Detection of Chromosomal Alterations in the Circulation of Cancer Patients with Whole-Genome Sequencing

被引:500
作者
Leary, Rebecca J. [1 ,2 ]
Sausen, Mark [1 ,2 ]
Kinde, Isaac [1 ,2 ]
Papadopoulos, Nickolas [1 ,2 ]
Carpten, John D. [3 ]
Craig, David [3 ]
O'Shaughnessy, Joyce [4 ]
Kinzler, Kenneth W. [1 ,2 ]
Parmigiani, Giovanni [5 ,6 ]
Vogelstein, Bert [1 ,2 ]
Diaz, Luis A., Jr. [1 ,2 ]
Velculescu, Victor E. [1 ,2 ]
机构
[1] Johns Hopkins Kimmel Canc Ctr, Ludwig Ctr Canc Genet, Baltimore, MD 21287 USA
[2] Johns Hopkins Kimmel Canc Ctr, Howard Hughes Med Inst, Baltimore, MD 21287 USA
[3] Translat Genom Res Inst, Phoenix, AZ 85044 USA
[4] US Oncol, Texas Oncol, Baylor Sammons Canc Ctr, Dallas, TX 75246 USA
[5] Dana Farber Canc Inst, Dept Biostat & Comp Biol, Boston, MA 02215 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
关键词
MINIMAL RESIDUAL DISEASE; ACUTE LYMPHOBLASTIC-LEUKEMIA; DETECTABLE CLONAL MOSAICISM; COPY-NUMBER; MUTATIONS; REARRANGEMENTS; PLASMA; BREAST; DNA; IDENTIFICATION;
D O I
10.1126/scitranslmed.3004742
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clinical management of cancer patients could be improved through the development of noninvasive approaches for the detection of incipient, residual, and recurrent tumors. We describe an approach to directly identify tumor-derived chromosomal alterations through analysis of circulating cell-free DNA from cancer patients. Whole-genome analyses of DNA from the plasma of 10 colorectal and breast cancer patients and 10 healthy individuals with massively parallel sequencing identified, in all patients, structural alterations that were not present in plasma DNA from healthy subjects. Detected alterations comprised chromosomal copy number changes and rearrangements, including amplification of cancer driver genes such as ERBB2 and CDK6. The level of circulating tumor DNA in the cancer patients ranged from 1.4 to 47.9%. The sensitivity and specificity of this approach are dependent on the amount of sequence data obtained and are derived from the fact that most cancers harbor multiple chromosomal alterations, each of which is unlikely to be present in normal cells. Given that chromosomal abnormalities are present in nearly all human cancers, this approach represents a useful method for the noninvasive detection of human tumors that is not dependent on the availability of tumor biopsies.
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页数:12
相关论文
共 42 条
[11]   Circulating mutant DNA to assess tumor dynamics [J].
Diehl, Frank ;
Schmidt, Kerstin ;
Choti, Michael A. ;
Romans, Katharine ;
Goodman, Steven ;
Li, Meng ;
Thornton, Katherine ;
Agrawal, Nishant ;
Sokoll, Lori ;
Szabo, Steve A. ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Diaz, Luis A., Jr. .
NATURE MEDICINE, 2008, 14 (09) :985-990
[12]   Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood [J].
Fan, H. Christina ;
Blumenfeld, Yair J. ;
Chitkara, Usha ;
Hudgins, Louanne ;
Quake, Stephen R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (42) :16266-16271
[13]   Sensitivity of Noninvasive Prenatal Detection of Fetal Aneuploidy from Maternal Plasma Using Shotgun Sequencing Is Limited Only by Counting Statistics [J].
Fan, H. Christina ;
Quake, Stephen R. .
PLOS ONE, 2010, 5 (05)
[14]   Noninvasive Identification and Monitoring of Cancer Mutations by Targeted Deep Sequencing of Plasma DNA [J].
Forshew, Tim ;
Murtaza, Muhammed ;
Parkinson, Christine ;
Gale, Davina ;
Tsui, Dana W. Y. ;
Kaper, Fiona ;
Dawson, Sarah-Jane ;
Piskorz, Anna M. ;
Jimenez-Linan, Mercedes ;
Bentley, David ;
Hadfield, James ;
May, Andrew P. ;
Caldas, Carlos ;
Brenton, James D. ;
Rosenfeld, Nitzan .
SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (136)
[15]   Prospective Minimal Residual Disease Monitoring to Predict Relapse of Acute Promyelocytic Leukemia and to Direct Pre-Emptive Arsenic Trioxide Therapy [J].
Grimwade, David ;
Jovanovic, Jelena V. ;
Hills, Robert K. ;
Nugent, Elizabeth A. ;
Patel, Yashma ;
Flora, Rajinder ;
Diverio, Daniela ;
Jones, Katy ;
Aslett, Hannah ;
Batson, Elaine ;
Rennie, Kristian ;
Angell, Roger ;
Clark, Richard E. ;
Solomon, Ellen ;
Lo-Coco, Francesco ;
Wheatley, Keith ;
Burnett, Alan K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (22) :3650-3658
[16]  
He J, 2011, ONCOTARGET, V2, P178
[17]   Monitoring CML patients responding to treatment with tyrosine kinase inhibitors:: review and recommendations for harmonizing current methodology for detecting BCR-ABL transcripts and kinase domain mutations and for expressing results [J].
Hughes, Timothy ;
Deininger, Michael ;
Hochhaus, Andreas ;
Branford, Susan ;
Radich, Jerald ;
Kaecla, Jaspal ;
Baccarani, Michele ;
Cortes, Jorge ;
Cross, Nicholas C. P. ;
Druker, Brian J. ;
Gabert, Jean ;
Grimwade, David ;
Hehlmann, Ruediger ;
Kamel-Reid, Suzanne ;
Lipton, Jeffrey H. ;
Longtine, Janina ;
Martinelli, Giovanni ;
Saglio, Giuseppe ;
Soverini, Simona ;
Stock, Wendy ;
Goldman, John M. .
BLOOD, 2006, 108 (01) :28-37
[18]   Detection of large-scale variation in the human genome [J].
Iafrate, AJ ;
Feuk, L ;
Rivera, MN ;
Listewnik, ML ;
Donahoe, PK ;
Qi, Y ;
Scherer, SW ;
Lee, C .
NATURE GENETICS, 2004, 36 (09) :949-951
[19]   Detectable clonal mosaicism and its relationship to aging and cancer [J].
Jacobs, Kevin B. ;
Yeager, Meredith ;
Zhou, Weiyin ;
Wacholder, Sholom ;
Wang, Zhaoming ;
Rodriguez-Santiago, Benjamin ;
Hutchinson, Amy ;
Deng, Xiang ;
Liu, Chenwei ;
Horner, Marie-Josephe ;
Cullen, Michael ;
Epstein, Caroline G. ;
Burdett, Laurie ;
Dean, Michael C. ;
Chatterjee, Nilanjan ;
Sampson, Joshua ;
Chung, Charles C. ;
Kovaks, Joseph ;
Gapstur, Susan M. ;
Stevens, Victoria L. ;
Teras, Lauren T. ;
Gaudet, Mia M. ;
Albanes, Demetrius ;
Weinstein, Stephanie J. ;
Virtamo, Jarmo ;
Taylor, Philip R. ;
Freedman, Neal D. ;
Abnet, Christian C. ;
Goldstein, Alisa M. ;
Hu, Nan ;
Yu, Kai ;
Yuan, Jian-Min ;
Liao, Linda ;
Ding, Ti ;
Qiao, You-Lin ;
Gao, Yu-Tang ;
Koh, Woon-Puay ;
Xiang, Yong-Bing ;
Tang, Ze-Zhong ;
Fan, Jin-Hu ;
Aldrich, Melinda C. ;
Amos, Christopher ;
Blot, William J. ;
Bock, Cathryn H. ;
Gillanders, Elizabeth M. ;
Harris, Curtis C. ;
Haiman, Christopher A. ;
Henderson, Brian E. ;
Kolonel, Laurence N. ;
Le Marchand, Loic .
NATURE GENETICS, 2012, 44 (06) :651-U68
[20]  
Kent WJ, 2002, GENOME RES, V12, P656, DOI [10.1101/gr.229202, 10.1101/gr.229202. Article published online before March 2002]