Leire Moya

ORCID: 0000-0001-9127-344X
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Research Areas
  • Prostate Cancer Treatment and Research
  • Cancer-related molecular mechanisms research
  • RNA Research and Splicing
  • Genetic Associations and Epidemiology
  • MicroRNA in disease regulation
  • RNA modifications and cancer
  • SARS-CoV-2 and COVID-19 Research
  • Molecular Biology Techniques and Applications
  • Prostate Cancer Diagnosis and Treatment
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Circular RNAs in diseases
  • Management of metastatic bone disease
  • Liver Disease Diagnosis and Treatment
  • Cancer-related gene regulation
  • COVID-19 Clinical Research Studies
  • Legume Nitrogen Fixing Symbiosis
  • Radiopharmaceutical Chemistry and Applications
  • Food composition and properties
  • RNA regulation and disease
  • Immune responses and vaccinations
  • Genomics and Chromatin Dynamics
  • Cancer Cells and Metastasis
  • Hypothalamic control of reproductive hormones
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Garlic and Onion Studies

Queensland University of Technology
2015-2024

Translational Research Institute
2015-2022

Prostate Cancer Research
2014-2018

Plant & Food Research
2013-2017

QIMR Berghofer Medical Research Institute
2015

Universitat Politècnica de València
2013

Hospital Plató
1990-2013

Fredrick R. Schumacher Ali Amin Al Olama Sonja I. Berndt Sara Benlloch Mahbubl Ahmed and 95 more Edward J. Saunders Tokhir Dadaev Daniel Leongamornlert Ezequiel Anokian Clara Cieza-Borrella Chee Goh Mark N. Brook Xin Sheng Laura Fachal Joe Dennis Jonathan P. Tyrer Kenneth Muir Artitaya Lophatananon Victoria L. Stevens Susan M. Gapstur Brian D. Carter Catherine M. Tangen Phyllis J. Goodman Ian M. Thompson Jyotsna Batra Suzanne K. Chambers Leire Moya Judith A. Clements Lisa G. Horvath Wayne D. Tilley Gail P. Risbridger Henrik Grönberg Markus Aly Tobias Nordström Paul D.P. Pharoah Nora Pashayan Johanna Schleutker Teuvo L.J. Tammela Csilla Sipeky Anssi Auvinen Demetrius Albanes Stephanie J. Weinstein Alicja Wolk Niclas Håkansson Catharine West Alison M. Dunning N.G. Burnet Lorelei A. Mucci Edward Giovannucci Gerald L. Andriole Olivier Cussenot Géraldine Cancel‐Tassin Stella Koutros Laura E. Beane Freeman Karina D. Sørensen Torben F. Ørntoft Michael Borre Lovise Mæhle Eli Marie Grindedal David E. Neal Jenny Donovan Freddie C. Hamdy Richard M. Martin Ruth C. Travis Timothy J. Key Robert J. Hamilton Neil E. Fleshner Antonio Finelli Sue A. Ingles Mariana C. Stern Barry S. Rosenstein Sarah L. Kerns Harry Ostrer Yong‐Jie Lu Hong-Wei Zhang Ninghan Feng Xueying Mao Xin Guo Guomin Wang Zan Sun Graham G. Giles Melissa C. Southey Robert J. MacInnis Liesel M. FitzGerald Adam S. Kibel Bettina F. Drake Ana Vega Antonio Gómez‐Caamaño Robert Szulkin Martin Eklund Manolis Kogevinas Javier Llorca Gemma Castaño‐Vinyals Kathryn L. Penney Meir J. Stampfer Jong Y. Park Thomas A. Sellers Hui‐Yi Lin Janet L. Stanford Cezary Cybulski

10.1038/s41588-018-0142-8 article EN Nature Genetics 2018-06-08

Prostate cancer is diagnosed in over 1 million men every year globally, yet current diagnostic modalities are inadequate for identification of significant and more reliable early biomarkers necessary improved clinical management prostate patients. MicroRNAs (miRNAs) modulate important cellular processes/pathways contributing to stably present body fluids. In this study we profiled 372 cancer-associated miRNAs plasma collected before (~60% patients) after/during commencement treatment (~40%...

