epidermal growth factor receptor tyrosine kinase inhibitor-resistant disease.

J Clin Oncol. 2013-2-11

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