Charles M. Perou

ORCID: 0000-0001-9827-2247
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About
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Research Areas
  • Cancer Genomics and Diagnostics
  • Breast Cancer Treatment Studies
  • Cancer Cells and Metastasis
  • HER2/EGFR in Cancer Research
  • Cancer Immunotherapy and Biomarkers
  • Gene expression and cancer classification
  • Advanced Breast Cancer Therapies
  • RNA modifications and cancer
  • Estrogen and related hormone effects
  • Lung Cancer Treatments and Mutations
  • Cancer-related Molecular Pathways
  • Molecular Biology Techniques and Applications
  • Cancer Treatment and Pharmacology
  • BRCA gene mutations in cancer
  • Single-cell and spatial transcriptomics
  • Bioinformatics and Genomic Networks
  • Radiomics and Machine Learning in Medical Imaging
  • Cancer-related molecular mechanisms research
  • Epigenetics and DNA Methylation
  • Ferroptosis and cancer prognosis
  • Computational Drug Discovery Methods
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer, Hypoxia, and Metabolism
  • Advanced Biosensing Techniques and Applications
  • RNA Research and Splicing

University of North Carolina at Chapel Hill
2016-2025

UNC Lineberger Comprehensive Cancer Center
2016-2025

European University Cyprus
2025

Segeberger Kliniken
2011-2024

ARUP Institute for Clinical and Experimental Pathology
2009-2023

University of North Carolina Health Care
2007-2023

The University of Texas Health Science Center at Houston
2023

Mayo Clinic in Florida
2015-2022

Pediatrics and Genetics
2010-2022

Queen's University Belfast
2019

Daniel C. Koboldt Robert S. Fulton Michael D. McLellan Heather K. Schmidt Joelle Kalicki-Veizer and 95 more Joshua F. McMichael Lucinda Fulton David J. Dooling Li Ding Elaine R. Mardis Richard K. Wilson Adrian Ally Miruna Balasundaram Yaron S.N. Butterfield Rebecca Carlsen Candace Carter Andy Chu Eric Chuah Hye Jung E. Chun Robin Coope Noreen Dhalla Ranabir Guin Carrie Hirst Martin Hirst Robert A. Holt Darlene Lee Haiyan I. Li Michael Mayo Richard A. Moore Andrew J. Mungall Erin Pleasance A. Gordon Robertson Jacqueline E. Schein Arash Shafiei Payal Sipahimalani Jared R. Slobodan Dominik Stoll Angela Tam Nina Thiessen Richard Varhol Natasja Wye Thomas Zeng Yongjun Zhao İnanç Birol Steven J.M. Jones Marco A. Marra Andrew D. Cherniack Gordon Saksena Robert C. Onofrio Nam Pho Scott L. Carter Steven E. Schumacher Barbara Tabak Bryan Hernandez Jeff Gentry Huy Nguyen Andrew Crenshaw Kristin Ardlie Rameen Beroukhim Wendy Winckler Gad Getz Stacey Gabriel Matthew Meyerson Lynda Chin Raju Kucherlapati Katherine A. Hoadley J. Todd Auman Huihui Fan Yidi J. Turman Yan Shi Ling Li Michael D. Topal Xiaping He Hann Hsiang Chao Aleix Prat Grace O. Silva Michael D. Iglesia Zhao Wei Jerry Usary Jonathan S. Berg Michael C. C. Adams Jessica K. Booker Junyuan Wu Anisha Gulabani Tom Bodenheimer Alan P. Hoyle Janae V. Simons Matthew G. Soloway Lisle E. Mose Joshua M. Stuart Saianand Balu Peter J. Park D. Neil Hayes Charles M. Perou Simeen Malik Swapna Mahurkar‐Joshi Hui Shen Daniel J. Weisenberger Timothy J. Triche Phillip H. Lai

We analysed primary breast cancers by genomic DNA copy number arrays, methylation, exome sequencing, messenger RNA microRNA sequencing and reverse-phase protein arrays. Our ability to integrate information across platforms provided key insights into previously defined gene expression subtypes demonstrated the existence of four main cancer classes when combining data from five platforms, each which shows significant molecular heterogeneity. Somatic mutations in only three genes (TP53, PIK3CA...

