Small-cell lung cancer brain metastasis: From molecular mechanisms to diagnosis and treatment DOI Creative Commons
Yingze Zhu,

Yishuang Cui,

Xuan Zheng

и другие.

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Год журнала: 2022, Номер 1868(12), С. 166557 - 166557

Опубликована: Сен. 24, 2022

Lung cancer is the most malignant human worldwide, also with highest incidence rate. However, small-cell lung (SCLC) accounts for 14 % of all cases. Approximately 10 patients SCLC have brain metastasis at time diagnosis, which leading cause death worldwide. The median overall survival only 4.9 months, and a long-tern cure exists due to limited common therapeutic options. Recent studies enhanced our understanding molecular mechanisms meningeal metastasis, multimodality treatments brought new hopes better disease. This review aimed offer an insight into cellular processes different metastatic stages revealed by established animal models, major diagnostic methods SCLC. Additionally, it provided in-depth information on recent advances in treatments, highlighted several models biomarkers promises improve prognosis

Язык: Английский

Proteogenomic Characterization Reveals Therapeutic Vulnerabilities in Lung Adenocarcinoma DOI Creative Commons
Michael A. Gillette, Shankha Satpathy, Song Cao

и другие.

Cell, Год журнала: 2020, Номер 182(1), С. 200 - 225.e35

Опубликована: Июль 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.

Язык: Английский

Процитировано

577

Targeted Therapies for Lung Cancer Patients With Oncogenic Driver Molecular Alterations DOI
Aaron C. Tan, Daniel S.W. Tan

Journal of Clinical Oncology, Год журнала: 2022, Номер 40(6), С. 611 - 625

Опубликована: Янв. 5, 2022

Lung cancer has traditionally been classified by histology. However, a greater understanding of disease biology and the identification oncogenic driver alterations dramatically altered therapeutic landscape. Consequently, new classification paradigm non-small-cell lung is further characterized molecularly defined subsets actionable with targeted therapies treatment landscape becoming increasingly complex. This review encompasses current standards care for in molecular alterations. Targeted EGFR exon 19 deletion L858R mutations, ALK ROS1 rearrangements are well established. there an expanding list approved including BRAF V600E, 20 insertion, KRAS G12C MET 14 alterations, NTRK RET rearrangements. In addition, numerous other drivers, such as HER2 insertion which emerging efficacy data therapies. The importance diagnostic testing, intracranial novel therapies, optimal sequencing role early-stage disease, future directions precision oncology approaches to understand tumor evolution resistance also discussed.

Язык: Английский

Процитировано

477

The technological landscape and applications of single-cell multi-omics DOI Open Access
Alev Baysoy, Zhiliang Bai, Rahul Satija

и другие.

Nature Reviews Molecular Cell Biology, Год журнала: 2023, Номер 24(10), С. 695 - 713

Опубликована: Июнь 6, 2023

Язык: Английский

Процитировано

438

Lung adenocarcinoma promotion by air pollutants DOI
William Hill, Emilia L. Lim, Clare E. Weeden

и другие.

Nature, Год журнала: 2023, Номер 616(7955), С. 159 - 167

Опубликована: Апрель 5, 2023

Язык: Английский

Процитировано

412

Genetic and non-genetic clonal diversity in cancer evolution DOI
James R. Black, Nicholas McGranahan

Nature reviews. Cancer, Год журнала: 2021, Номер 21(6), С. 379 - 392

Опубликована: Март 16, 2021

Язык: Английский

Процитировано

226

Antitumour immunity regulated by aberrant ERBB family signalling DOI
Shogo Kumagai, Shohei Koyama, Hiroyoshi Nishikawa

и другие.

Nature reviews. Cancer, Год журнала: 2021, Номер 21(3), С. 181 - 197

Опубликована: Янв. 18, 2021

Язык: Английский

Процитировано

204

A high-stringency blueprint of the human proteome DOI Creative Commons
Subash Adhikari, Edouard C. Nice, Eric W. Deutsch

и другие.

Nature Communications, Год журнала: 2020, Номер 11(1)

Опубликована: Окт. 16, 2020

Abstract The Human Proteome Organization (HUPO) launched the Project (HPP) in 2010, creating an international framework for global collaboration, data sharing, quality assurance and enhancing accurate annotation of genome-encoded proteome. During subsequent decade, HPP established collaborations, developed guidelines metrics, undertook reanalysis previously deposited community data, continuously increasing coverage human On occasion HPP’s tenth anniversary, we here report a 90.4% complete high-stringency proteome blueprint. This knowledge is essential discerning molecular processes health disease, as demonstrate by highlighting potential roles plays our understanding, diagnosis treatment cancers, cardiovascular infectious diseases.

Язык: Английский

Процитировано

195

Integrative Multi-Omics Approaches in Cancer Research: From Biological Networks to Clinical Subtypes DOI Open Access

Yong Jin Heo,

Chanwoong Hwa, Gang‐Hee Lee

и другие.

Molecules and Cells, Год журнала: 2021, Номер 44(7), С. 433 - 443

Опубликована: Июль 1, 2021

Multi-omics approaches are novel frameworks that integrate multiple omics datasets generated from the same patients to better understand molecular and clinical features of cancers.A wide range emerging multiview clustering algorithms now provide unprecedented opportunities further classify cancers into subtypes, improve survival prediction therapeutic outcome these key pathophysiological processes through different layers.In this review, we overview concept rationale multi-omics in cancer research.We also introduce recent advances development integration methods for multiple-layered patients.Finally, summarize latest findings large-scale studies various their implications patient subtyping drug development.

Язык: Английский

Процитировано

149

The next horizon in precision oncology: Proteogenomics to inform cancer diagnosis and treatment DOI Creative Commons
Henry Rodriguez, Jean C. Zenklusen, Louis M. Staudt

и другие.

Cell, Год журнала: 2021, Номер 184(7), С. 1661 - 1670

Опубликована: Апрель 1, 2021

When it comes to precision oncology, proteogenomics may provide better prospects the clinical characterization of tumors, help make a more accurate diagnosis cancer, and improve treatment for patients with cancer. This perspective describes significant contributions The Cancer Genome Atlas Clinical Proteomic Tumor Analysis Consortium oncology makes case that needs be fully integrated into trials patient care in order deliver right cancer at dose time.

Язык: Английский

Процитировано

146

Large-scale and high-resolution mass spectrometry-based proteomics profiling defines molecular subtypes of esophageal cancer for therapeutic targeting DOI Creative Commons
Wei Liu, Lei Xie, Yaohui He

и другие.

Nature Communications, Год журнала: 2021, Номер 12(1)

Опубликована: Авг. 16, 2021

Abstract Esophageal cancer (EC) is a type of aggressive without clinically relevant molecular subtypes, hindering the development effective strategies for treatment. To define subtypes EC, we perform mass spectrometry-based proteomic and phosphoproteomics profiling EC tumors adjacent non-tumor tissues, revealing catalog proteins phosphosites that are dysregulated in ECs. The cohort stratified into two subtypes—S1 S2—based on analysis, with S2 subtype characterized by upregulation spliceosomal ribosomal proteins, being more aggressive. Moreover, identify signature composed ELOA SCAF4, construct diagnostic prognostic model. Potential drugs predicted treating patients subtype, three candidate validated to inhibit EC. Taken together, our analysis thus providing potential therapeutic outlook improving disease outcomes

Язык: Английский

Процитировано

124