Use of nanotechnology for the development of novel cancer biomarkers

被引:11
作者
Banerjee, Hirendra Nath
Verma, Mukesh
机构
[1] Univ N Carolina, Dept Biol Sci & Pharmaceut Sci, Div Math Sci Technol & Pharmaceut Sci, Elizabeth City State Univ, Elizabeth City, NC 27909 USA
[2] NCI, Epidemiol & Genet Res Program, Div Canc Control & Populat Sci, Bethesda, MD 20892 USA
关键词
microarray; nanomedicine; raman spectroscopy; surface enhanced laser desorption/ionization;
D O I
10.1586/14737159.6.5.679
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Novel nanotechnologies can complement and augment existing genomic and proteomic techniques employed to analyze variations across different tumor types, thus offering the potential to distinguish between normal and malignant cells. Sensitive biosensors constructed out of nanoscale components (e.g., nanocantilevers, nanowires and nanochannels) can recognize genetic and molecular events and have reporting capabilities, thereby offering the potential to detect rare molecular signals associated with malignancy. Such signals may then be collected for analysis by nanoscale harvesters that selectively isolate cancer-related molecules from tissues. Another area with near-term potential for the early detection of cancer is the identification of mutations and genomic instability.
引用
收藏
页码:679 / 683
页数:5
相关论文
共 25 条
  • [1] Banerjee H, 2004, CELL MOL BIOL, V50, P733
  • [2] Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray
    Borsting, C
    Sanchez, JJ
    Morling, N
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2004, 118 (02) : 75 - 82
  • [3] Optical trapping of a spherically symmetric sphere in the ray-optics regime: a model for optical tweezers upon cells
    Chang, Yi-Ren
    Hsu, Long
    Chi, Sien
    [J]. APPLIED OPTICS, 2006, 45 (16) : 3885 - 3892
  • [4] Treatment-specific changes in gene expression discriminate in vivo drug response in human leukemia cells
    Cheok, MH
    Yang, WL
    Pui, CH
    Downing, JR
    Cheng, C
    Naeve, CW
    Relling, MV
    Evans, WE
    [J]. NATURE GENETICS, 2003, 34 (01) : 85 - 90
  • [5] Comparison of two CYP2D6 genotyping methods and assessment of genotype-phenotype relationships
    Chou, WH
    Yan, FX
    Robbins-Weilert, DK
    Ryder, TB
    Liu, WW
    Perbost, C
    Fairchild, M
    de Leon, J
    Koch, WH
    Wedlund, PJ
    [J]. CLINICAL CHEMISTRY, 2003, 49 (04) : 542 - 551
  • [6] Identifying Mycobacterium species and strain typing using a microfluidic labchip instrument
    Cooksey, RC
    Limor, J
    Morlock, GP
    Crawford, J
    [J]. BIOTECHNIQUES, 2003, 35 (04) : 786 - 794
  • [7] Classification of bladder cancer by microarray expression profiling: towards a general clinical use of microarrays in cancer diagnostics
    Dyrskjot, L
    [J]. EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2003, 3 (05) : 635 - 647
  • [8] Molecular diagnostics by microelectronic microchips
    Ferrari, M
    Stenirri, S
    Bonini, P
    Cremonesi, L
    [J]. CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2003, 41 (04) : 462 - 467
  • [9] Nanodiagnostics: application of nanotechnology in molecular diagnostics
    Jain, KK
    [J]. EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2003, 3 (02) : 153 - 161
  • [10] Crystal structure and molecular modeling of 17-DMAG in complex with human Hsp90
    Jez, JM
    Chen, JCH
    Rastelli, G
    Stroud, RM
    Santi, DV
    [J]. CHEMISTRY & BIOLOGY, 2003, 10 (04): : 361 - 368