Lack of CD8 + T cell effector differentiation during priming mediates checkpoint blockade resistance in non–small cell lung cancer

2021 ◽  
Vol 6 (64) ◽  
Author(s):  
Brendan L. Horton ◽  
Duncan M. Morgan ◽  
Noor Momin ◽  
Maria Zagorulya ◽  
Elen Torres-Mejia ◽  
...  
Lung Cancer ◽  
2003 ◽  
Vol 41 ◽  
pp. S46-S47
Author(s):  
Luis E. Raez ◽  
Peter A. Cassileth ◽  
James Schlesselman ◽  
Swaminathan Padmanabhan ◽  
Eva Fisher ◽  
...  

2010 ◽  
Vol 59 (10) ◽  
pp. 1467-1479 ◽  
Author(s):  
Lee M. Krug ◽  
Tao Dao ◽  
Andrew B. Brown ◽  
Peter Maslak ◽  
William Travis ◽  
...  

2021 ◽  
Vol 429 ◽  
pp. 118843
Author(s):  
Marc Hardwick ◽  
Luke Nolan ◽  
James Nicoll ◽  
Sanjay Jogai ◽  
Edurne Arriola ◽  
...  

BMC Medicine ◽  
2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Zhihui Zhang ◽  
Chaoqi Zhang ◽  
Yuejun Luo ◽  
Peng Wu ◽  
Guochao Zhang ◽  
...  

Abstract Background Small cell lung cancer (SCLC) is lethal and possesses limited therapeutic options. Platinum-based chemotherapy—with or without immune checkpoint inhibitors (anti-PDs)—is the current first-line therapy for SCLCs; however, its associated outcomes are heterogeneous. N6-methyladenosine (m6A) is a novel and decisive factor in tumour progression, chemotherapy resistance, and immunotherapy response. However, m6A modification in SCLC remains poorly understood. Methods We systematically explored the molecular features and clinical significance of m6A regulators in SCLC. We then constructed an m6A regulator-based prognostic signature (m6A score) based on our examination of 256 cases with limited-stage SCLC (LS-SCLC) from three different cohorts—including an independent cohort that contained 150 cases with qPCR data. We additionally evaluated the relationships between the m6A score and adjuvant chemotherapy (ACT) benefits and the patients’ responses to anti-PD-1 treatment. Immunohistochemical (IHC) staining and the HALO digital pathological platform were used to calculate CD8+ T cell density. Results We observed abnormal somatic mutations and expressions of m6A regulators. Using the LASSO Cox model, a five-regulator-based (G3BP1, METTL5, ALKBH5, IGF2BP3, and RBM15B) m6A score was generated from the significant regulators to classify patients into high- and low-score groups. In the training cohort, patients with high scores had shorter overall survival (HR, 5.19; 2.75–9.77; P < 0.001). The prognostic accuracy of the m6A score was well validated in two independent cohorts (HR 4.6, P = 0.006 and HR 3.07, P < 0.001). Time-dependent ROC and C-index analyses found the m6A score to possess superior predictive power than other clinicopathological parameters. A multicentre multivariate analysis revealed the m6A score to be an independent prognostic indicator. Additionally, patients with low scores received a greater survival benefit from ACT, exhibited more CD8+ T cell infiltration, and were more responsive to cancer immunotherapy. Conclusions Our results, for the first time, affirm the significance of m6A regulators in LS-SCLC. Our multicentre analysis found that the m6A score was a reliable prognostic tool for guiding chemotherapy and immunotherapy selections for patients with SCLC.


2018 ◽  
Vol 24 (7) ◽  
pp. 994-1004 ◽  
Author(s):  
Daniela S. Thommen ◽  
Viktor H. Koelzer ◽  
Petra Herzig ◽  
Andreas Roller ◽  
Marcel Trefny ◽  
...  

Author(s):  
Sehui Kim ◽  
Ji-Young Jang ◽  
Jaemoon Koh ◽  
Dohee Kwon ◽  
Young A. Kim ◽  
...  

Abstract Background We investigated the role of PD-L1 in the metabolic reprogramming of non-small cell lung cancer (NSCLC). Methods Changes in glycolysis-related molecules and glycolytic activity were evaluated in PD-L1low and PD-L1high NSCLC cells after transfection or knockdown of PD-L1, respectively. Jurkat T-cell activation was assessed after co-culture with NSCLC cells. The association between PD-L1 and immune response-related molecules or glycolysis were analyzed in patients with NSCLC and The Cancer Genome Atlas (TCGA). Results Transfecting PD-L1 in PD-L1low cells enhanced hexokinase-2 (HK2) expression, lactate production, and extracellular acidification rates, but minimally altered GLUT1 and PKM2 expression and oxygen consumption rates. By contrast, knocking-down PD-L1 in PD-L1high cells decreased HK2 expression and glycolysis by suppressing PI3K/Akt and Erk pathways. Interferon-γ (IFNγ) secretion and activation marker expression was decreased in stimulated Jurkat T-cells when co-cultured with HK2-overexpressing vector-transfected tumor cells rather than empty vector-transfected tumor cells. Immunohistochemistry revealed that PD-L1 expression was positively correlated with HK2 expression in NSCLC (p < 0.001). In TCGA, HK2 exhibited a positive linear association with CD274 (PD-L1) expression (p < 0.001) but an inverse correlation with the expression of CD4, CD8A, and T-cell effector function-related genes in the CD274high rather than CD274low group. Consistently, there were fewer CD8+ T-cells in PD-L1positive/HK2high tumors compared to PD-L1positive/HK2low tumors in squamous cell carcinoma. Conclusions PD-L1 enhances glycolysis in NSCLC by upregulating HK2, which might dampen anti-tumor immunity. PD-L1 may contribute to NSCLC oncogenesis by inducing metabolic reprogramming and immune checkpoint.


2012 ◽  
Vol 131 (5) ◽  
pp. E649-E658 ◽  
Author(s):  
Yoshihiro Ohue ◽  
Shingo Eikawa ◽  
Nami Okazaki ◽  
Yu Mizote ◽  
Midori Isobe ◽  
...  

Lung Cancer ◽  
2019 ◽  
Vol 136 ◽  
pp. 30-36 ◽  
Author(s):  
Eun-Ah Choe ◽  
Yoon Jin Cha ◽  
Jae-Hwan Kim ◽  
Kyoung Ho Pyo ◽  
Min Hee Hong ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document