Marit Muri Holmen

ORCID: 0000-0003-2803-4117
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Research Areas
  • Breast Cancer Treatment Studies
  • Cancer Genomics and Diagnostics
  • BRCA gene mutations in cancer
  • Cancer Treatment and Pharmacology
  • Cancer Cells and Metastasis
  • Genetic factors in colorectal cancer
  • Genetic Associations and Epidemiology
  • Genomic variations and chromosomal abnormalities
  • Radiomics and Machine Learning in Medical Imaging
  • Global Cancer Incidence and Screening
  • Cancer-related Molecular Pathways
  • Cancer Risks and Factors
  • Colorectal Cancer Treatments and Studies
  • AI in cancer detection
  • Digital Radiography and Breast Imaging
  • Advanced Biosensing Techniques and Applications
  • Cancer-related molecular mechanisms research
  • Molecular Biology Techniques and Applications
  • Nutrition, Genetics, and Disease
  • Advanced Breast Cancer Therapies
  • Ovarian cancer diagnosis and treatment
  • Breast Lesions and Carcinomas
  • Cancer Immunotherapy and Biomarkers
  • Single-cell and spatial transcriptomics
  • RNA modifications and cancer

Oslo University Hospital
2013-2022

University of Oslo
2021

Norwegian Cancer Society
2004

To explore the predictive value of MRI parameters and tumour characteristics before neoadjuvant chemotherapy (NAC) to compare changes in size apparent diffusion coefficient (ADC) during treatment, between patients who achieved pathological complete response (pCR) those did not. Approval by Regional Ethics Committee written informed consent were obtained. Thirty-one with invasive breast carcinoma scheduled for NAC enrolled (mean age, 50.7; range, 37–72). Study design included treatment (Tp0),...

10.1007/s00330-010-2020-3 article EN cc-by-nc European Radiology 2010-12-02

The addition of annual MRI screening to mammography has heightened optimism that intensive along with improved treatments may substantially improve life expectancy women at high risk breast cancer. However, survival data from BRCA2 mutation carriers undergoing combined are scarce. We have collated the results either or in female Manchester and Oslo use a control group who had their first cancer diagnosed without screening. Eighty-seven undergone (n = 34) 53) compared 274 such Ten year...

10.1186/s13053-016-0048-3 article EN cc-by Hereditary Cancer in Clinical Practice 2016-04-14
Thomas U. Ahearn Haoyu Zhang Kyriaki Michailidou Roger L. Milne Manjeet K. Bolla and 95 more Joe Dennis Alison M. Dunning Michael Lush Qin Wang Irene L. Andrulis Hoda Anton‐Culver Volker Arndt Kristan J. Aronson Paul L. Auer Annelie Augustinsson Adinda Baten Heiko Becher Sabine Behrens Javier Benı́tez Marina Bermisheva Carl Blomqvist Stig E. Bojesen Bernardo Bonanni Anne‐Lise Børresen‐Dale Hiltrud Brauch Hermann Brenner Angela Brooks‐Wilson Thomas Brüning Barbara Burwinkel Saundra S. Buys Federico Canzian Jose E. Castelao Jenny Chang‐Claude Stephen J. Chanock Georgia Chenevix‐Trench Christine L. Clarke Kristine Kleivi Sahlberg Lars Ottestad Rolf Kåresen Ellen Schlichting Marit Muri Holmen Toril Sauer Vilde Drageset Haakensen Olav Engebråten Bjørn Naume Alexander Fosså Cecile E. Kiserud Kristin V. Reinertsen Åslaug Helland Margit Riis Jürgen Geisler J. Margriet Collée Angela Cox Simon S. Cross Kamila Czene Mary B. Daly Peter Devilee Thilo Dörk Miriam Dwek Diana Eccles D. Gareth Evans Peter A. Fasching Jonine D. Figueroa Giuseppe Floris Manuela Gago‐Dominguez Susan M. Gapstur José Á. García-Sáenz Mia M. Gaudet Graham G. Giles Mark S. Goldberg Anna González‐Neira Grethe I.G. Alnæs Mervi Grip Pascal Guénel Christopher A. Haiman Per Hall Ute Hamann Elaine F. Harkness Bernadette A. M. Heemskerk‐Gerritsen Bernd Holleczek Antoinette Hollestelle Maartje J. Hooning Robert N. Hoover John L. Hopper Anthony Howell Christine L. Clarke Rosemary L. Balleine Robert C. Baxter Stephen Braye Jane Carpenter Jane E. Dahlstrom John Forbes CSoon Lee Deborah J. Marsh Adrienne Morey Nirmala Pathmanathan Rodney J. Scott Peter T. Simpson Allan D. Spigelman Nicholas Wilcken

Abstract Background Genome-wide association studies (GWAS) have identified multiple common breast cancer susceptibility variants. Many of these variants differential associations by estrogen receptor (ER) status, but how relate with other tumor features and intrinsic molecular subtypes is unclear. Methods Among 106,571 invasive cases 95,762 controls European ancestry data on 173 in previous GWAS, we used novel two-stage polytomous logistic regression models to evaluate relation (ER,...

