A. Ari Hakimi

ORCID: 0000-0002-0930-8824
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About
Contact & Profiles
Research Areas
  • Renal cell carcinoma treatment
  • Renal and related cancers
  • Cancer Genomics and Diagnostics
  • Bladder and Urothelial Cancer Treatments
  • Ferroptosis and cancer prognosis
  • Cancer Immunotherapy and Biomarkers
  • Multiple and Secondary Primary Cancers
  • Epigenetics and DNA Methylation
  • Urinary and Genital Oncology Studies
  • Cancer, Hypoxia, and Metabolism
  • Prostate Cancer Diagnosis and Treatment
  • Pancreatic and Hepatic Oncology Research
  • Radiomics and Machine Learning in Medical Imaging
  • Pediatric Urology and Nephrology Studies
  • Renal and Vascular Pathologies
  • Cancer, Lipids, and Metabolism
  • Immune cells in cancer
  • Cancer Diagnosis and Treatment
  • Urologic and reproductive health conditions
  • Genetic and Kidney Cyst Diseases
  • Metabolomics and Mass Spectrometry Studies
  • CNS Lymphoma Diagnosis and Treatment
  • Genetic factors in colorectal cancer
  • Lung Cancer Treatments and Mutations
  • Immune Cell Function and Interaction

Memorial Sloan Kettering Cancer Center
2016-2025

Ministry Of Health
2025

Kettering University
2015-2023

Pacific Northwest National Laboratory
2022

Hefei Institutes of Physical Science
2022

Chinese Academy of Sciences
2022

Cornell University
2013-2020

New York Proton Center
2012-2019

Kettering Medical Center
2019

Massachusetts General Hospital
2018

Ahmet Zehir Ryma Benayed Ronak Shah Aijazuddin Syed Sumit Middha and 95 more Hyunjae R. Kim Preethi Srinivasan Jianjiong Gao Debyani Chakravarty Sean M. Devlin Matthew D. Hellmann David Barron Alison M. Schram Meera Hameed Snjezana Doğan Dara S. Ross Jaclyn F. Hechtman Deborah F. DeLair JinJuan Yao Diana Mandelker Donavan T. Cheng Raghu Chandramohan Abhinita Mohanty Ryan Ptashkin Gowtham Jayakumaran Meera Prasad Mustafa Syed Anoop Balakrishnan Rema Zhen Y. Liu Khédoudja Nafa Laetitia Borsu Justyna Sadowska Jacklyn Casanova Ruben Bacares Iwona Kiecka Anna Razumova Julie B Son Lisa Stewart Tessara Baldi Kerry Mullaney Hikmat Al‐Ahmadie Efsevia Vakiani Adam Abeshouse Alexander Penson Philip Jonsson Niedzica Camacho Matthew T. Chang Helen Won Benjamin Groß Ritika Kundra Zachary Heins Hsiao‐Wei Chen Sarah Phillips Hongxin Zhang Jiaojiao Wang Angelica Ochoa Jonathan Wills Michael Eubank Stacy B. Thomas Stuart M. Gardos Dalicia N. Reales Jesse Galle Robert Durany Roy Cambria Wassim Abida Andrea Cercek Darren R. Feldman Mrinal M. Gounder A. Ari Hakimi James J. Harding Gopa Iyer Yelena Y. Janjigian Emmet Jordan Ciara M. Kelly Maeve A. Lowery Luc G.T. Morris Antonio Omuro Nitya Raj Pedram Razavi Alexander N. Shoushtari Neerav Shukla Tara E. Soumerai Anna M. Varghese Rona Yaeger Jonathan Coleman Bernard H. Bochner Gregory J. Riely Leonard B. Saltz Howard I. Scher Paul Sabbatini Mark E. Robson David S. Klimstra Barry S. Taylor José Baselga Nikolaus Schultz David M. Hyman Maria E. Arcila David B. Solit Marc Ladanyi Michael F. Berger

