4.6 Review

DNA methylation biomarkers in biological fluids for early detection of respiratory tract cancer

Journal

CLINICAL CHEMISTRY AND LABORATORY MEDICINE
Volume 50, Issue 10, Pages 1723-1731

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/cclm-2012-0124

Keywords

biomarkers; DNA methylation; lung cancer; oral cancer

Ask authors/readers for more resources

Cancers of the respiratory tract (lung and head and neck) share common aetiologies, risk factors and molecular characteristics. Epigenetic reprogramming is one of the hallmarks of cancer and DNA methylation is currently the best-studied form. There are a number of characteristics of DNA methylation, which seem advantageous in biomarker development. Early detection is still an unmet clinical care need, which guarantees to significantly reduce the mortality of patients with respiratory cancers. The application of such biomarkers in biological fluids being sampled in everyday clinical practice is a long-term demand. In this review we summarise the current literature on DNA methylation detection in bronchial washings, sputum, saliva, plasma and serum and discuss the potential of their clinical implementation. We also discuss important aspects of biomarker development and validation pointing to the appropriate route for a biomarker to reach clinical standards.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Oncology

Long non-coding RNA dysregulation is a frequent event in non-small cell lung carcinoma pathogenesis

Amelia Acha-Sagredo, Bubaraye Uko, Paschalia Pantazi, Naiara G. Bediaga, Chryssanthi Moschandrea, Lucille Rainbow, Michael W. Marcus, Michael P. A. Davies, John K. Field, Triantafillos Liloglou

BRITISH JOURNAL OF CANCER (2020)

Article Oncology

Overexpression of HURP mRNA in head and neck carcinoma and association with in vitro response to vinorelbine

Ahmed S. K. Al-Khafaji, Paschalia Pantazi, Amelia Acha-Sagredo, Andrew Schache, Janet M. Risk, Richard J. Shaw, Triantafillos Liloglou

ONCOLOGY LETTERS (2020)

Article Oncology

Fibroblasts from Distinct Pancreatic Pathologies Exhibit Disease-Specific Properties

Lawrence N. Barrera, Anthony Evans, Brian Lane, Sarah Brumskill, Frances E. Oldfield, Fiona Campbell, Timothy Andrews, Zipeng Lu, Pedro A. Perez-Mancera, Triantafillos Liloglou, Milton Ashworth, Mehdi Jalali, Rebecca Dawson, Quentin Nunes, Phoebe A. Phillips, John F. Timms, Christopher Halloran, William Greenhalf, John P. Neoptolemos, Eithne Costello

CANCER RESEARCH (2020)

Article Biochemistry & Molecular Biology

Low protein intake during reproduction compromises the recovery of lactation-induced bone loss in female mouse dams without affecting skeletal muscles

Ioannis Kanakis, Moussira Alameddine, Mattia Scalabrin, Rob J. van't Hof, Triantafillos Liloglou, Susan E. Ozanne, Katarzyna Goljanek-Whysall, Aphrodite Vasilaki

FASEB JOURNAL (2020)

Review Biochemistry & Molecular Biology

Balancing neurotrophin pathway and sortilin function: Its role in human disease

Minnatallah Al-Yozbaki, Amelia Acha-Sagredo, Alex George, Triantafillos Liloglou, Cornelia M. Wilson

BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER (2020)

Article Hematology

TLR9 expression in chronic lymphocytic leukemia identifies a promigratory subpopulation and novel therapeutic target

Emma Kennedy, Eve Coulter, Emma Halliwell, Nuria Profitos-Peleja, Elisabeth Walsby, Barnaby Clark, Elizabeth H. Phillips, Thomas A. Burley, Simon Mitchell, Stephen Devereux, Christopher D. Fegan, Christopher Jones, Rosalynd Johnston, Tim Chevassut, Ralph Schulz, Martina Seiffert, Angelo Agathanggelou, Ceri Oldreive, Nicholas Davies, Tatjana Stankovic, Triantafillos Liloglou, Chris Pepper, Andrea G. S. Pepper

Summary: Despite the advancements in B-cell receptor-targeted inhibitors, CLL remains incurable. TLR9 activation by unmethylated DNA is associated with disease progression in CLL. High TLR9 expression promotes CLL cell migration and disease progression, while dual targeting of TLR9 and BTK shows strong synergism as a potential treatment strategy for this incurable disease.

