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.

Kynurenine/Tryptophan Ratio as a Potential Blood-Based Biomarker in Non-Small Cell Lung Cancer / Mandarano, Martina; Orecchini, Elena; Bellezza, Guido; Vannucci, Jacopo; Ludovini, Vienna; Baglivo, Sara; Tofanetti, Francesca Romana; Chiari, Rita; Loreti, Elisabetta; Puma, Francesco; Sidoni, Angelo; Belladonna, Maria Laura. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1422-0067. - 22:9(2021). [10.3390/ijms22094403]

Kynurenine/Tryptophan Ratio as a Potential Blood-Based Biomarker in Non-Small Cell Lung Cancer

Vannucci, Jacopo;
2021

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.
2021
immunohistochemical biomarkers; indoleamine-2,3-dioxygenase 1 (IDO1); kynurenine/tryptophan (Kyn/Trp) ratio; non-small cell lung cancer (NSCLC); serum biomarkers; adenocarcinoma of lung; adult; aged; aged, 80 and over; B7-H1 antigen; biomarkers, tumor; carcinoma, non-small-cell lung; carcinoma, squamous cell; female; follow-up studies; humans; indoleamine-pyrrole 2,3,-dioxygenase; kynurenine; lung neoplasms; lymphocytes, tumor-infiltrating; male; middle aged; neoplasm recurrence, local; prognosis; survival rate; tryptophan
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Kynurenine/Tryptophan Ratio as a Potential Blood-Based Biomarker in Non-Small Cell Lung Cancer / Mandarano, Martina; Orecchini, Elena; Bellezza, Guido; Vannucci, Jacopo; Ludovini, Vienna; Baglivo, Sara; Tofanetti, Francesca Romana; Chiari, Rita; Loreti, Elisabetta; Puma, Francesco; Sidoni, Angelo; Belladonna, Maria Laura. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1422-0067. - 22:9(2021). [10.3390/ijms22094403]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1660546
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