10.1038/nature11412 article EN cc-by-nc-sa Nature 2012-09-21

The purpose of this study was to classify breast carcinomas based on variations in gene expression patterns derived from cDNA microarrays and correlate tumor characteristics clinical outcome. A total 85 microarray experiments representing 78 cancers, three fibroadenomas, four normal tissues were analyzed by hierarchical clustering. As reported previously, the cancers could be classified into a basal epithelial-like group, an ERBB2 -overexpressing group breast-like expression. novel finding...

10.1073/pnas.191367098 article EN Proceedings of the National Academy of Sciences 2001-09-11

Characteristic patterns of gene expression measured by DNA microarrays have been used to classify tumors into clinically relevant subgroups. In this study, we refined the previously defined subtypes breast that could be distinguished their distinct expression. A total 115 malignant were analyzed hierarchical clustering based on 534 "intrinsic" genes and shown subdivide one basal-like, ERBB2-overexpressing, two luminal-like, normal tissue-like subgroup. The for classification selected similar...

10.1073/pnas.0932692100 article EN Proceedings of the National Academy of Sciences 2003-06-26
Gad Getz Stacey B. Gabriel Kristian Cibulskis Eric Lander Andrey Sivachenko and 95 more Carrie Sougnez Robert Lawrence Cyriac Kandoth David J. Dooling Robert W. Fulton Lucinda Fulton Joelle Kalicki-Veizer Michael D. McLellan Michelle D. O’Laughlin Heather K. Schmidt Richard K. Wilson Kai Ye Li Ding Adrian Ally Miruna Balasundaram İnanç Birol Yaron S.N. Butterfield Rebecca Carlsen Candace Carter Andy Chu Eric Chuah Hye Jung E. Chun Noreen Dhalla Ranabir Guin Carrie Hirst Robert A. Holt Steven J.M. Jones Darlene Lee Haiyan I. Li Marco A. Marra Michael Mayo Richard A. Moore Andrew J. Mungall Patrick Plettner Jacqueline E. Schein Payal Sipahimalani Angela Tam Richard Varhol A. Gordon Robertson Andrew D. Cherniack Itai Pashtan Gordon Saksena Robert C. Onofrio Steven E. Schumacher Barbara Tabak Scott L. Carter Bryan Hernandez Jeff Gentry Helga B. Salvesen Kristin Ardlie Wendy Winckler Rameen Beroukhim Matthew Meyerson Angela Hadjipanayis Semin Lee Harshad S. Mahadeshwar Peter J. Park Alexei Protopopov Xiaojia Ren Sahil Seth Xingzhi Song Jiabin Tang Ruibin Xi Lixing Yang Zeng Dong Raju Kucherlapati Lynda Chin Jianhua Zhang J. Todd Auman Saianand Balu Tom Bodenheimer Elizabeth Buda D. Neil Hayes Alan P. Hoyle Joshua M. Stuart Corbin D. Jones Shaowu Meng Piotr A. Mieczkowski Lisle E. Mose Joel S. Parker Charles M. Perou Jeffrey Roach Yan Shi Janae V. Simons Mathew G. Soloway Donghui Tan Michael D. Topal Stephen C. Waring Junyuan Wu Katherine A. Hoadley Stephen B. Baylin Moiz Bootwalla Phillip H. Lai Timothy J. Triche David Van Den Berg

We performed an integrated genomic, transcriptomic and proteomic characterization of 373 endometrial carcinomas using array- sequencing-based technologies. Uterine serous tumours ∼25% high-grade endometrioid had extensive copy number alterations, few DNA methylation changes, low oestrogen receptor/progesterone receptor levels, frequent TP53 mutations. Most alterations or mutations, but mutations in PTEN, CTNNB1, PIK3CA, ARID1A KRAS novel the SWI/SNF chromatin remodelling complex gene ARID5B....

