"The next obvious question is “Are we there yet?”
The answer is, “Close,
if not completely there”. Without any doubt, recent studies have
provided tangible evidence that distinct methylation profiles of DNA
originating from tumor cells can be effectively used to screen for
occult neoplasia. As described earlier, epigenetic biomarkers offer a
plethora of distinct advantages over genetic markers, and de novo
methylation represents a positive signal that can be readily detected
and quantified in the background of unmethylated alleles. Therefore,
despite the current enthusiasm and rapid progress in the field, it may
be some time before epigenetic biomarkers are routinely employed. In the
interim, the burden lies on the basic researchers and clinicians to
continue to identify and validate the repertoire of potential fecal
DNA-methylation biomarkers. To reap the full benefits of what we have
learnt thus far will eventually require the deciphering of a panel of
biomarkers that are highly specific, sufficiently robust and facile,
inexpensive and ready for the ‘prime-time’ screening of mass populations
at risk for GI cancers. None of this may bear the expected results if
we fail to educate the population about the perks and the need for
screening, break the cultural taboos and overcome the financial
roadblocks that are responsible for low compliance rates. Lastly, steps
should be taken to design adequate clinical trials and build a business
model that can be used for commercialization of newly discovered fecal
DNA methylation biomarkers. These efforts will hasten the translation of
genomic discoveries into clinical practice in the not-so-distant
future."
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