| Literature DB >> 33707749 |
Yuanwang Pan1, Han Han1, Kristen E Labbe1, Hua Zhang2, Kwok-Kin Wong3.
Abstract
Lung squamous cell carcinoma (LUSC) represents a major subtype of non-small cell lung cancer with limited treatment options. Previous studies have elucidated the complex genetic landscape of LUSC and revealed multiple altered genes and pathways. However, in stark contrast to lung adenocarcinoma, few targetable driver mutations have been established so far and targeted therapies for LUSC remain unsuccessful. Immunotherapy has revolutionized LUSC treatment and is currently approved as the new standard of care. To gain a better understanding of the LUSC biology, improved modeling systems are urgently needed. Preclinical models, particularly those mimicking human disease with an intact tumor immune microenvironment, are an invaluable tool to study cancer development and evaluate new therapeutic targets. Here, we discuss recent advances in LUSC preclinical models, with a focus on genetically engineered mouse models (GEMMs) and organoids, in the context of evolving precision medicine and immunotherapy.Entities:
Mesh:
Year: 2021 PMID: 33707749 DOI: 10.1038/s41388-021-01723-7
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867