STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact

被引:58
作者
Pons-Tostivint, Elvire [1 ,2 ]
Lugat, Alexandre [2 ]
Fontenau, Jean-Francois [2 ]
Denis, Marc Guillaume [3 ]
Bennouna, Jaafar [2 ,4 ]
机构
[1] Nantes Univ Hosp, Med Oncol Dept, F-44000 Nantes, France
[2] Univ Nantes, INSERM, UMR 1232, Ctr Res Cancerol & Immunol Nantes Angers CRCINA, F-44000 Nantes, France
[3] Nantes Univ Hosp, Dept Biochem, F-44000 Nantes, France
[4] Hop Foch, Med Oncol Dept, F-75073 Suresnes, France
关键词
STK11/LKB1; non-small cell lung cancer; immunotherapy; biomarker; KRAS; PEUTZ-JEGHERS-SYNDROME; COOCCURRING GENOMIC ALTERATIONS; PROGNOSTIC IMPACT; PROTEIN-KINASE; LKB1; AMPK; KRAS; METABOLISM; LKB1/STK11; MUTATIONS;
D O I
10.3390/cells10113129
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The STK11/LKB1 gene codes for liver kinase B1 (STK11/LKB1), a highly conserved serine/threonine kinase involved in many energy-related cellular processes. The canonical tumor-suppressive role for STK11/LKB1 involves the activation of AMPK-related kinases, a master regulator of cell survival during stress conditions. In pre-clinical models, inactivation of STK11/LKB1 leads to the progression of lung cancer with the acquisition of metastatic properties. Moreover, preclinical and clinical data have shown that inactivation of STK11/LKB1 is associated with an inert tumor immune microenvironment, with a reduced density of infiltrating cytotoxic CD8(+) T lymphocytes, a lower expression of PD-(L)1, and a neutrophil-enriched tumor microenvironment. In this review, we first describe the biological function of STK11/LKB1 and the role of its inactivation in cancer cells. We report descriptive epidemiology, co-occurring genomic alterations, and prognostic impact for lung cancer patients. Finally, we discuss recent data based on pre-clinical models and lung cancer cohorts analyzing the results of STK11/LKB1 alterations on the immune system and response or resistance to immune checkpoint inhibitors.
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页数:17
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