10.1186/s13058-021-01484-x article EN cc-by Breast Cancer Research 2022-01-04

Purpose: Chemotherapy-induced alterations to gene expression are due transcriptional reprogramming of tumor cells or subclonal adaptations treatment. The effect on whole-transcriptome mRNA was investigated in a randomized phase II clinical trial assess the neoadjuvant chemotherapy with addition bevacizumab.Experimental Design: Tumor biopsies and profiles were obtained at three fixed time points 66 patients each arm. Altogether, 358 specimens from 132 available, representing state before...

10.1158/1078-0432.ccr-17-0160 article EN Clinical Cancer Research 2017-05-10

Mammographic density (MD), as assessed from film screen mammograms, is determined by the relative content of adipose, connective and epithelial tissue in female breast. In epidemiological studies, a high percentage MD confers four to six fold risk elevation developing breast cancer, even after adjustment for other known cancer factors. However, biologic correlates are little known. Gene expression analysis using whole genome arrays was performed on biopsies 143 women; 79 women with no...

10.1186/bcr2632 article EN cc-by Breast Cancer Research 2010-08-01

Abstract Background Increased understanding of the variability in normal breast biology will enable us to identify mechanisms cancer initiation and origin different subtypes, better predict risk. Methods Gene expression patterns biopsies from 79 healthy women referred diagnostic centers Norway were explored by unsupervised hierarchical clustering supervised analyses, such as gene set enrichment analysis ontology comparison with previously published genelists independent datasets. Results...

10.1186/1755-8794-4-77 article EN cc-by BMC Medical Genomics 2011-11-01

Although systemic immunity is critical to the process of tumor rejection, cancer research has largely focused on immune cells in microenvironment. To understand molecular changes patient response (SR) presence BC, we profiled RNA blood and matched from 173 patients. We designed a system (MIxT, Matched Interactions Across Tissues) systematically explore link processes expressed each tissue. MIxT confirmed that active SR are especially relevant BC immunogenicity. The nature interactions across...

10.1371/journal.pcbi.1005680 article EN cc-by PLoS Computational Biology 2017-09-28

Tumor-host interactions extend beyond the local microenvironment and cancer development largely depends on ability of malignant cells to hijack exploit normal physiological processes host. Here, we established that many genes within peripheral blood show differential expression when an untreated breast (BC) is present, harnessed this fact construct a 50-gene signature distinguish BC patients from population-based controls. Our results were derived series large datasets our unique Norwegian...

10.1002/ijc.29030 article EN cc-by-nc International Journal of Cancer 2014-06-16

Chemotherapeutic agents such as anthracyclines and taxanes are commonly used in the neoadjuvant setting. Bevacizumab is an antibody which binds to vascular endothelial growth factor A (VEGFA) inhibits its receptor interaction, thus obstructing formation of new blood vessels. phase II randomized clinical trial 123 patients with Her2-negative breast cancer was conducted, treated chemotherapy (fluorouracil (5FU)/epirubicin/cyclophosphamide (FEC) taxane), or without bevacizumab. Serial biopsies...

