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An introduction to the dna chips and the pharmaceutical industry

This article has been cited by other articles in PMC. Abstract Microarray is an introduction to the dna chips and the pharmaceutical industry of the most recent advances being used for cancer research; it provides assistance in pharmacological approach to treat various diseases including oral lesions. Microarray helps in analyzing large amount of samples which have either been recorded previously or new samples; it even helps to test the incidence of a particular marker in tumors.

Till recently, microarray's usage in dentistry has been very limited, but in future, as the technology becomes affordable, there may be increase in its usage. Here, we discuss the various techniques and applications of microarray or DNA chip.

Cancer, human genome, microarray, tissue microarray Once the human genome sequence was completed in 2001, it paved the way for many experiments and researches; one such area was identifying the regions of DNA which control normal and disease states.

Functional genomics is the study of gene function through parallel expression measurements of a genome. The most common tools used to carry out these measurements include complementary DNA microarrays, oligonucleotide microarrays, or serial analysis of gene expression SAGE. Microarray analysis can be divided into two main steps: Specific sequences are immobilized to a surface and reacted with labeled cDNA targets.

A signal resulting from hybridization of the labeled target with the specific immobilized probe identifies which RNAs are present in the unknown target sample. Prevention, diagnosis, and treatment in dental practice are based on an understanding of the biology of underlying oral health and disease. Few aspects of patient care will remain untouched by today's rapid advances in biological research.

In the future, dentists may use inexpensive but remarkably sophisticated diagnostic tests to diagnose infection, oral lesions, and symptoms of temporomandibular dysfunction TMD.

Microarray and its applications

The small variations in the DNA sequence that lead to different characteristics such as skin color, facial features, or height are known as polymorphisms, which also can cause or contribute to the development of many syndromes and diseases. Microarray provides a basis to genotype thousands of different loci at a time, which is useful for association and linkage studies to isolate chromosomal regions related to a particular disease.

An introduction to the dna chips and the pharmaceutical industry

This array also can be used to locate chromosomal aberrations related to cancer, such as segments of allelic imbalance, which can be identified by loss of heterozygosity. The different DNA fragments are arranged in rows and columns such that the identity of each fragment is known through its location on the array.

Two types of microarrays are gene expression microarray and tissue microarray TMA. Techniques like Northern blot and reverse transcriptase-polymerase chain reaction RT-PCR allow testing for only a few genes per experiment. Microarray Principle mRNA is an intermediary molecule which carries the genetic information from the cell nucleus to the cytoplasm for protein synthesis.

Whenever some genes are expressed or are in their active state, many copies of mRNA corresponding to the particular genes are produced by a process called transcription.

These mRNAs synthesize the corresponding protein by translation.

So, indirectly by assessing the various mRNAs, we can assess the genetic information or the gene expression. This helps in the understanding of various processes behind every altered genetic expression. Thus, mRNA acts as a surrogate marker.

The principle behind microarrays is that complementary sequences will bind to each other. The unknown DNA molecules are cut into fragments by restriction endonucleases; fluorescent markers are attached to these DNA fragments.

These are then allowed to react with probes of the DNA chip. The remaining DNA fragments are washed away. The target DNA pieces can be identified by their fluorescence emission by passing a laser beam.

A computer is used to record the pattern of fluorescence emission and DNA identification. This technique of employing DNA chips is very rapid, besides being sensitive and specific for the identification of several DNA fragments simultaneously. TMAs are similar to gene expression microarrays in having samples arrayed in rows and columns on a glass slide; they differ in that each element on the TMA slide corresponds to a single patient sample, allowing multiple patient samples to be assessed for a single molecular marker in one experiment, while gene expression arrays allow assessment of thousands of molecular markers on a single patient sample per experiment.

Applications In cancer Tumor formation involves simultaneous changes in hundreds of cells and variations in genes. An introduction to the dna chips and the pharmaceutical industry can be a boon to researchers as it provides a platform for simultaneous testing of a large set of genetic samples. It helps especially in the identification of single-nucleotide polymorphisms SNPs and mutations, classification of tumors, identification of target genes of tumor suppressors, identification of cancer biomarkers, identification of genes associated with chemoresistance, and drug discovery.

