Epitranscriptomics and epiproteomics in cancer drug resistance: therapeutic implications DOI Creative Commons

Huibin Song,

Dongcheng Liu, Shaowei Dong

и другие.

Signal Transduction and Targeted Therapy, Год журнала: 2020, Номер 5(1)

Опубликована: Сен. 8, 2020

Abstract Drug resistance is a major hurdle in cancer treatment and key cause of poor prognosis. Epitranscriptomics epiproteomics are crucial cell proliferation, migration, invasion, epithelial–mesenchymal transition. In recent years, epitranscriptomic epiproteomic modification has been investigated on their roles overcoming drug resistance. this review article, we summarized the progress three novel aspects: (i) mRNA modification, which includes alternative splicing, A-to-I methylation; (ii) noncoding RNAs involves miRNAs, lncRNAs, circRNAs; (iii) posttranslational molecules encompasses inactivation/efflux, target modifications, DNA damage repair, death resistance, EMT, metastasis. addition, discussed therapeutic implications targeting some classical chemotherapeutic drugs such as cisplatin, 5-fluorouridine, gefitinib via these modifications. Taken together, highlights importance provides new insights potential targets to reverse

Язык: Английский

Next-generation characterization of the Cancer Cell Line Encyclopedia DOI
Mahmoud Ghandi, Franklin W. Huang, Judit Jané‐Valbuena

и другие.

Nature, Год журнала: 2019, Номер 569(7757), С. 503 - 508

Опубликована: Май 1, 2019

Язык: Английский

Процитировано

2794

Single-Cell RNA-Seq Technologies and Related Computational Data Analysis DOI Creative Commons
Geng Chen, Baitang Ning, Tieliu Shi

и другие.

Frontiers in Genetics, Год журнала: 2019, Номер 10

Опубликована: Апрель 5, 2019

Single-cell RNA sequencing (scRNA-seq) technologies allow the dissection of gene expression at single-cell resolution, which greatly revolutionizes transcriptomic studies. A number scRNA-seq protocols have been developed, and these methods possess their unique features with distinct advantages disadvantages. Due to technical limitations biological factors, data are noisier more complex than bulk RNA-seq data. The high variability raises computational challenges in analysis. Currently, although an increasing bioinformatics proposed for analyzing interpreting data, novel algorithms required ensure accuracy reproducibility results. In this review, we provide overview currently available isolation technologies, discuss diverse analyses including quality control, read mapping, quantification, batch effect correction, normalization, imputation, dimensionality reduction, feature selection, cell clustering, trajectory inference, differential calling, alternative splicing, allelic regulatory network reconstruction. Further, outline prospective development applications technologies.

Язык: Английский

Процитировано

817

Roles and mechanisms of alternative splicing in cancer — implications for care DOI
Sophie Bonnal, Irene López‐Oreja, Juan Valcárcel

и другие.

Nature Reviews Clinical Oncology, Год журнала: 2020, Номер 17(8), С. 457 - 474

Опубликована: Апрель 17, 2020

Язык: Английский

Процитировано

560

Selective degradation of splicing factor CAPERα by anticancer sulfonamides DOI

Taisuke Uehara,

Yukinori Minoshima, Koji Sagane

и другие.

Nature Chemical Biology, Год журнала: 2017, Номер 13(6), С. 675 - 680

Опубликована: Апрель 24, 2017

Язык: Английский

Процитировано

331

Electrochemical biosensors for the detection of lung cancer biomarkers: A review DOI
Akbar Khanmohammadi,

Ali B.G. Aghaie,

Ensieh Vahedi

и другие.

Talanta, Год журнала: 2019, Номер 206, С. 120251 - 120251

Опубликована: Авг. 10, 2019

Язык: Английский

Процитировано

306

EMT and stemness: flexible processes tuned by alternative splicing in development and cancer progression DOI Creative Commons
Davide Pradella, Chiara Naro, Claudio Sette

и другие.