10.1038/nm.4333 article EN Nature Medicine 2017-05-08
W. Marston Linehan Paul T. Spellman Christopher J. Ricketts Chad J. Creighton Suzanne S. Fei and 95 more Caleb Davis David A. Wheeler Bradley A. Murray Laura S. Schmidt Cathy D. Vocke Myron Peto Abu Amar M. Al Mamun Eve Shinbrot Anurag Sethi Samira A. Brooks W. Kimryn Rathmell Angela N. Brooks Katherine A. Hoadley A. Gordon Robertson Denise Brooks Reanne Bowlby Sara Sadeghi Hui Shen Daniel J. Weisenberger Arnoud Boot Stephen B. Baylin Peter W. Laird Andrew D. Cherniack Gordon Saksena Scott M. Haake Jun Li Liang Han Yiling Lu Gordon B. Mills Rehan Akbani Mark D.M. Leiserson Benjamin J. Raphael Pavana Anur Donald P. Bottaro Laurence Albigès Nandita Barnabas Toni K. Choueiri Bogdan Czerniak Andrew K. Godwin A. Ari Hakimi Thai H. Ho James J. Hsieh Michael Ittmann William Y. Kim Bhavani Krishnan Maria J. Merino Kenna Shaw Victor E. Reuter Ed Reznik Carl Simon Shelley Hai Hu Sabina Signoretti Ramaprasad Srinivasan Pheroze Tamboli George Thomas Satish K. Tickoo Kenneth Burnett Daniel Crain Johanna Gardner Kevin Lau David Mallery Scott Morris Joseph Paulauskis Robert Penny Candace Shelton W. Troy Shelton Mark E. Sherman Eric Thompson Peggy Yena Melissa Avedon Jay Bowen Julie M. Gastier-Foster Mark Gerken Kristen M. Leraas Tara M. Lichtenberg Nilsa C. Ramirez Tracie Santos Lisa Wise Erik Zmuda John A. Demchok Ina Felau Carolyn M. Hutter Margi Sheth Heidi J. Sofia Roy Tarnuzzer Zhining Wang Liming Yang Jean C. Zenklusen Jiashan Zhang Brenda Ayala Julien Baboud Sudha Chudamani Jia Liu Laxmi Lolla Rashi Naresh

Papillary renal-cell carcinoma, which accounts for 15 to 20% of carcinomas, is a heterogeneous disease that consists various types renal cancer, including tumors with indolent, multifocal presentation and solitary an aggressive, highly lethal phenotype. Little known about the genetic basis sporadic papillary no effective forms therapy advanced exist.We performed comprehensive molecular characterization 161 primary using whole-exome sequencing, copy-number analysis, messenger RNA microRNA...

10.1056/nejmoa1505917 article EN New England Journal of Medicine 2015-11-04

Tumor-infiltrating immune cells have been linked to prognosis and response immunotherapy; however, the levels of distinct cell subsets signals that draw them into a tumor, such as expression antigen presenting machinery genes, remain poorly characterized. Here, we employ gene expression-based computational method profile infiltration 24 populations in 19 cancer types. We compare types using an score T find clear renal carcinoma (ccRCC) is among highest for both scores. Using profiles well...

10.1186/s13059-016-1092-z article EN cc-by Genome biology 2016-11-17

Recent clinical trials have demonstrated a clear survival advantage in advanced head and neck squamous cell carcinoma (HNSCC) patients treated with immune checkpoint blockade. These emerging results reveal that HNSCC is one of the most promising frontiers for immunotherapy research. However, further progress immuno-oncology will require detailed understanding infiltrative landscape found these tumors. We leveraged transcriptome data from 280 tumors profiled by The Cancer Genome Atlas (TCGA)...

10.1172/jci.insight.89829 article EN JCI Insight 2016-10-19

Renal cell carcinoma (RCC) is not a single disease, but several histologically defined cancers with different genetic drivers, clinical courses, and therapeutic responses. The current study evaluated 843 RCC from the three major histologic subtypes, including 488 clear RCC, 274 papillary 81 chromophobe RCC. Comprehensive genomic phenotypic analysis of subtypes reveals distinctive features each subtype that provide foundation for development subtype-specific management strategies patients...

