Monitoring of low-molecular
weight cancer biomarkers, such as tryptophan
(Trp) and its derivative kynurenine (Kyn), might be advantageous to
non-invasive skin cancer detection. Thus, we assessed several approaches
of topical sampling of Trp and Kyn, in relation to phenylalanine (Phe)
and tyrosine (Tyr), on the volar forearm of six healthy volunteers.
The sampling was performed with three hydrogels (made of agarose or/and
chitosan), hydrated starch films, cotton swabs, and tape stripping.
The biomarkers were successfully sampled by all approaches, but the
amount of collected Kyn was low, 20 ± 10 pmol/cm
2
.
Kyn quantification was below LOQ, and thus, it was detected only in
20% of topical samples. To mitigate variability problems of absolute
amounts of sampled amino acids, Tyr/Trp, Phe/Trp, and Phe/Tyr ratios
were assessed, proving reduced inter-individual variation from 79
to 45% and intra-individual variation from 42 to 21%. Strong positive
correlation was found between Phe and Trp, pointing to the Phe/Trp
ratio (being in the 1.0–2.0 range, at 95% confidence) being
least dependent on sampling materials, approaches, and sweating. This
study leads to conclusion that due to the difficulty in quantifying
less abundant Kyn, and thus the Trp/Kyn ratio, the Phe/Trp ratio might
be a possible, alternative biomarker for detecting skin cancers.