Friday 27 April 2018

Biomarkers for the diagnosis of the gastrointestinal (GI) cancers


Lower GI cancers are among the top three most frequent cancers in the United States and many western countries while upper GI cancers rank as the most prevalent type in many Asian countries, especially in central and eastern Asia. GI cancers are usually diagnosed in more advanced stages and in the absence of effective early diagnostic tools and therapeutic modalities, the survival rates are generally disappointingly low. Then the era of biomarkers came to solve the issue of the GI Cancer diagnosis.

Biomarker refers to a measurable indicator of some biological state or condition. This is also referring to a substance whose detection indicates the existence of a living organism. This is also used to evaluate or to examine normal biological processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention.

Currently, serum biomarkers, which are sufficiently sensitive and specific for early detection and risk classification of gastric cancers. In future Three-dimensional combined biomarkers assay could improve diagnostic accuracy for gastric cancer. For cancer research MicroRNAs (miRNAs) have become the center of focus. However, there have been inconsistencies in the literature regarding the suitability of circulating miRNAs for early detection of gastrointestinal cancers.

Last few years major advances have been made to understand the role of epigenetic alterations in carcinogenesis, particularly for DNA methylation, histone modifications and non-coding RNAs. Aberrant hypermethylation of DNA at CpG islands is a well-established phenomenon that mediates transcriptional silencing of tumor suppressor genes, and it is an early event integral to gastrointestinal cancer development.

As such, detection of aberrant DNA methylation is being developed as biomarkers for prognostic and diagnostic purposes in gastrointestinal cancers. Diverse tissue types are suitable for the analyses of methylated DNA, such as tumor tissues, blood, plasma, and stool, and some of these markers are already utilized in the clinical setting.

Recent advances in the genome-wide epigenomic approaches are enabling the comprehensive mapping of the cancer methylome, thus providing new avenues for mining novel biomarkers for disease prognosis and diagnosis.

The biomarkers in GI cancers are useful not only for screening, diagnosis, and prognosis but also for prediction of the response to mechanism-based interventions, such as chemoprevention. On-going assessment of these diagnostic and predictive factors will probably lead to a change in the current staging of many GI cancers.



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