Direct Profiling of Cancer Biomarkers in Tumor Tissue Using a Multiplexed Nanostructured Microelectrode Integrated Circuit

被引:70
作者
Fang, Zhichao [1 ]
Soleymani, Leyla [2 ]
Pampalakis, Georgios [1 ]
Yoshimoto, Maisa [3 ]
Squire, Jeremy A. [3 ]
Sargent, Edward H. [2 ]
Kelley, Shana O. [1 ,4 ]
机构
[1] Univ Toronto, Dept Pharmaceut Sci, Leslie Dan Fac Pharm, Toronto, ON, Canada
[2] Univ Toronto, Fac Engn, Dept Elect & Comp Engn, Toronto, ON, Canada
[3] Queens Univ, Dept Pathol & Mol Med, Kingston, ON, Canada
[4] Univ Toronto, Dept Biochem, Fac Med, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
electrochemical biosensing; nanostructures; biomarker; diagnostic; microchip; LABEL-FREE DETECTION; PROSTATE-CANCER; ELECTRICAL DETECTION; ELECTROCHEMICAL DETECTION; NANOWIRE NANOSENSORS; DNA HYBRIDIZATION; SENSORS; FUSION; ARRAYS; SPECTROSCOPY;
D O I
10.1021/nn900733d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The analysis of panels of nucleic acid biomarkers offers valuable diagnostic and prognostic information for cancer management, A cost-effective, highly sensitive electronic chip would offer an ideal platform for clinical biomarker readout and would have maximal utility if it was (i) multiplexed, enabling on-chip assays of multiple biomarkers, and (ii) able to perform direct (PCR-free) readout of disease-related genes. Here we report a chip onto which we integrate novel nanostructured microelectrodes and with which we directly detect cancer biomarkers in heterogeneous biological samples-both cell extracts and tumor tissues. Coarse photolithographic microfabrication defines a multiplexed sensing array; bottom-up fabrication of nanostructured microelectrodes then provides sensing elements. We analyzed a panel of mRNA samples for prostate cancer related gene fusions using the chip. We accurately identified gene fusions that correlate with aggressive prostate cancer and distinguished these from fusions associated with slower-progressing forms of the disease. The multiplexed nanostructured microelectrode integrated circuit reported herein provides direct, amplification-free, sample-to-answer in under 1 h using the 10 ng of mRNA readily available in biopsy samples.
引用
收藏
页码:3207 / 3213
页数:7
相关论文
共 31 条
[1]   Predicting disease using genomics [J].
Bell, J .
NATURE, 2004, 429 (6990) :453-456
[2]   Nanowire nanosensors for highly sensitive and selective detection of biological and chemical species [J].
Cui, Y ;
Wei, QQ ;
Park, HK ;
Lieber, CM .
SCIENCE, 2001, 293 (5533) :1289-1292
[3]   Electrochemical DNA sensors [J].
Drummond, TG ;
Hill, MG ;
Barton, JK .
NATURE BIOTECHNOLOGY, 2003, 21 (10) :1192-1199
[4]   Direct Electrocatalytic mRNA Detection Using PNA-Nanowire Sensors [J].
Fang, Zhichao ;
Kelley, Shana O. .
ANALYTICAL CHEMISTRY, 2009, 81 (02) :612-617
[5]   Silicon nanowire arrays for label-free detection of DNA [J].
Gao, Zhiqiang ;
Agarwal, Ajay ;
Trigg, Alastair D. ;
Singh, Navab ;
Fang, Cheng ;
Tung, Chih-Hang ;
Fan, Yi ;
Buddharaju, Kavitha D. ;
Kong, Jinming .
ANALYTICAL CHEMISTRY, 2007, 79 (09) :3291-3297
[6]   Ultrasensitive electrocatalytic DNA detection at two- and three-dimensional nanoelectrodes [J].
Gasparac, R ;
Taft, BJ ;
Lapierre-Devlin, MA ;
Lazareck, AD ;
Xu, JM ;
Kelley, SO .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (39) :12270-12271
[7]   Direct ultrasensitive electrical detection of DNA and DNA sequence variations using nanowire nanosensors [J].
Hahm, J ;
Lieber, CM .
NANO LETTERS, 2004, 4 (01) :51-54
[8]   Probing biomolecular interactions at conductive and semiconductive surfaces by impedance spectroscopy: Routes to impedimetric immunosensors, DNA-Sensors, and enzyme biosensors [J].
Katz, E ;
Willner, I .
ELECTROANALYSIS, 2003, 15 (11) :913-947
[9]   Electroactive chitosan nanoparticles for the detection of single-nucleotide polymorphisms using peptide nucleic acids [J].
Kerman, Kagan ;
Saito, Masato ;
Tamiya, Eiichi .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2008, 391 (08) :2759-2767
[10]   Recurrent gene fusions in prostate cancer [J].
Kumar-Sinha, Chandan ;
Tomlins, Scott A. ;
Chinnaiyan, Arul M. .
NATURE REVIEWS CANCER, 2008, 8 (07) :497-511