For example, we can compare the different patterns of gene expression levels between a group of cancer patients and a group of normal patients and identify the gene associated with that particular cancer. Gene microarrays have been used for comparative genomic hybridization.

In this technique, genomic DNA is fluorescently labeled and used to determine the presence of gene loss or amplification.

The conversion of a non-invasive tumor to an invasive tumor also warrants research. Microarray-based expression profiling allows us to identity families of genes as well as the important molecular and cellular events that might be important in complex processes like metastasis. Practical applications in future include diagnostic and prognostic management of patients.

Clinicians will be able to use microarrays during early clinical trials to confirm the mechanisms of action of drugs and to assess drug sensitivity and toxicity. They can be used to develop a new molecular taxonomy of cancer, including clustering of cancers according to prognostic groups on the basis of gene expression profiles. Antibiotic treatment Increase in the number of resistant bacteria and superadded infections has led to failure of antibiotics.

Virulence of the bacterial strains too affects the outcome of the disease process. In oral cavity where anaerobic bacteria might be the infective agent, they often are not easily culturable, especially organisms such as actinomyces.

DNA microarray analysis helps as the bacterial genomic DNA often outlasts the viability of the bacteria and a diagnosis can be made using a small amount of DNA, as opposed to the large numbers of bacteria needed for culture.

In future, an abscess specimen might be sent not for culture and sensitivity testing, but rather for DNA microarray analysis. Early detection of oral precancerous lesions Leukoplakia or white lesions of the oral cavity may result from a myriad of reversible conditions.

  • In one of the meetings of the Affymax scientific board, Leighton Read tossed out the idea of just mimicking the makers of semiconductor chips, who use beams of light to manipulate molecules on solid surfaces in order to create random chemical diversity;
  • Antibiotic treatment Increase in the number of resistant bacteria and superadded infections has led to failure of antibiotics;
  • The next step for the group was to begin work on implementing the idea of generating chemical diversity on an array designed by a photolithographic process;
  • The typical story told about the role of federal funding emphasizes the spillovers from federally funded academic research to industry.

Currently, microscopic examination fails to identify the small subset of these lesions that progress to oral cancer. Recent studies have illustrated the effectiveness of microarrays in oral cancer. Early diagnosis and management of oral cancer is correlated with increased survival.

Identification and treatment of premalignant and early cancerous oral lesions may become one of the most valuable services in future performs. Conclusion This review has given a small outline of the technique behind microarray and the various steps involved. The technique, though limited at present in its applications due to the cost factor, may widen its prospects once there is increase in the availability of commercial products.

The ability to record large number of old samples and analyzing them for various genetic alterations helps in understanding the concept of molecular biology. Microarrays hold much promise for the analysis of diseases in the oral cavity. Classifications of oral disease by DNA, RNA, or protein profiles will greatly enhance our ability to diagnose, prevent, monitor and treat our patients.

The emergence and diffusion of DNA microarray technology

Currently, microarrays are primarily a research tool. Microarrays promise a more biologically based, individualized, and vastly improved standard for oral care, which will have great clinical impact on the way dentistry will be practiced in the future.

Footnotes Conflict of Interest: Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Loss of heterozygosity analysis of small-cell lung carcinomas using single nucleotide polymorphism arrays. Accumulative increase of loss of heterozygosity from leukoplakia to foci of early cancerization in leukoplakia of the oral cavity.

Brown PO, Botstein D. Exploring the new world of the genome with DNA microarrays. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Tissue microarrays for high-throughput molecular profiling of tumor specimens. Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors.

Biochips to screen for genomic imbalances. Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors. Genome-wide arraybased comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in fallopian tube carcinoma.

Determination of amplicon boundaries at 20q13. A fullcoverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.

Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations. Pascale F, Macgregor, Jeremy A. Squire, Application of microarrays to the analysis of gene expression in cancer.

Oral cancer in vivo gene expression profiling assisted by laser capture microdissection and microarray analysis. Gene expression levels in different stages of progression in oral squamous cell carcinoma.