10.1186/s13073-018-0601-y article EN cc-by Genome Medicine 2018-11-29
Hanla A. Park Sonja Neumeyer Kyriaki Michailidou Manjeet K. Bolla Qin Wang and 95 more Joe Dennis Thomas U. Ahearn Irene L. Andrulis Hoda Anton‐Culver Natalia Antonenkova Volker Arndt Kristan J. Aronson Annelie Augustinsson Adinda Baten Laura E. Beane Freeman Heiko Becher Matthias W. Beckmann Sabine Behrens Javier Benı́tez Marina Bermisheva Natalia Bogdanova Stig E. Bojesen Hiltrud Brauch Hermann Brenner Sara Y. Brucker Barbara Burwinkel Daniele Campa Federico Canzian Jose E. Castelao Stephen J. Chanock Georgia Chenevix‐Trench Christine L. Clarke Anne‐Lise Børresen‐Dale Grethe I.G. Alnæs Kristine Kleivi Sahlberg Lars Ottestad Rolf Kåresen Ellen Schlichting Marit Muri Holmen Toril Sauer Vilde Drageset Haakensen Olav Engebråten Bjørn Naume Alexander Fosså Cecile E. Kiserud Kristin V. Reinertsen Åslaug Helland Margit Riis Jürgen Geisler Don Conroy Fergus J. Couch Angela Cox Simon S. Cross Kamila Czene Mary B. Daly Peter Devilee Thilo Dörk Isabel dos‐Santos‐Silva Miriam Dwek Diana Eccles A. Heather Eliassen Christoph Engel Mikael Eriksson D. Gareth Evans Peter A. Fasching Henrik Flyger Lin Fritschi Montserrat García‐Closas José Á. García-Sáenz Mia M. Gaudet Graham G. Giles Gord Glendon Mark S. Goldberg David E. Goldgar Anna González‐Neira Mervi Grip Pascal Guénel Eric Hahnen Christopher A. Haiman Niclas Håkansson Per Hall Ute Hamann Sileny Han Elaine F. Harkness Steven N. Hart Wei He Bernadette A. M. Heemskerk‐Gerritsen John L. Hopper David J. Hunter Christine L. Clarke Deborah J. Marsh Rodney J. Scott Robert C. Baxter Desmond Yip Jane Carpenter Alison Davis Nirmala Pathmanathan Peter T. Simpson J. Dinny Graham Mythily Sachchithananthan

Abstract Background Despite a modest association between tobacco smoking and breast cancer risk reported by recent epidemiological studies, it is still equivocal whether causally related to risk. Methods We applied Mendelian randomisation (MR) evaluate potential causal effect of cigarette on Both individual-level data as well summary statistics for 164 single-nucleotide polymorphisms (SNPs) in genome-wide studies lifetime index (LSI) or per day (CPD) were used obtain MR estimates. Data from...

10.1038/s41416-021-01432-8 article EN cc-by British Journal of Cancer 2021-08-02
Anna Morra Maria Escala-Garcia Jonathan Beesley Renske Keeman Sander Canisius and 95 more Thomas U. Ahearn Irene L. Andrulis Hoda Anton‐Culver Volker Arndt Paul L. Auer Annelie Augustinsson Laura E. Beane Freeman Heiko Becher Matthias W. Beckmann Sabine Behrens Stig E. Bojesen Manjeet K. Bolla Hermann Brenner Thomas Brüning Saundra S. Buys Bette J. Caan Daniele Campa Federico Canzian Jose E. Castelao Jenny Chang‐Claude Stephen J. Chanock Ting‐Yuan David Cheng Christine L. Clarke Anne‐Lise Børresen‐Dale Kristine Kleivi Sahlberg Lars Ottestad Rolf Kåresen Ellen Schlichting Marit Muri Holmen Toril Sauer Vilde Drageset Haakensen Olav Engebråten Bjørn Naume Alexander Fosså Cecile E. Kiserud Kristin V. Reinertsen Åslaug Helland Margit Riis Jürgen Geisler Grethe I.G. Alnæs Sarah V. Colonna Fergus J. Couch Angela Cox Simon S. Cross Kamila Czene Mary B. Daly Joe Dennis Thilo Dörk Laure Dossus Alison M. Dunning Miriam Dwek Diana Eccles Arif B. Ekici A. Heather Eliassen Mikael Eriksson D. Gareth Evans Peter A. Fasching Henrik Flyger Lin Fritschi Manuela Gago‐Dominguez José Á. García-Sáenz Graham G. Giles Mervi Grip Pascal Guénel Melanie Gündert Eric Hahnen Christopher A. Haiman Niclas Håkansson Per Hall Ute Hamann Steven N. Hart Jaana M. Hartikainen Arndt Hartmann Wei He Maartje J. Hooning Reiner Hoppe John L. Hopper Anthony Howell David J. Hunter Christine L. Clarke Deborah J. Marsh Rodney J. Scott Robert Baxter Desmond Yip Jane Carpenter Alison Davis Nirmala Pathmanathan Peter T. Simpson J. Dinny Graham Mythily Sachchithananthan Agnes Jager Anna Jakubowska Wolfgang Janni Esther M. John Audrey Jung

Abstract Background Given the high heterogeneity among breast tumors, associations between common germline genetic variants and survival that may exist within specific subgroups could go undetected in an unstratified set of cancer patients. Methods We performed genome-wide association analyses 15 patients based on prognostic factors, including hormone receptors, tumor grade, age, type systemic treatment. Analyses were 91,686 female European ancestry from Breast Cancer Association Consortium,...