10.1038/s41598-018-24424-w article EN cc-by Scientific Reports 2018-04-23
Ben Hollis Felix R. Day Alexander S Busch Deborah J. Thompson Ana Luiza G. Soares and 95 more Paul R. H. J. Timmers Alex S. F. Kwong Doug Easton Peter K. Joshi Nicholas J. Timpson Rosalind A. Eeles Brian E. Henderson Christopher A. Haiman Zsofia Kote‐Jarai Fredrick R. Schumacher Ali Amin Al Olama Sara Benlloch Kenneth Muir Sonja I. Berndt David V. Conti Fredrik Wiklund Stephen Chanock Susan M. Gapstur Victoria L. Stevens Catherine M. Tangen Jyotsna Batra Judith A. Clements Wayne D. Tilley Gail P. Risbridger Judith A. Clements Lisa G. Horvath Renea A. Taylor Vanessa M. Hayes Lisa M. Butler Trina Yeadon Allison Eckert Pâmela Saunders Anne‐Maree Haynes Melissa Papargiris Srilakshmi Srinivasan Mary‐Anne Kedda Leire Moya Jyotsna Batra Henrik Grönberg Nora Pashayan Johanna Schleutker Demetrius Albanes Alicja Wolk Catharine West Lorelei A. Mucci Géraldine Cancel‐Tassin Stella Koutros Karina D. Sørensen Eli Marie Grindedal David E. Neal Freddie C. Hamdy Jenny Donovan Ruth C. Travis Robert J. Hamilton Sue A. Ingles Barry S. Rosenstein Yong‐Jie Lu Graham G. Giles Adam S. Kibel Ana Vega Manolis Kogevinas Kathryn L. Penney Jong Y. Park Janet L. Stanford Cezary Cybulski Børge G. Nordestgaard Hermann Brenner Christiane Maier Jeri Kim Esther M. John Manuel R. Teixeira Susan L. Neuhausen Kim De Ruyck Azad Hassan Abdul Razack Lisa F. Newcomb Davor Lessel Radka Kaneva Nawaid Usmani Frank Claessens Paul A. Townsend Manuela Gago‐Dominguez Monique J. Roobol F. Ménégaux Kay-Tee Khaw Lisa Cannon‐Albright Hardev Pandha Stephen N. Thibodeau Michelle Agee Babak Alipanahi Adam Auton Robert K. Bell Katarzyna Bryc Sarah L. Elson Pierre Fontanillas Nicholas A. Furlotte

Abstract The timing of puberty is highly variable and associated with long-term health outcomes. To date, understanding the genetic control based largely on studies in women. Here, we report a multi-trait genome-wide association study for male an effective sample size 205,354 men. We find moderately strong genomic correlation between sexes (rg = 0.68) identify 76 independent signals timing. Implicated mechanisms include unexpected link natural hair colour, possibly reflecting common effects...

10.1038/s41467-020-14451-5 article EN cc-by Nature Communications 2020-03-24

Abstract Background Prostate cancer is a broad-spectrum disease, spanning from indolent to highly aggressive lethal malignancy. cell lines are essential tools understanding the basic features of this malignancy, as well in identifying novel therapeutic strategies. However, most routinely used prostate research derived metastatic disease and may not fully elucidate molecular events underlying early stages development progression. Thus, there need for new localised better span spectrum....

10.1038/s41391-023-00679-x article EN cc-by Prostate Cancer and Prostatic Diseases 2023-06-01

The oncogene MDM4 , also known as MDMX or HDMX contributes to cancer susceptibility and progression through its capacity negatively regulate a range of genes with tumour-suppressive functions. As part recent genome-wide association study it was determined that the A-allele rs4245739 SNP (A>C), located in 3′-UTR is associated an increased risk prostate cancer. Computational predictions revealed within predicted binding site for three microRNAs (miRNAs): miR-191-5p, miR-887 miR-3669....

10.1530/erc-15-0013 article EN Endocrine Related Cancer 2015-02-10
Jodie N. Painter Tracy A. O’Mara Jyotsna Batra Timothy Cheng Felicity Lose and 95 more Joe Dennis Kyriaki Michailidou Jonathan P. Tyrer Shahana Ahmed Kaltin Ferguson Catherine S. Healey Susanne Kaufmann Kristine M. Hillman Carina Walpole Leire Moya Pamela M. Pollock Angela Jones Kimberley Howarth Lynn Martin Maggie Gorman Shirley Hodgson Ma. Magdalena Echeverry de Polanco Mónica Sans Ángel Carracedo Sergi Castellví–Bel Augusto Rojas‐Martínez Érika Maria Monteiro Santos Manuel R. Teixeira Luis G. Carvajal‐Carmona Xiao‐Ou Shu Jirong Long Wei Zheng Yong‐Bing Xiang Grant W. Montgomery Penelope M. Webb Rodney J. Scott Mark McEvoy John Attia Elizabeth Holliday Nicholas G. Martin Dale R. Nyholt Anjali K. Henders Peter A. Fasching Alexander Hein Matthias W. Beckmann Stefan P. Renner Thilo Dörk Peter Hillemanns Matthias Dürst Ingo B. Runnebaum Diether Lambrechts Lieve Coenegrachts Stefanie Schrauwen Frédéric Amant Boris Winterhoff Sean C. Dowdy Ellen L. Goode Attila Teoman Helga B. Salvesen Jone Trovik Tormund S. Njølstad Henrica M.J. Werner Katie A. Ashton Tony Proietto Geoffrey Otton Gerasimos Tzortzatos Miriam Mints Emma Tham Per Hall Kamila Czene Jianjun Liu Jingmei Li John L. Hopper Melissa C. Southey Arif B. Ekici Matthias Ruebner Nicola Johnson Julian Peto Barbara Burwinkel Frederik Marmé Hermann Brenner Aida Karina Dieffenbach Thomas Ind Hiltrud Brauch Annika Lindblom Jeroen Depreeuw Matthieu Moisse Jenny Chang‐Claude Anja Rudolph Fergus J. Couch Janet E. Olson Graham G. Giles Fiona Bruinsma Julie M. Cunningham Brooke L. Fridley Anne‐Lise Børresen‐Dale Vessela N. Kristensen Angela Cox Anthony J. Swerdlow Nick Orr

