克拉斯
神经母细胞瘤RAS病毒癌基因同源物
赫拉
结直肠癌
医学
癌基因
肿瘤科
内科学
病毒癌基因
肺癌
癌症研究
SMARCA4型
肉瘤
基因
癌症
病理
基因表达
遗传学
生物
染色质重塑
细胞周期
作者
Umberto Malapelle,Francesco Passiglia,Chiara Cremolini,Maria Lucia Reale,Francesco Pepe,Pasquale Pisapia,Antonio Avallone,Diego Cortinovis,Alfonso De Stefano,Matteo Fassan,Gabriella Fontanini,Domenico Galetta,Calogero Lauricella,Angela Listì,Fotios Loupakis,Fabio Pagni,Filippo Pietrantonio,Sara Pilotto,Luisella Righi,Andrea Sartore‐Bianchi
标识
DOI:10.1016/j.ejca.2021.01.015
摘要
Rat sarcoma (RAS) oncogenes have intensively been investigated during the last decades. Taking into account all human tumours, Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) gene is the most frequently mutated (about 22%) among the three isoforms, followed by Neuroblastoma RAS Viral Oncogene Homolog (NRAS) (8%) and Harvey Rat Sarcoma Viral Oncogene Homolog (HRAS) (3%). In the last years, careful attention has been paid on KRAS and NRAS gene mutations in non–small-cell lung cancer (NSCLC) and colorectal cancer (CRC) patients because of their prognostic and predictive roles. In particular, a large body of literature data has been generated investigating clinical outcomes of targeted treatments in NSCLC and CRC KRAS- and NRAS-mutated patients. The latest evidences are here reviewed, providing also an overview of the real-world RAS mutation testing practice across different Italian laboratories. On this basis, we propose a knowledge-based system, www.rasatlas.com, to support the healthcare personnel in the management of patients featuring RAS gene mutations in the landscape of precision oncology.
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