Cargando…

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

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 s...

Descripción completa

Detalles Bibliográficos
Autores principales: Pons-Tostivint, Elvire, Lugat, Alexandre, Fontenau, Jean-François, Denis, Marc Guillaume, Bennouna, Jaafar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618117/
https://www.ncbi.nlm.nih.gov/pubmed/34831355
http://dx.doi.org/10.3390/cells10113129
_version_ 1784604670563450880
author Pons-Tostivint, Elvire
Lugat, Alexandre
Fontenau, Jean-François
Denis, Marc Guillaume
Bennouna, Jaafar
author_facet Pons-Tostivint, Elvire
Lugat, Alexandre
Fontenau, Jean-François
Denis, Marc Guillaume
Bennouna, Jaafar
author_sort Pons-Tostivint, Elvire
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8618117
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86181172021-11-27 STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact Pons-Tostivint, Elvire Lugat, Alexandre Fontenau, Jean-François Denis, Marc Guillaume Bennouna, Jaafar Cells Review 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. MDPI 2021-11-11 /pmc/articles/PMC8618117/ /pubmed/34831355 http://dx.doi.org/10.3390/cells10113129 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pons-Tostivint, Elvire
Lugat, Alexandre
Fontenau, Jean-François
Denis, Marc Guillaume
Bennouna, Jaafar
STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact
title STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact
title_full STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact
title_fullStr STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact
title_full_unstemmed STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact
title_short STK11/LKB1 Modulation of the Immune Response in Lung Cancer: From Biology to Therapeutic Impact
title_sort stk11/lkb1 modulation of the immune response in lung cancer: from biology to therapeutic impact
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618117/
https://www.ncbi.nlm.nih.gov/pubmed/34831355
http://dx.doi.org/10.3390/cells10113129
work_keys_str_mv AT ponstostivintelvire stk11lkb1modulationoftheimmuneresponseinlungcancerfrombiologytotherapeuticimpact
AT lugatalexandre stk11lkb1modulationoftheimmuneresponseinlungcancerfrombiologytotherapeuticimpact
AT fontenaujeanfrancois stk11lkb1modulationoftheimmuneresponseinlungcancerfrombiologytotherapeuticimpact
AT denismarcguillaume stk11lkb1modulationoftheimmuneresponseinlungcancerfrombiologytotherapeuticimpact
AT bennounajaafar stk11lkb1modulationoftheimmuneresponseinlungcancerfrombiologytotherapeuticimpact