10.1038/nature12113 article EN cc-by-nc-sa Nature 2013-04-30
Cameron Brennan Roel G.W. Verhaak Aaron McKenna Benito Campos Houtan Noushmehr and 95 more Sofie R. Salama Siyuan Zheng Debyani Chakravarty Zack Sanborn Samuel H. Berman Rameen Beroukhim Brady Bernard Chang‐Jiun Wu Giannicola Genovese Ilya Shmulevich Jill S. Barnholtz‐Sloan Lihua Zou Rahulsimham Vegesna Sachet A. Shukla Giovanni Ciriello W. K. Alfred Yung Wei Zhang Carrie Sougnez Tom Mikkelsen Kenneth Aldape Darell D. Bigner Erwin G. Van Meir Michael D. Prados Andrew E. Sloan Keith L. Black Jennifer Eschbacher Gaetano Finocchiaro William A. Friedman David W. Andrews Abhijit Guha Mary Iacocca Brian Patrick O’Neill Greg Foltz Jerome Myers Daniel J. Weisenberger Robert Penny Raju Kucherlapati Charles M. Perou D. Neil Hayes Richard A. Gibbs Marco A. Marra Gordon B. Mills Eric S. Lander Paul T. Spellman Richard K. Wilson Chris Sander John N. Weinstein Matthew Meyerson Stacey Gabriel Peter W. Laird David Haussler Gad Getz Lynda Chin Christopher C. Benz Jill S. Barnholtz‐Sloan Wendi Barrett Quinn T. Ostrom Yingli Wolinsky Keith L. Black Bikash Bose Paul T. Boulos Madgy Boulos Jenn Brown Christine Czerinski Matthew Eppley Mary Iacocca Thelma Kempista Teresa Kitko Yakov Koyfman Brenda Rabeno Pawan Rastogi Michael C. Sugarman Patricia Swanson Kennedy Yalamanchii Ilana P. Otey Yingchun Spring Liu Yonghong Xiao J. Todd Auman Peng‐Chieh Chen Angela Hadjipanayis Eunjung Lee Semin Lee Peter J. Park Jonathan G. Seidman Lixing Yang Raju Kucherlapati Steven N. Kalkanis Tom Mikkelsen Laila Poisson Aditya Raghunathan Lisa Scarpace Brady Bernard Ryan Bressler Andrea Eakin Lisa Iype

10.1016/j.cell.2013.09.034 article EN publisher-specific-oa Cell 2013-10-01

Purpose To improve on current standards for breast cancer prognosis and prediction of chemotherapy benefit by developing a risk model that incorporates the gene expression–based “intrinsic” subtypes luminal A, B, HER2-enriched, basal-like. Methods A 50-gene subtype predictor was developed using microarray quantitative reverse transcriptase polymerase chain reaction data from 189 prototype samples. Test sets 761 patients (no systemic therapy) were evaluated prognosis, 133 pathologic complete...

10.1200/jco.2008.18.1370 article EN public-domain Journal of Clinical Oncology 2009-02-10

A HETEROGeneous disease composed of a growing number recognized biological subtypes.The prognostic and etiologic importance this diversity is complicated by many factors, including the observation that differences in clinical outcomes often correlate with race.Age-adjusted mortality United States from breast cancer white women 28.3 deaths per 100 000 compared 36.4 African American women. 1 This disparity particularly pronounced among younger than 50 years, whom 77% higher (11.0 vs 6.3...