10.1186/s13058-021-01450-7 article EN cc-by Breast Cancer Research 2021-08-18

We report prospectively observed risk for breast cancer in kindreds without a demonstrable BRCA1/2 mutation. According to family history, the optimal available member(s) of each kindred attending our clinic was tested BRCA mutations. Women families mutation were subjected annual mammography. mutations demonstrated 496/2,118 (23 %) kindreds. In mutation, total 3,161 healthy women aged 25-59 years followed 24,808 observation years. Sixty-four cancers observed, compared 34.0 expected (p <...

10.1007/s10549-014-2902-1 article EN cc-by-nc Breast Cancer Research and Treatment 2014-03-11

Abstract BACKGROUND: In this phase II clinical trial, patients with HER2 negative primary tumors of ≥25 mm were treated neoadjuvant chemotherapy (4 x FEC100 + 12 weeks taxane-based therapy) and randomized (1:1) to receive bevacizumab or no bevacizumab. Mammography, ultrasound MR imaging used for response evaluation, in addition final pathology assessment. HYPOTHESIS: RPPA proteomic analyses support identification molecular mechanisms associated treatment. METHODS: Tumor responses evaluable...

10.1158/1538-7445.am2016-3268 article EN Cancer Research 2016-07-15
Jingjing Liu Ivona Lončar J. Margriet Collée Manjeet K. Bolla Joe Dennis and 95 more Kyriaki Michailidou Sophia Wang Irene L. Andrulis Monica Barile Matthias W. Beckmann Sabine Behrens Javier Benı́tez Carl Blomqvist Bram Boeckx Natalia Bogdanova Stig E. Bojesen Hiltrud Brauch Paul Brennan Hermann Brenner Annegien Broeks Barbara Burwinkel Jenny Chang‐Claude Shou‐Tung Chen Georgia Chenevix‐Trench Ching‐Yu Cheng Ji‐Yeob Choi Fergus J. Couch Angela Cox Simon S. Cross Katarina Ćuk Kamila Czene Thilo Dörk Isabel dos‐Santos‐Silva Peter A. Fasching Jonine D. Figueroa Henrik Flyger Montserrat García‐Closas Graham G. Giles Gord Glendon Mark S. Goldberg Anna González‐Neira Pascal Guénel Christopher A. Haiman Ute Hamann Steven N. Hart Mikael Hartman Sigrid Hatse John L. Hopper Hidemi Ito Anna Jakubowska Maria Kabisch Daehee Kang Veli‐Matti Kosma Vessela N. Kristensen Loı̈c Le Marchand Eunjung Lee Jingmei Li Artitaya Lophatananon Jan Lubiński Graham J. Mann Keitaro Matsuo Roger L. Milne Kristine Kleivi Sahlberg Lars Ottestad Rolf Kåresen Anita Langerød Ellen Schlichting Marit Muri Holmen Toril Sauer Vilde Drageset Haakensen Olav Engebråten Bjørn Naume Cecile E. Kiserud Kristin V. Reinertsen Åslaug Helland Margit Riis Ida Bukholm Per Eystein Lønning Anne‐Lise Børresen‐Dale Grethe I.G. Alnæs Susan L. Neuhausen Heli Nevanlinna Nick Orr José Ignacio Arias Pérez Julian Peto Thomas Choudary Putti Katri Pylkäs Paolo Radice Suleeporn Sangrajrang Elinor J. Sawyer Marjanka K. Schmidt Andreas Schneeweiß Chen‐Yang Shen Martha J. Shrubsole Xiao‐Ou Shu Jacques Simard Melissa C. Southey Anthony J. Swerdlow Soo‐Hwang Teo Daniel C. Tessier

Abstract NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs2735383 G &gt; C, located a microRNA binding site the 3′-untranslated region (UTR) of NBS1 , was shown to be associated with increased susceptibility lung and colorectal cancer. However, relation between breast cancer is not yet clear. Therefore, we genotyped 1,170 familial non- BRCA1/2 cases 1,077 controls using PCR-based restriction fragment length polymorphism (RFLP-PCR) analysis,...

