Publication: Research - peer-review › Conference article – Annual report year: 2010
Cancer is a leading cause of death worldwide. Resistance of tumor cells to radiation and chemotherapy is the major obstacle in cancer treatment. The serious toxicity that follows the administration of certain drugs can be associated with Single Nucleotide Polymorphisms (SNPs) of genes involved in drug metabolism and can ultimately reduce the clinical efficacy of chemotherapy. The KRAS and TP53 genes are altered in many human tumors. K-RAS point mutation appear early in the tumorigenesis pathway and can therefore be used for early cancer detection. The functional inactivation of p53 by point mutation is a hallmark of many tumors. Importantly, most anticancer agents act by inducing apoptosis and, typically, p53- deficient tumors are more resistant to drug-induced apoptosis than those carrying wild-type p53. It is therefore important to analyze such SNPs and point mutation in cancer diagnosis and treatment. In this paper, we described a total integrated BIOLABCHIP namely SMART-BioMEMS for rapid detection and identification SNPs of Kirsten-RAS (K-ras) and TP53 genes in cancer. The SMART-BioMEMS system consist of different components: An optical readout system, disposable biochip; and a reusable actuators chip that can perform all the steps from sample preparation, DNA isolation and purification, PCR amplification, Enzymatic clean up, mini-sequencing and SNP detection. The prototype of the SmartBIOMEMS system designs, detail of different components and functions will be present and discusses. It is results of great cooperation in the FP6 EU project SMART-BioMEMS. © Springer-Verlag 2010.
|Conference||3rd International Conference on the Development of Biomedical Engineering in Vietnam|
|City||Ho Chi Minh City|
|Period||01/01/10 → …|
|Citations||Web of Science® Times Cited: No match on DOI|
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