Common variants in the hepatocyte nuclear factor 1 homeobox B (HNF1B) gene are associated with risk of Type II diabetes and multiple cancers. Evidence to date indicates that cancer may be mediated via genetic or epigenetic effects on HNF1B expression. We previously found single-nucleotide polymorphisms (SNPs) at locus endometrial cancer, now report extensive fine-mapping silico laboratory analyses this locus. Analysis 1184 genotyped imputed SNPs 6608 Caucasian cases 37 925 controls, 895...

10.1093/hmg/ddu552 article EN Human Molecular Genetics 2014-11-06
Marco Matejcic Edward J. Saunders Tokhir Dadaev Mark N. Brook Kan Wang and 95 more Xin Sheng Ali Amin Al Olama Fredrick R. Schumacher Sue A. Ingles Koveela Govindasami Sara Benlloch Sonja I. Berndt Demetrius Albanes Stella Koutros Kenneth Muir Victoria L. Stevens Susan M. Gapstur Catherine M. Tangen Jyotsna Batra Judith A. Clements Henrik Grönberg Nora Pashayan Johanna Schleutker Alicja Wolk Catharine West Lorelei A. Mucci Peter Kraft Géraldine Cancel‐Tassin Karina D. Sørensen Lovise Mæhle Eli Marie Grindedal Sara S. Strom David E. Neal Freddie C. Hamdy Jenny Donovan Ruth C. Travis Robert J. Hamilton Barry S. Rosenstein Yong‐Jie Lu Graham G. Giles Adam S. Kibel Ana Vega J.T. Bensen Manolis Kogevinas Kathryn L. Penney Jong Y. Park Janet L. Stanford Cezary Cybulski Børge G. Nordestgaard Hermann Brenner Christiane Maier Jeri Kim Manuel R. Teixeira Susan L. Neuhausen Kim De Ruyck Azad Hassan Abdul Razack Lisa F. Newcomb Davor Lessel Radka Kaneva Nawaid Usmani Frank Claessens Paul A. Townsend Manuela Gago‐Dominguez Monique J. Roobol F. Ménégaux Kay‐Tee Khaw Lisa Cannon‐Albright Hardev Pandha Stephen N. Thibodeau Daniel J. Schaid B. E. Henderson Mariana C. Stern Alison Thwaites Michelle Guy Ian Whitmore Angela Morgan Cyril Fisher Steve Hazel Naomi Livni Margaret Cook Laura Fachal Stephanie J. Weinstein Laura E. Beane Freeman Robert N. Hoover Mitchell J. Machiela Artitaya Lophatananon Brian D. Carter Phyllis J. Goodman Leire Moya Srilakshmi Srinivasan Mary‐Anne Kedda Trina Yeadon Allison Eckert Martin Eklund Carin Cavalli-Bjoerkman Alison M. Dunning Csilla Sipeky Niclas Håkansson Rebecca Elliott Hardeep Ranu

Abstract Chromosome 8q24 is a susceptibility locus for multiple cancers, including prostate cancer. Here we combine genetic data across the region from 71,535 cancer cases and 52,935 controls of European ancestry to define overall contribution germline variation at risk. We identify 12 independent risk signals ( p < 4.28 × 10 −15 ), three variants that have yet be reported. From polygenic score (PRS) model, derived assess cumulative effect 8q24, men in top 1% PRS 4-fold (95%CI =...

10.1038/s41467-018-06863-1 article EN cc-by Nature Communications 2018-10-30

Although starch consists of large macromolecules composed glucose units linked by α-1,4-glycosidic linkages with α-1,6-glycosidic branchpoints, variation in structural and functional properties is found both within between species. Interest genetics based on the importance food industrial processes, potential to provide novel starches. The metabolic pathway complex but has been characterized diverse plant species, including pea. To understand how allelic pea affects structure percent...