10.1016/j.celrep.2018.03.075 article EN cc-by Cell Reports 2018-04-01
David Clark Saravana M. Dhanasekaran Francesca Petralia Jianbo Pan Xiaoyu Song and 95 more Yingwei Hu Felipe da Veiga Leprevost Boris Reva T. Mamie Lih Hui-Yin Chang Weiping Ma Chen Huang Christopher J. Ricketts Lijun Chen Azra Krek Yize Li Dmitry Rykunov Qing Kay Li Lin S. Chen Umut Özbek Suhas Vasaikar Yige Wu Seungyeul Yoo Shrabanti Chowdhury Matthew A. Wyczalkowski Jiayi Ji Michael Schnaubelt Andy T. Kong Sunantha Sethuraman Dmitry M. Avtonomov Minghui Ao Antonio Colaprico Song Cao Kyung-Cho Cho Selim Kalaycı Shiyong Ma Wenke Liu Kelly V. Ruggles Anna Calinawan Zeynep H. Gümüş Daniel Geiszler Emily Kawaler Guo Ci Teo Bo Wen Yuping Zhang Sarah Keegan Kai Li Feng Chen Nathan Edwards Phillip M. Pierorazio Xi Steven Chen Christian P. Pavlovich A. Ari Hakimi Gabriel Bromiński James J. Hsieh Andrzej Antczak Tatiana Omelchenko Jan Lubiński Maciej Wiznerowicz W. Marston Linehan Christopher R. Kinsinger Mathangi Thiagarajan Emily S. Boja Mehdi Mesri Tara Hiltke Ana I. Robles Henry Rodriguez Jiang Qian David Fenyö Bing Zhang Li Ding Eric E. Schadt Arul M. Chinnaiyan Zhen Zhang Gilbert S. Omenn Marcin Cieślik Daniel W. Chan Alexey I. Nesvizhskii Pei Wang Hui Zhang A. Samad Hashimi Alexander R. Pico Alla Karpova Alyssa Charamut Amanda G. Paulovich Amy M. Perou Anna Malovannaya Annette Marrero-Oliveras Anupriya Agarwal Barbara Hindenach Barbara L. Pruetz Beom‐Jun Kim Brian J. Druker Chelsea J. Newton Chet Birger Corbin D. Jones Cristina E. Tognon D.R. Mani Dana R. Valley Daniel C. Rohrer

To elucidate the deregulated functional modules that drive clear cell renal carcinoma (ccRCC), we performed comprehensive genomic, epigenomic, transcriptomic, proteomic, and phosphoproteomic characterization of treatment-naive ccRCC paired normal adjacent tissue samples. Genomic analyses identified a distinct molecular subgroup associated with genomic instability. Integration proteogenomic measurements uniquely protein dysregulation cellular mechanisms impacted by alterations, including...

10.1016/j.cell.2019.10.007 article EN cc-by Cell 2019-10-01

Mutations, deletions, and changes in copy number of mitochondrial DNA (mtDNA), are observed throughout cancers. Here, we survey mtDNA variation across 22 tumor types profiled by The Cancer Genome Atlas project. We observe a tendency for some cancers, especially the bladder, breast, kidney, to be depleted mtDNA, relative matched normal tissue. Analysis genetic context reveals an association between incidence several somatic alterations, including IDH1 mutations gliomas, content. In but not...

10.7554/elife.10769 article EN cc-by eLife 2016-02-21

On the basis of multidimensional and comprehensive molecular characterization (including DNA methalylation copy number, RNA, protein expression), we classified 894 renal cell carcinomas (RCCs) various histologic types into nine major genomic subtypes. Site origin within nephron was one determinant in classification, reflecting differences among clear cell, chromophobe, papillary RCC. Widespread changes associated with TFE3 gene fusion or chromatin modifier genes were present a specific...

