Measurement of biomarker proteins for point-of-care early detection and monitoring of cancer

被引:432
作者
Rusling, James F. [1 ,2 ,4 ]
Kumar, Challa V. [1 ,3 ]
Gutkind, J. Silvio [5 ]
Patel, Vyomesh [5 ]
机构
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Univ Connecticut, Ctr Hlth, Dept Cell Biol, Farmington, CT 06032 USA
[3] Univ Connecticut, Dept Mol & Cell Biol, Storrs, CT 06269 USA
[4] Natl Univ Ireland, Sch Chem, Galway, Ireland
[5] Natl Inst Dent & Craniofacial Res, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD 20892 USA
基金
爱尔兰科学基金会; 美国国家科学基金会;
关键词
ROLLING-CIRCLE AMPLIFICATION; PROSTATE-SPECIFIC ANTIGEN; CARBON NANOTUBE FOREST; ELECTROCHEMICAL IMMUNOSENSORS; YEAST ISO-1-CYTOCHROME-C; MULTIPLEXED DETECTION; HUMAN-PAPILLOMAVIRUS; PROTEOMIC ANALYSIS; ANTIBODY ARRAYS; OVARIAN-CANCER;
D O I
10.1039/c0an00204f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This critical review evaluates progress toward viable point-of-care protein biomarker measurements for cancer detection and diagnostics. The ability to measure panels of specific, selective cancer biomarker proteins in physicians' surgeries and clinics has the potential to revolutionize cancer detection, monitoring, and therapy. The dream envisions reliable, cheap, automated, technically undemanding devices that can analyze a patient's serum or saliva in a clinical setting, allowing on-the-spot diagnosis. Existing commercial products for protein assays are reliable in laboratory settings, but have limitations for point-of-care applications. A number of ultrasensitive immunosensors and some arrays have been developed, many based on nanotechnology. Multilabel detection coupled with high capture molecule density in immunosensors and arrays seems to be capable of detecting a wide range of protein concentrations with sensitivity ranging into the sub pg mL(-1) level. Multilabel arrays can be designed to detect both high and ultralow abundance proteins in the same sample. However, only a few of the newer ultrasensitive methods have been evaluated with real patient samples, which is key to establishing clinical sensitivity and selectivity.
引用
收藏
页码:2496 / 2511
页数:16
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