BLOOD (2021)

Article Oncology

Rare deleterious germline variants and risk of lung cancer

Yanhong Liu, Jun Xia, James McKay, Spiridon Tsavachidis, Xiangjun Xiao, Margaret R. Spitz, Chao Cheng, Jinyoung Byun, Wei Hong, Yafang Li, Dakai Zhu, Zhuoyi Song, Susan M. Rosenberg, Michael E. Scheurer, Farrah Kheradmand, Claudio W. Pikielny, Christine M. Lusk, Ann G. Schwartz, Ignacio I. Wistuba, Michael H. Cho, Edwin K. Silverman, Joan Bailey-Wilson, Susan M. Pinney, Marshall Anderson, Elena Kupert, Colette Gaba, Diptasri Mandal, Ming You, Mariza de Andrade, Ping Yang, Triantafillos Liloglou, Michael P. A. Davies, Jolanta Lissowska, Beata Swiatkowska, David Zaridze, Anush Mukeria, Vladimir Janout, Ivana Holcatova, Dana Mates, Jelena Stojsic, Ghislaine Scelo, Paul Brennan, Geoffrey Liu, John K. Field, Rayjean J. Hung, David C. Christiani, Christopher I. Amos

Summary: Recent studies indicate that rare variants could have a significant impact on the etiology of lung cancers. Through comprehensive sequencing, rare deleterious variants associated with lung cancer susceptibility were identified, including both known and novel susceptibility genes. Further mechanistic studies are needed to evaluate the pathogenic effects of these specific alleles.

NPJ PRECISION ONCOLOGY (2021)

Article Multidisciplinary Sciences

A long intergenic non-coding RNA regulates nuclear localization of DNA methyl transferase-1

Rhian Jones, Susanne Wijesinghe, Claire Wilson, John Halsall, Triantafillos Liloglou, Aditi Kanhere

Summary: The nuclear lincRNA CCDC26 plays a crucial role in regulating DNMT1 activity and controlling DNA methylation levels. Its absence leads to mis-localization of DNMT1 to the cytoplasm, causing significant hypomethylation of genomic DNA, double-stranded DNA breaks, and increased cell death. This study reveals a previously unrecognized mechanism of lincRNA-mediated subcellular localization of DNMT1 and regulation of DNA methylation.

ISCIENCE (2021)

Article Medicine, Research & Experimental

SAVER: sodium valproate for the epigenetic reprogramming of high-risk oral epithelial dysplasia-a phase II randomised control trial study protocol

Caroline McCarthy, Joseph Sacco, Stefano Fedele, Michael Ho, Stephen Porter, Triantafillos Liloglou, Bill Greenhalf, Max Robinson, Bridget Young, Silvia Cicconi, Seema Chauhan, Binyam Tesfaye, Richard Jackson, Frances Sherratt, Richard Shaw

Summary: The SAVER trial aims to investigate the potential chemopreventive effects of VPA in patients with high-risk OED, while assessing the feasibility and acceptability of the trial.

TRIALS (2021)

Article Biochemical Research Methods

Iam hiQ-a novel pair of accuracy indices for imputed genotypes

Albert Rosenberger, Viola Tozzi, Heike Bickeboeller

Summary: This paper introduces an independent pair of accuracy measures, Iam hiQ, which can be applied to evaluate the output of all imputation software; by applying both measures to a large sample of the International Lung Cancer Consortium (ILCCO), meaningful thresholds for classifying markers of poor accuracy were found.

