
Cell, Journal Year: 2019, Volume and Issue: 177(7), P. 1842 - 1857.e21
Published: May 30, 2019
Language: Английский
Cell, Journal Year: 2019, Volume and Issue: 177(7), P. 1842 - 1857.e21
Published: May 30, 2019
Language: Английский
Nature reviews. Cancer, Journal Year: 2018, Volume and Issue: 19(1), P. 9 - 31
Published: Dec. 10, 2018
Language: Английский
Citations
908Cell, Journal Year: 2019, Volume and Issue: 176(5), P. 998 - 1013.e16
Published: Jan. 31, 2019
Language: Английский
Citations
756Nature Medicine, Journal Year: 2021, Volume and Issue: 27(8), P. 1345 - 1356
Published: Aug. 1, 2021
Language: Английский
Citations
707Signal Transduction and Targeted Therapy, Journal Year: 2019, Volume and Issue: 4(1)
Published: Dec. 17, 2019
Abstract Lung cancer is one of the most common in world. In 2018, there were over 2 million new cases lung and 1.7 deaths attributed to cancer. Targeted therapy has emerged as an important mean disease management for patients with non-small-cell (NSCLC). Herein, we review analyze recent literature, discuss targeting pathways ongoing clinical trials Chemotherapy no longer best available treatment all patients. Therapeutic decisions should be guided by understanding molecular features patient’s tumor tissues. The future gains will likely emerge from finding optimal ways combining targeted therapy, immunotherapy, chemotherapy.
Language: Английский
Citations
602Cell, Journal Year: 2020, Volume and Issue: 182(1), P. 200 - 225.e35
Published: July 1, 2020
To explore the biology of lung adenocarcinoma (LUAD) and identify new therapeutic opportunities, we performed comprehensive proteogenomic characterization 110 tumors 101 matched normal adjacent tissues (NATs) incorporating genomics, epigenomics, deep-scale proteomics, phosphoproteomics, acetylproteomics. Multi-omics clustering revealed four subgroups defined by key driver mutations, country, gender. Proteomic phosphoproteomic data illuminated downstream copy number aberrations, somatic fusions identified vulnerabilities associated with events involving KRAS, EGFR, ALK. Immune subtyping a complex landscape, reinforced association STK11 immune-cold behavior, underscored potential immunosuppressive role neutrophil degranulation. Smoking-associated LUADs showed correlation other environmental exposure signatures field effect in NATs. Matched NATs allowed identification differentially expressed proteins diagnostic utility. This proteogenomics dataset represents unique public resource for researchers clinicians seeking to better understand treat adenocarcinomas.
Language: Английский
Citations
583Nature Communications, Journal Year: 2021, Volume and Issue: 12(1)
Published: May 5, 2021
Abstract Lung cancer is a highly heterogeneous disease. Cancer cells and within the tumor microenvironment together determine disease progression, as well response to or escape from treatment. To map cell type-specific transcriptome landscape of their in advanced non-small lung (NSCLC), we analyze 42 tissue biopsy samples stage III/IV NSCLC patients by single RNA sequencing present large scale, resolution profiles NSCLCs. In addition types described previous studies early cancer, are able identify rare tumors such follicular dendritic T helper 17 cells. Tumors different display heterogeneity cellular composition, chromosomal structure, developmental trajectory, intercellular signaling network phenotype dominance. Our study also reveals correlation with associated neutrophils, which might help shed light on function NSCLC.
Language: Английский
Citations
565Cell, Journal Year: 2020, Volume and Issue: 182(1), P. 245 - 261.e17
Published: July 1, 2020
Language: Английский
Citations
457Nature Communications, Journal Year: 2021, Volume and Issue: 12(1)
Published: Jan. 12, 2021
Abstract Circular RNAs (circRNA) are a class of covalently closed single-stranded that have been implicated in cancer progression. Here we identify circNDUFB2 to be downregulated non-small cell lung (NSCLC) tissues, and negatively correlate with NSCLC malignant features. Elevated inhibits growth metastasis cells. Mechanistically, functions as scaffold enhance the interaction between TRIM25 IGF2BPs, positive regulator tumor progression metastasis. This TRIM25/circNDUFB2/IGF2BPs ternary complex facilitates ubiquitination degradation this effect enhanced by N 6 -methyladenosine (m A) modification . Moreover, is also recognized RIG-I activate RIG-I-MAVS signaling cascades recruit immune cells into microenvironment (TME). Our data thus provide evidences participates IGF2BPs activation anti-tumor immunity during via modulation both protein degradation, well cellular responses.
Language: Английский
Citations
434Nature Reviews Clinical Oncology, Journal Year: 2020, Volume and Issue: 17(5), P. 279 - 299
Published: Feb. 20, 2020
Language: Английский
Citations
411Critical Reviews in Oncology/Hematology, Journal Year: 2020, Volume and Issue: 157, P. 103194 - 103194
Published: Dec. 11, 2020
Language: Английский
Citations
377