| Literature DB >> 33922388 |
Martina Mandarano1, Elena Orecchini2, Guido Bellezza1, Jacopo Vannucci3, Vienna Ludovini4, Sara Baglivo4, Francesca Romana Tofanetti4, Rita Chiari5, Elisabetta Loreti1, Francesco Puma3, Angelo Sidoni1, Maria Laura Belladonna2.
Abstract
The enzyme indoleamine 2,3-dioxygenase 1 (IDO1) degrade tryptophan (Trp) into kynurenine (Kyn) at the initial step of an enzymatic pathway affecting T cell proliferation. IDO1 is highly expressed in various cancer types and associated with poor prognosis. Nevertheless, the serum Kyn/Trp concentration ratio has been suggested as a marker of cancer-associated immune suppression. We measured Kyn and Trp in blood samples of a wide cohort of non-small-cell lung cancer (NSCLC) patients, before they underwent surgery, and analyzed possible correlations of the Kyn/Trp ratio with either IDO1 expression or clinical-pathological parameters. Low Kyn/Trp significantly correlated with low IDO1 expression and never-smoker patients; while high Kyn/Trp was significantly associated with older (≥68 years) patients, advanced tumor stage, and squamous cell carcinoma (Sqcc), rather than the adenocarcinoma (Adc) histotype. Moreover, high Kyn/Trp was associated, among the Adc group, with higher tumor stages (II and III), and, among the Sqcc group, with a high density of tumor-infiltrating lymphocytes. A trend correlating the high Kyn/Trp ratio with the probability of recurrences from NSCLC was also found. In conclusion, high serum Kyn/Trp ratio, associated with clinical and histopathological parameters, may serve as a serum biomarker to optimize risk stratification and therapy of NSCLC patients.Entities:
Keywords: immunohistochemical biomarkers; indoleamine-2,3-dioxygenase 1 (IDO1); kynurenine/tryptophan (Kyn/Trp) ratio; non-small cell lung cancer (NSCLC); serum biomarkers
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Year: 2021 PMID: 33922388 DOI: 10.3390/ijms22094403
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923