Molecular Cancer, Год журнала: 2017, Номер 16(1)

Опубликована: Янв. 13, 2017

Epithelial-to-mesenchymal transition (EMT) is associated with metastasis formation as well generation and maintenance of cancer stem cells. In this way, EMT contributes to tumor invasion, heterogeneity chemoresistance. Morphological functional changes involved in these processes require robust reprogramming gene expression, which only partially accomplished at the transcriptional level. Alternative splicing another essential layer expression regulation that expands cell proteome. This step post-transcriptional tightly controls identity between epithelial mesenchymal states during differentiation. Importantly, dysregulation factor function cancer-specific isoform frequently occurs human tumors, suggesting importance alternative for biology. review, we briefly discuss role programs development, differentiation progression. Next, focus on selected examples key factors are regulated post-transcriptionally through mechanisms. Lastly, describe relevant oncogenic splice-variants directly orchestrate biology EMT, may be envisioned novel targets therapeutic intervention.

Язык: Английский

Процитировано

272

Metals and Mechanisms of Carcinogenesis DOI Open Access
Qiao Yi Chen,

Thomas L. DesMarais,

Max Costa

и другие.

The Annual Review of Pharmacology and Toxicology, Год журнала: 2019, Номер 59(1), С. 537 - 554

Опубликована: Янв. 6, 2019

Metal exposure is pervasive and not limited to sporadic poisoning events or toxic waste sites. Hundreds of millions people around the globe are affected by chronic metal exposure, which associated with serious health concerns, including cancer, as demonstrated in a variety studies at molecular, systemic, epidemiologic levels. Metal-induced toxicity carcinogenicity sophisticated complex nature. This review provides broad context holistic view currently available on mechanisms metal-induced carcinogenesis. Specifically, we focus five most prevalent carcinogenic metals, arsenic, nickel, cadmium, chromium, beryllium, their potential drive carcinogenesis humans. A comprehensive understanding behind development cancer can provide valuable insights for therapeutic intervention involving molecular targets

Язык: Английский

Процитировано

271

Transcriptome Profiling in Human Diseases: New Advances and Perspectives DOI Open Access
Amelia Casamassimi, Antonio Federico, Monica Rienzo

и другие.

International Journal of Molecular Sciences, Год журнала: 2017, Номер 18(8), С. 1652 - 1652

Опубликована: Июль 29, 2017

In the last decades, transcriptome profiling has been one of most utilized approaches to investigate human diseases at molecular level. Through expression studies, many biomarkers and therapeutic targets have found for several pathologies. This number is continuously increasing thanks total RNA sequencing. Indeed, this new technology completely revolutionized analysis allowing quantification gene levels allele-specific in a single experiment, as well identify novel genes, splice isoforms, fusion transcripts, world non-coding an unprecedented sequencing also employed important projects, like ENCODE (Encyclopedia regulatory elements) TCGA (The Cancer Genome Atlas), provide snapshot dozens cell lines thousands primary tumor specimens. Moreover, these studies paved way development data integration order facilitate management disease markers use clinics. scenario, ongoing clinical trials utilize through strategies instrument diagnosis numerous

Язык: Английский

Процитировано

238

The Landscape of Isoform Switches in Human Cancers DOI
Kristoffer Vitting‐Seerup, Albin Sandelin

Molecular Cancer Research, Год журнала: 2017, Номер 15(9), С. 1206 - 1220

Опубликована: Июнь 6, 2017

Alternative usage of transcript isoforms from the same gene has been hypothesized as an important feature in cancers. However, differential transcripts between conditions (isoform switching) not comprehensively characterized and across cancer types. To this end, we developed methods for identification visualization isoform switches with predicted functional consequences. Using these methods, switching RNA-seq data >5,500 patients covering 12 solid Isoform potential consequences were common, affecting approximately 19% multiple genes. Among these, leading to loss DNA sequence encoding protein domains more frequent than expected, particularly pancancer switches. We identified several powerful biomarkers: 31 highly predictive patient survival independent Our constitute resource researchers, available through interactive web tools. Moreover, our R package, enable systematic analysis other datasets.Implications: This study indicates that are common dysfunctional cells, which turn means expression should be analyzed at level. Visual Overview: http://mcr.aacrjournals.org/content/molcanres/15/9/1206/F1.large.jpg.Mol Cancer Res; 15(9); 1206-20. ©2017 AACR.

Язык: Английский

Процитировано

226

Phase Separation as a Missing Mechanism for Interpretation of Disease Mutations DOI Creative Commons
Brian Tsang, Iva Pritišanac, Stephen W. Scherer

и другие.

Cell, Год журнала: 2020, Номер 183(7), С. 1742 - 1756

Опубликована: Дек. 1, 2020

Язык: Английский

Процитировано

221