10.1001/jama.295.21.2492 article EN JAMA 2006-06-06
Michael S. Lawrence Carrie Sougnez Lee Lichtenstein Kristian Cibulskis Eric S. Lander and 95 more Stacey Gabriel Gad Getz Adrian Ally Miruna Balasundaram İnanç Birol Reanne Bowlby Denise Brooks Yaron S.N. Butterfield Rebecca Carlsen Dean Cheng Andy Chu Noreen Dhalla Ranabir Guin Robert A. Holt Steven J.M. Jones Darlene Lee Haiyan I. Li Marco A. Marra Michael Mayo Richard A. Moore Andrew J. Mungall A. Gordon Robertson Jacqueline E. Schein Payal Sipahimalani Angela Tam Nina Thiessen Tina Wong Alexei Protopopov Netty Santoso Semin Lee Michael Parfenov Jianhua Zhang Harshad S. Mahadeshwar Jiabin Tang Xiaojia Ren Sahil Seth Psalm Haseley Dong Zeng Lixing Yang Andrew Wei Xu Xingzhi Song Angeliki Pantazi Christopher A. Bristow Angela Hadjipanayis Jonathan G. Seidman Lynda Chin Peter J. Park Raju Kucherlapati Rehan Akbani Tod D. Casasent Wenbin Liu Yiling Lu Gordon B. Mills Thomas Motter John N. Weinstein Lixia Diao Jing Wang You Hong Fan Jinze Liu Kai Wang J. Todd Auman Saianand Balu Thomas Bodenheimer Elizabeth Buda D. Neil Hayes Katherine A. Hoadley Alan P. Hoyle Joshua M. Stuart Corbin D. Jones Patrick K. Kimes Yufeng Liu J. S. Marron Shaowu Meng Piotr A. Mieczkowski Lisle E. Mose Joel S. Parker Charles M. Perou Jan F. Prins Jeffrey Roach Yan Shi Janae V. Simons Darshan Singh Matthew G. Soloway Donghui Tan Umadevi Veluvolu Vonn Walter Stephen C. Waring Matthew D. Wilkerson Junyuan Wu Ni Zhao Andrew D. Cherniack Peter S. Hammerman Aaron D. Tward Chandra Sekhar Pedamallu Gordon Saksena

The Cancer Genome Atlas profiled 279 head and neck squamous cell carcinomas (HNSCCs) to provide a comprehensive landscape of somatic genomic alterations. Here we show that human-papillomavirus-associated tumours are dominated by helical domain mutations the oncogene PIK3CA, novel alterations involving loss TRAF3, amplification cycle gene E2F1. Smoking-related HNSCCs demonstrate near universal loss-of-function TP53 CDKN2A inactivation with frequent copy number including 3q26/28 11q13/22. A...

10.1038/nature14129 article EN cc-by-nc-sa Nature 2015-01-27

The 13th St Gallen International Breast Cancer Conference (2013) Expert Panel reviewed and endorsed substantial new evidence on aspects of the local regional therapies for early breast cancer, supporting less extensive surgery to axilla shorter durations radiation therapy. It refined its earlier approach classification management luminal disease in absence amplification or overexpression Human Epidermal growth factor Receptor 2 (HER2) oncogene, while retaining essentially unchanged...

10.1093/annonc/mdt303 article EN cc-by-nc Annals of Oncology 2013-08-06

Abstract Purpose: Expression profiling studies classified breast carcinomas into estrogen receptor (ER)+/luminal, normal breast-like, HER2 overexpressing, and basal-like groups, with the latter two associated poor outcomes. Currently, there exist clinical assays that identify ER+/luminal HER2-overexpressing tumors, we sought to develop a assay for tumors. Experimental Design: To an immunohistochemical profile collected series of known tumors tested them protein patterns are characteristic...

10.1158/1078-0432.ccr-04-0220 article EN Clinical Cancer Research 2004-08-15

Gene expression profiling of breast cancer has identified two biologically distinct estrogen receptor (ER)-positive subtypes cancer: luminal A and B. Luminal B tumors have higher proliferation poorer prognosis than tumors. In this study, we developed a clinically practical immunohistochemistry assay to distinguish from investigated its ability separate according recurrence-free disease-specific survival. Tumors cohort 357 patients with invasive carcinomas were subtyped by gene profile....

10.1093/jnci/djp082 article EN cc-by-nc JNCI Journal of the National Cancer Institute 2009-05-13

Abstract Introduction In breast cancer, gene expression analyses have defined five tumor subtypes (luminal A, luminal B, HER2-enriched, basal-like and claudin-low), each of which has unique biologic prognostic features. Here, we comprehensively characterize the recently identified claudin-low subtype. Methods The clinical, pathological biological features tumors were compared to other using an updated human database multiple independent data sets. These main also evaluated in a panel cancer...

10.1186/bcr2635 article EN cc-by Breast Cancer Research 2010-09-02

Abstract Purpose: Gene expression analysis identifies several breast cancer subtypes. We examined the relationship of neoadjuvant chemotherapy response to outcome among these Experimental Design: used immunohistochemical profiles [human epidermal growth factor receptor 2–positive (HER2+)/hormone receptor–negative for HER2+/estrogen (ER−), hormone and HER2− basal-like, receptor–positive luminal] subtype a prospectively maintained data set patients with treated anthracycline-based (doxorubicin...