BMC BIOINFORMATICS (2022)

Article Oncology

Genetic variants associated with mandibular osteoradionecrosis following radiotherapy for head and neck malignancy

Rachel C. Brooker, Philipp Antczak, Triantafillos Liloglou, Janet M. Risk, Joseph J. Sacco, Andrew G. Schache, Richard J. Shaw

Summary: This study identified a panel of genetic variants that can predict mandibular osteoradionecrosis (ORN) in head and neck cancer patients, offering new insight into personalized radiotherapy strategies for ORN management. The model developed achieved 92% accuracy and four SNPs were significantly associated with the absence of ORN, potentially guiding patient selection for personalized radiotherapy.

RADIOTHERAPY AND ONCOLOGY (2021)

Article Cell Biology

Variable allelic expression of imprinted genes at the Peg13, Trappc9, Ago2 cluster in single neural cells

Michael Claxton, Michela Pulix, Michelle K. Y. Seah, Ralph Bernardo, Peng Zhou, Sultan Aljuraysi, Triantafillos Liloglou, Philippe Arnaud, Gavin Kelsey, Daniel M. Messerschmidt, Antonius Plagge

Summary: Genomic imprinting is an epigenetic process that leads to parent-of-origin specific gene expression. In this study, the researchers investigated the allelic expression biases in the brain and found variable states of allelic expression, especially for Trappc9 and Ago2 genes. They also discovered that Trappc9 and Ago2 are not imprinted in hippocampus-derived neural stem cells. The findings suggest the presence of variability and mosaicism in allelic expression between individual cells of the brain tissue.

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2022)

Article Medicine, General & Internal

Plasma protein biomarkers for early prediction of lung cancer

Michael P. A. Davies, Takahiro Sato, Haitham Ashoor, Liping Hou, Triantafillos Liloglou, Robert Yang, John K. Field

Summary: The study investigated the potential of plasma proteomes for lung cancer prediction and identified differentially expressed proteins and pathways associated with the presence and prediction of lung cancer.

EBIOMEDICINE (2023)

Article Medicine, Research & Experimental

Gene-gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer

Albert Rosenberger, Nils Muttray, Rayjean J. Hung, David C. Christiani, Neil E. Caporaso, Geoffrey Liu, Stig E. Bojesen, Loic Le Marchand, Demetrios Albanes, Melinda C. Aldrich, Adonina Tardon, Guillermo Fernandez-Tardon, Gad Rennert, John K. Field, Michael P. A. Davies, Triantafillos Liloglou, Lambertus A. Kiemeney, Philip Lazarus, Bernadette Wendel, Aage Haugen, Shanbeh Zienolddiny, Stephen Lam, Matthew B. Schabath, Angeline S. Andrew, Eric J. Duell, Susanne M. Arnold, Gary E. Goodman, Chu Chen, Jennifer A. Doherty, Fiona Taylor, Angela Cox, Penella J. Woll, Angela Risch, Thomas R. Muley, Mikael Johansson, Paul Brennan, Maria Teresa Landi, Sanjay S. Shete, Christopher Amos, Heike Bickeboeller

Summary: This study assessed the association and predictive ability of AhR/Wnt genes with lung cancer in individuals of European descent. The results showed no genome-wide significant association with overall lung cancer, but significant associations were observed in subgroups of ever smokers and never smokers. Although the predictability is poor, AhR/Wnt variants are overrepresented in optimized prediction scores for lung cancer.

EUROPEAN JOURNAL OF MEDICAL RESEARCH (2022)

Article Oncology

Activating transcription factor-2 (ATF2) is a key determinant of resistance to endocrine treatment in an in vitro model of breast cancer

Athina Giannoudis, Mohammed Imad Malki, Bharath Rudraraju, Hisham Mohhamed, Suraj Menon, Triantafillos Liloglou, Simak Ali, Jason S. Carroll, Carlo Palmieri

BREAST CANCER RESEARCH (2020)

No Data Available