[HTML][HTML] Salivary biomarkers for oral squamous cell carcinoma diagnosis and follow-up: current status and perspectives

M Cristaldi, R Mauceri, O Di Fede, G Giuliana… - Frontiers in …, 2019 - frontiersin.org
Oral cancer is the sixth most common cancer type in the world, and 90% of it is represented
by oral squamous cell carcinoma (OSCC). Despite progress in preventive and therapeutic …

[HTML][HTML] Advances in deubiquitinating enzyme inhibition and applications in cancer therapeutics

AM Antao, A Tyagi, KS Kim, S Ramakrishna - Cancers, 2020 - mdpi.com
Since the discovery of the ubiquitin proteasome system (UPS), the roles of ubiquitinating
and deubiquitinating enzymes (DUBs) have been widely elucidated. The ubiquitination of …

Stem cell divisions, somatic mutations, cancer etiology, and cancer prevention

C Tomasetti, L Li, B Vogelstein - Science, 2017 - science.org
Cancers are caused by mutations that may be inherited, induced by environmental factors,
or result from DNA replication errors (R). We studied the relationship between the number of …

Identification of a variety of mutations in cancer predisposition genes in patients with suspected Lynch syndrome

MB Yurgelun, B Allen, RR Kaldate, KR Bowles… - Gastroenterology, 2015 - Elsevier
Background & Aims Multigene panels are commercially available tools for hereditary cancer
risk assessment that allow for next-generation sequencing of numerous genes in parallel …

Current challenges and new opportunities for gene-environment interaction studies of complex diseases

K McAllister, LE Mechanic, C Amos… - American journal of …, 2017 - academic.oup.com
Recently, many new approaches, study designs, and statistical and analytical methods have
emerged for studying gene-environment interactions (G× Es) in large-scale studies of …

Genetics, genomics, and cancer risk assessment: state of the art and future directions in the era of personalized medicine

JN Weitzel, KR Blazer, DJ MacDonald… - CA: a cancer journal …, 2011 - Wiley Online Library
Scientific and technologic advances are revolutionizing our approach to genetic cancer risk
assessment, cancer screening and prevention, and targeted therapy, fulfilling the promise of …

[HTML][HTML] An optimized prediction framework to assess the functional impact of pharmacogenetic variants

Y Zhou, S Mkrtchian, M Kumondai… - The …, 2019 - nature.com
Prediction of phenotypic consequences of mutations constitutes an important aspect of
precision medicine. Current computational tools mostly rely on evolutionary conservation …

Cancer genomics and inherited risk

ZK Stadler, KA Schrader, J Vijai… - Journal of clinical …, 2014 - ascopubs.org
Next-generation sequencing (NGS) has enabled whole-exome and whole-genome
sequencing of tumors for causative mutations, allowing for more accurate targeting of …

Statistical methods for genome-wide association studies

MH Wang, HJ Cordell, K Van Steen - Seminars in cancer biology, 2019 - Elsevier
Genome-wide association studies (GWAS) detect common genetic variants associated with
complex disorders. With their comprehensive coverage of common single nucleotide …

[HTML][HTML] Association between PD-1 and PD-L1 Polymorphisms and the Risk of Cancer: A Meta-Analysis of Case-Control Studies

M Hashemi, S Karami, S Sarabandi, A Moazeni-Roodi… - Cancers, 2019 - mdpi.com
A number of case-control studies regarding the association of the polymorphisms in the
programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) genes with …