10.1158/1078-0432.ccr-06-1109 article EN Clinical Cancer Research 2007-04-15

Abstract Purpose: Molecular classification of breast cancer has been proposed based on gene expression profiles human tumors. Luminal, basal-like, normal-like, and erbB2+ subgroups were identified shown to have different prognoses. The goal this research was determine if these molecular subtypes also respond differently preoperative chemotherapy. Experimental Design: Fine needle aspirations 82 cancers obtained before starting paclitaxel followed by 5-fluorouracil, doxorubicin,...

10.1158/1078-0432.ccr-04-2421 article EN Clinical Cancer Research 2005-08-15
Giovanni Ciriello Michael L. Gatza Andrew H. Beck Matthew D. Wilkerson Suhn K. Rhie and 95 more Alessandro Pastore Hailei Zhang Michael D. McLellan Christina Yau Cyriac Kandoth Reanne Bowlby Hui Shen Sikander Hayat Robert J. Fieldhouse Susan C. Lester Gary M. Tse Rachel E. Factor Laura C. Collins Kimberly H. Allison Yunn-Yi Chen Kristin C. Jensen Nicole B. Johnson Steffi Oesterreich Gordon B. Mills Andrew D. Cherniack Gordon Robertson Christopher C. Benz Chris Sander Peter W. Laird Katherine A. Hoadley Tari A. King Charles M. Perou Rehan Akbani J. Todd Auman Miruna Balasundaram Saianand Balu Thomas Barr Andrew H. Beck Christopher C. Benz Stephen C. Benz Mario Berríos Rameen Beroukhim Tom Bodenheimer Lori Boice Arnoud Boot Jay Bowen Reanne Bowlby Denise Brooks Andrew D. Cherniack Lynda Chin Juok Cho Sudha Chudamani Giovanni Ciriello Tanja M. Davidsen John A. Demchok Jennifer B. Dennison Li Ding Ina Felau Martin L. Ferguson Scott Frazer Stacey Gabriel Jianjiong Gao Julie M. Gastier-Foster Michael L. Gatza Nils Gehlenborg Mark Gerken Gad Getz William J. Gibson D. Neil Hayes David I. Heiman Katherine A. Hoadley Andrea Holbrook Robert A. Holt Alan P. Hoyle Hai Hu Mei Huang Carolyn M. Hutter E. Shelley Hwang Joshua M. Stuart Steven J.M. Jones Zhenlin Ju Jaegil Kim Phillip H. Lai Peter W. Laird Michael S. Lawrence Kristen M. Leraas Tara M. Lichtenberg Pei Lin Shiyun Ling Jia Liu Wenbin Liu Laxmi Lolla Yiling Lu Yussanne Ma Dennis T. Maglinte Elaine R. Mardis Jeffrey R. Marks Marco A. Marra Cynthia McAllister Michael D. McLellan

10.1016/j.cell.2015.09.033 article EN publisher-specific-oa Cell 2015-10-01

The genome-wide program of gene expression during the cell division cycle in a human cancer line (HeLa) was characterized using cDNA microarrays. Transcripts >850 genes showed periodic variation cycle. Hierarchical clustering patterns revealed coexpressed groups previously well-characterized involved essential processes such as DNA replication, chromosome segregation, and adhesion along with uncharacterized function. Most whose had been reported to correlate proliferative state tumors...

10.1091/mbc.02-02-0030 article EN Molecular Biology of the Cell 2002-06-01

cDNA microarrays and a clustering algorithm were used to identify patterns of gene expression in human mammary epithelial cells growing culture primary breast tumors. Clusters coexpressed genes identified through manipulations vitro also showed consistent variation among tumor samples. By using immunohistochemistry with antibodies against proteins encoded by particular cluster, the identity cell type within specimen that contributed observed pattern could be determined. coherent cultured...

10.1073/pnas.96.16.9212 article EN Proceedings of the National Academy of Sciences 1999-08-03
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