Telomere length regulation through epidermal growth factor receptor signaling in cancer.

Q2 Biochemistry, Genetics and Molecular Biology Genes and Cancer Pub Date : 2017-05-01 DOI:10.18632/genesandcancer.140
Titto Augustine, Radhashree Maitra, Sanjay Goel
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引用次数: 14

Abstract

Length of the telomere (TL), a structure at the tip of chromosome that protects and ensures stability, is determined by multi-protein complexes such as telosome/shelterin and telomerase. Earlier studies from our laboratory show that longer TL has potential to be positive predictive biomarker of clinical outcome to anti-epidermal growth factor receptor (EGFR) monoclonal antibody therapy in patients with KRAS WT metastatic colorectal cancer. Although there is extensive literature suggesting the role of shelterin and telomerase, not much literature exists that describes the role of EGFR and KRAS pathway in regulating TL. This detailed review focuses on an insight into various components, including proteins, enzymes and transcription factors, interlinking between EGFR pathways and telomerase that regulate TL.

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肿瘤中表皮生长因子受体信号对端粒长度的调控。
端粒(TL)是位于染色体顶端的一种保护和确保稳定性的结构,其长度由端粒/庇护蛋白和端粒酶等多蛋白复合物决定。我们实验室的早期研究表明,较长的TL有可能成为KRAS WT转移性结直肠癌患者抗表皮生长因子受体(EGFR)单克隆抗体治疗临床结果的阳性预测生物标志物。尽管有大量文献表明庇护蛋白和端粒酶的作用,但描述EGFR和KRAS通路在调节TL中的作用的文献并不多。本文将详细介绍EGFR通路和端粒酶之间调节TL的各种成分,包括蛋白质、酶和转录因子。
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来源期刊
Genes and Cancer
Genes and Cancer Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.90
自引率
0.00%
发文量
6
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