10.1038/srep36874 article EN cc-by Scientific Reports 2016-11-15
Jingjing Liu Wendy J.C. Prager ‐ van der Smissen J. Margriet Collée Manjeet K. Bolla Qin Wang and 95 more Kyriaki Michailidou Joe Dennis Thomas U. Ahearn Kristiina Aittomäki Christine B. Ambrosone Irene L. Andrulis Hoda Anton‐Culver Natalia Antonenkova Volker Arndt Norbert Arnold Kristan J. Aronson Annelie Augustinsson Päivi Auvinen Heiko Becher Matthias W. Beckmann Sabine Behrens Marina Bermisheva Leslie Bernstein Natalia Bogdanova Nadja Bogdanova-Markov Stig E. Bojesen Hiltrud Brauch Hermann Brenner Ignacio Briceño Sara Y. Brucker Thomas Brüning Barbara Burwinkel Qiuyin Cai Hui Cai Daniele Campa Federico Canzian Jose E. Castelao Jenny Chang‐Claude Stephen J. Chanock Ji‐Yeob Choi Melissa Christiaens Christine L. Clarke Kristine Kleivi Sahlberg Anne‐Lise Børresen‐Dale Lars Ottestad Rolf Kåresen Ellen Schlichting Marit Muri Holmen Toril Sauer Vilde Drageset Haakensen Olav Engebråten Bjørn Naume Alexander Fosså Cecile E. Kiserud Kristin V. Reinertsen Åslaug Helland Margit Riis Jürgen Geisler Tone F. Bathen Elin Borgen Britt Fritzman Øystein Garred Gry Aarum Geitvik Solveig Hofvind Anita Langerød Ole Christian Lingjærde Gunhild M. Mælandsmo Hege G. Russnes Helle Kristine Skjerven Thérese Sørlie Grethe I.G. Alnæs Fergus J. Couch Kamila Czene Mary B. Daly Peter Devilee Isabel dos‐Santos‐Silva Miriam Dwek Diana Eccles A. Heather Eliassen Peter A. Fasching Jonine D. Figueroa Henrik Flyger Lin Fritschi Manuela Gago‐Dominguez Susan M. Gapstur Montserrat García‐Closas José Á. García-Sáenz Mia M. Gaudet Graham G. Giles Mark S. Goldberg David E. Goldgar Pascal Guénel Christopher A. Haiman Niclas Håkansson Per Hall Patricia Harrington Steven N. Hart Mikael Hartman Peter Hillemanns John L. Hopper

Abstract In breast cancer, high levels of homeobox protein Hox-B13 (HOXB13) have been associated with disease progression ER-positive cancer patients and resistance to tamoxifen treatment. Since HOXB13 p.G84E is a prostate risk allele, we evaluated the association between germline mutations in previous study consisting 3,270 familial non- BRCA1/2 cases 2,327 controls from Netherlands. Although both recurrent p.R217C were not risk, estimation for was very precise. To provide more conclusive...

10.1038/s41598-020-65665-y article EN cc-by Scientific Reports 2020-06-16

High mammographic density (MD) is associated with a 4–6 times increase in breast cancer risk. For post-menopausal women, MD often decreases over time, but little known about the underlying biological mechanisms. reflects tissue composition, and may be microenvironment subtypes previously identified tumor-adjacent normal tissue. Currently, these have not been explored We obtained biopsies from breasts of healthy women at two different time points several years apart performed microarray gene...

10.1007/s10911-018-09423-x article EN cc-by Journal of Mammary Gland Biology and Neoplasia 2019-01-06

Abstract The NeoAva study is a phase II clinical trial of patients with HER2 negative primary tumors ≥25 mm treated neoadjuvant chemotherapy (4 x FEC100 + 12 weeks taxane-based therapy) and randomized (1:1) to receive bevacizumab or no bevacizumab. Mammography, ultrasound MR imaging were used for response evaluation, in addition final pathology assessment. Tumor evaluable 131 patients; which 66 received chemotherapy. material was obtained at screening, into treatment surgical removal 25...

10.1158/1538-7445.sabcs14-p4-11-14 article EN Cancer Research 2015-05-01

2523 Background: The molecular characteristics of responding and non-responding breast cancers when treated with antiangiogenic therapy are largely unknown. Methods: To investigate alterations in tumors therapy, the NeoAva study included patients HER2 negative primary ≥ 25 mm that were randomized (1:1) to receive chemotherapy (4 x FEC100 + 12 weeks taxane-based therapy) or without bevacizumab. Tumor material was obtained at screening, into treatment surgical removal weeks. mRNA expression...

10.1200/jco.2015.33.15_suppl.2523 article EN Journal of Clinical Oncology 2015-05-20

Mammographic features of calcifications on mammograms showing invasive breast cancer are associated with survival. Less is known about mammographic and progression to among women treated for ductal carcinoma in situ (DCIS).To investigate screen-detected DCIS who later did not get diagnosed cancer.This registry-based nested case-control study analyzed data from BreastScreen Norway, 1995-2016. Within this cohort DCIS, those were (cases) matched (1:2) (controls) after their by the end 2016....

10.1177/02841851211006319 article EN Acta Radiologica 2021-04-22
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