10.1016/j.celrep.2016.02.024 article EN cc-by Cell Reports 2016-03-01

To investigate the impact of newly identified chromosome 3p21 epigenetic tumor suppressors PBRM1, SETD2, and BAP1 on cancer-specific survival (CSS) 609 patients with clear cell renal carcinoma (ccRCC) from 2 distinct cohorts.Select sequencing 3p 188 who underwent resection primary ccRCC at Memorial Sloan-Kettering Cancer Center (MSKCC) was conducted to interrogate genotype-phenotype associations. These findings were compared analyses genomic clinical dataset our nonoverlapping The Genome...

10.1158/1078-0432.ccr-12-3886 article EN Clinical Cancer Research 2013-04-26

Treatment with immune checkpoint inhibitors (ICI) has demonstrated clinical benefit for a wide range of cancer types. Because only subset patients experience benefit, there is strong need biomarkers that are easily accessible across diverse practice settings. Here, in retrospective cohort study 1714 16 different types treated ICI, we show higher neutrophil-to-lymphocyte ratio (NLR) significantly associated poorer overall and progression-free survival, lower rates response after ICI therapy...

10.1038/s41467-021-20935-9 article EN cc-by Nature Communications 2021-02-01

// Luc G.T. Morris 1,2,* , Nadeem Riaz 1,3* Alexis Desrichard 1 Yasin Şenbabaoğlu 4 A. Ari Hakimi 2 Vladimir Makarov Jorge S. Reis-Filho 1,5 and Timothy Chan 1,3 Human Oncology Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA Department of Surgery, 3 Radiation Oncology, Computational Biology 5 Pathology, * These authors have contributed equally to this work Correspondence to: Morris, email: Chan, Keywords : heterogeneity, evolution, survival, cancer, immune...

10.18632/oncotarget.7067 article EN Oncotarget 2016-01-28

Kidney cancer [or renal cell carcinoma (RCC)] is known as "the internist's tumor" because it has protean systemic manifestations, suggesting that utilizes complex, nonphysiologic metabolic pathways. Given the increasing incidence of this and its lack effective therapeutic targets, we undertook an extensive analysis human RCC tissue employing combined grade-dependent proteomics metabolomics to determine how reprogramming occurring in disease allows escape available approaches. After...

10.1158/0008-5472.can-14-1703 article EN Cancer Research 2015-05-08

Obesity increases risk for clear-cell renal cell carcinoma (ccRCC), yet obese patients appear to experience longer survival than nonobese patients. We examined body mass index (BMI) in relation stage, grade, and cancer-specific mortality (CSM) while considering detection bias, nutritional status, molecular tumor features. Data were available from 2119 ccRCC who underwent surgery at Memorial Sloan-Kettering Cancer Center between 1995 2012. Logistic regression models produced associations BMI...

10.1093/jnci/djt310 article EN JNCI Journal of the National Cancer Institute 2013-11-27

Purpose To investigate associations between computed tomographic (CT) features of clear cell renal carcinoma (RCC) and mutations in VHL, PBRM1, SETD2, KDM5C, or BAP1 genes. Materials Methods The institutional review board approved this retrospective, hypothesis-generating study 233 patients with RCC waived the informed consent requirement. was HIPAA compliant. Three radiologists independently reviewed pretreatment CT images all RCCs without knowledge their genomic profile. One radiologist...

10.1148/radiol.13130663 article EN Radiology 2013-09-13

Abstract Purpose: Rapalogs are allosteric mTOR inhibitors and approved agents for advanced kidney cancer. Reports of clonal heterogeneity in this disease challenge the concept targeted monotherapy, yet a small subset patients derives extended benefit. Our aim was to analyze such outliers explore genomic background extreme rapalog sensitivity context intratumor heterogeneity. Experimental Design: We analyzed archived tumor tissue 5 with renal cell carcinoma, who previously achieved durable...

10.1158/1078-0432.ccr-13-2345 article EN Clinical Cancer Research 2014-03-13
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