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Lung Adenocarcinoma Tumor Origin: A Guide for Personalized Medicine
被引:94
|作者:
Seguin, Laetitia
[1
]
Durandy, Manon
[1
]
Feral, Chloe C.
[1
]
机构:
[1] Univ Cote dAzur, FHU Oncoage, IRCAN, CNRS,INSERM, F-06107 Nice, France
来源:
关键词:
LUAD;
cell of origin;
lung progenitor;
oncogenic driver;
immune infiltration;
CANCER STEM-CELLS;
GENOMIC ALTERATIONS;
MUTANT KRAS;
OF-ORIGIN;
IDENTIFICATION;
REGENERATION;
DRIVEN;
BMI1;
RAS;
RESISTANCE;
D O I:
10.3390/cancers14071759
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Simple Summary Lung cancer is the leading cause of cancer-related death worldwide, with an average 5-year survival rate of approximately 15%. Among the multiple histological type of lung cancer, adenocarcinoma is the most common. Adenocarcinoma is characterized by a high degree of heterogeneity at many levels, including histological, cellular, and molecular. Understanding the cell of origin of adenocarcinoma, and the molecular changes during tumor progression, will allow better therapeutic strategies. Lung adenocarcinoma, the major form of lung cancer, is the deadliest cancer worldwide, due to its late diagnosis and its high heterogeneity. Indeed, lung adenocarcinoma exhibits pronounced inter- and intra-tumor heterogeneity cofounding precision medicine. Tumor heterogeneity is a clinical challenge driving tumor progression and drug resistance. Several key pieces of evidence demonstrated that lung adenocarcinoma results from the transformation of progenitor cells that accumulate genetic abnormalities. Thus, a better understanding of the cell of origin of lung adenocarcinoma represents an opportunity to unveil new therapeutic alternatives and stratify patient tumors. While the lung is remarkably quiescent during homeostasis, it presents an extensive ability to respond to injury and regenerate lost or damaged cells. As the lung is constantly exposed to potential insult, its regenerative potential is assured by several stem and progenitor cells. These can be induced to proliferate in response to injury as well as differentiate into multiple cell types. A better understanding of how genetic alterations and perturbed microenvironments impact progenitor-mediated tumorigenesis and treatment response is of the utmost importance to develop new therapeutic opportunities.
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页数:15
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