10.1186/s12870-017-1080-9 article EN cc-by BMC Plant Biology 2017-08-01
Srilakshmi Srinivasan Thomas Kryza Nathalie Bock Brian Wan-Chi Tse Kamil A. Sokolowski and 95 more Janaththani Panchadsaram Achala Fernando Leire Moya Carson Stephens Ying Dong Joan Röhl Saeid Alinezhad Ian Vela Joanna Perry‐Keene Katie Buzacott Robert Nica Elizabeth Bancroft Elizabeth Page Audrey Ardern‐Jones Chris Bangma Elena Castro David P. Dearnaley Diana Eccles D. Gareth Evans Jórunn E. Eyfjörd Alison Falconer Christopher S. Foster Freddie C. Hamdy Óskar Þór Jóhannsson Vincent Khoo Geoffrey J. Lindeman Jan Lubiński Lovise Mæhle A. Millner Christos Mikropoulos Anita Mitra Clare Moynihan Judith Offman Gad Rennert Lucy Side Mohnish Suri Penny Wilson Manuela Gago‐Dominguez Pardeep Kumar Antonis C. Antoniou Jana McHugh Holly Ní Raghallaigh R. R. Hall Natalie Taylor Sarah Thomas Kathryn Myhill Matthew Hogben Eva McGrowder Diana Keating Denzil James Jacob Merson Syed Arshad Hussain Angela Wood Nening M. Dennis Paul Ardern-Jones N. van As Steve Hazell Sarah J. Lewis Paul D.P. Pharoah J. Schalken Aslam Sohaib Nandita de Souza Paul Cathcart Frank Chingewundoh Michael C. Perry Jeff Bamber Alexander Dias Christos Mikropolis Sibel Saya Anthony Chamberlain Anne-Marie Borges Da Silva Lucia D’Mello Sue Moss J Melia Netty Kinsella Justyna Sobczak Naami Mcaddy David Nicol Chris Ogden Declan Cahill Alan Thompson Christopher Woodhouse Vincent J. Gnanapragasam Colin Cooper Jeremy Clark Johanna Schleutker Christiane Maier Kenneth Muir Catherine M. Tangen Henrik Grönberg Nora Pashayan Demetrius Albanes Alicja Wolk Janet L. Stanford S.I. Berndt

Abstract Genetic variation at the 19q13.3 KLK locus is linked with prostate cancer susceptibility in men. The non-synonymous KLK3 single nucleotide polymorphism (SNP), rs17632542 (c.536 T > C; Ile163Thr-substitution PSA) associated reduced risk, however, functional relevance unknown. Here, we identify that SNP variant-induced change PSA biochemical activity mediates pathogenesis. ‘Thr’ variant leads to small subcutaneous tumours, supporting risk. However, also displays higher metastatic...

10.1038/s41467-024-52472-6 article EN cc-by Nature Communications 2024-11-06

Fusion transcripts are found in many tissues and have the potential to create novel functional products. Here, we investigate genomic sequences around fusion junctions better understand transcriptional mechanisms mediating transcription/splicing. We analyzed data from prostate (cancer) cells as previous studies shown extensively that these readily undergo transcription.We used FusionMap program identify high-confidence RNAseq data. The datasets were our (N = 8) other 14) clinical tumors with...

10.1186/s12864-015-2235-4 article EN cc-by BMC Genomics 2015-12-01

Short tandem repeats (STRs) are repetitive sequences of a polymorphic stretch two to six nucleotides. We hypothesized that STRs associated with prostate cancer development and/or progression. undertook RNA sequencing analysis tumors and adjacent non-malignant cells identify readily expressed in these cells. Most the clinical samples mapped intronic intergenic DNA. Our indicated three (TAAA-ACTG2, TTTTG-TRIB1, TG-PCA3) differentially compared TG-PCA3 STR expression was repressed by...

10.1038/s41598-017-16700-y article EN cc-by Scientific Reports 2017-11-28

With an estimated 1.1 million men worldwide diagnosed with prostate cancer yearly, effective and more specific biomarkers for early diagnosis could lead to better treatments. As such, novel genetic markers are sought this purpose. The tribbles homologue 1 gene (TRIB1) has recently shown have a role in tumorigenesis oncomine data-mining confirmed clinical significance of TRIB1 cancer. For the first time, polymorphic microsatellite been studied its potential association risk aggressiveness....

10.3389/fgene.2018.00428 article EN cc-by Frontiers in Genetics 2018-10-04
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