Current Approaches in NSCLC Targeting K-RAS and EGFR

被引:58
|
作者
Aran, Veronica [1 ]
Omerovic, Jasminka [2 ]
机构
[1] Natl Inst Traumatol & Orthoped, Res Div, Av Brasil 500, BR-20940070 Rio De Janeiro, Brazil
[2] Univ Split, Sch Med, Soltanska 2, Split 21000, Croatia
关键词
lung cancer; NSCLC; K-RAS; EGFR; lung cancer therapy; EPIDERMAL-GROWTH-FACTOR; CELL LUNG-CANCER; TYROSINE KINASE INHIBITOR; SYNTHETIC LETHAL INTERACTION; FACTOR RECEPTOR EGFR; ACQUIRED-RESISTANCE; T790M MUTATION; 1ST-LINE TREATMENT; DRUG-RESISTANCE; INCREASED SENSITIVITY;
D O I
10.3390/ijms20225701
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The research and treatment of non-small cell lung cancer (NSCLC) have achieved some important advances in recent years. Nonetheless, the overall survival rates for NSCLC remain low, indicating the importance to effectively develop new therapies and improve current approaches. The understanding of the function of different biomarkers involved in NSCLC progression, survival and response to therapy are important for the development of early detection tools and treatment options. Epidermal growth factor receptor (EGFR) and Kirsten rat sarcoma viral oncogene homolog (K-RAS) are two of the main significant biomarkers for the management of NSCLC. Mutations in these genes were associated with development and response to therapies. For example, the use of small molecule tyrosine kinase (TK) inhibitors and immunotherapy has led to benefits in some, but not all patients with altered EGFR. In contrast, there is still no effective approved drug to act upon patients harbouring K-RAS mutations. In addition, K-RAS mutations have been associated with lack of activity of TK inhibitors. However, promising approaches aimed to inhibit mutant K-RAS are currently under study. Therefore, this review will discuss these approaches and also EGFR therapies, and hopefully, it will draw attention to the need of continued research in the field in order to improve the outcomes in NSCLC patients.
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页数:24
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