Carbonic anhydrase (CA, EC 4.2.1.1) IX is regarded as a tumour hypoxia marker and CA inhibitors have been proposed as a new class of antitumor agents, with one such agent in Phase II clinical trials. The expression of some CAs, in particular the isoforms CA IX and CA XII, has been correlated with tumor aggressiveness and progression in several cancers. The aim of this study was to evaluate the possibility that CA IX could represent a marker related to clear cell Renal Cell Carcinoma (ccRCC). Bcl-2 and Bax, and the activity of caspase-3, evaluated in tissue biopsies from patients, were congruent with resistance to apoptosis in ccRCCs with respect to healthy controls, respectively. In the same samples, the CA IX and pro-angiogenic factor VEGF expressions revealed that both these hypoxia responsive proteins were strongly increased in ccRCC with respect to controls. C AIX plasma concentration and CA activity were assessed in healthy volunteers and patients with benign kidney tumors and ccRCCs. CA IX expression levels were found strongly increased only in plasma from ccRCC subjects, whereas CA activity was found similarly increased both in plasma from ccRCC and benign tumor patients, compared to healthy volunteers. These results show that the plasmatic level of CA IX, but not the CA total activity, can be considered a diagnostic marker of ccRCCs. Furthermore, as many reports exist relating CA IX inhibition to a better outcome to anticancer therapy in ccRCC, plasma levels of CA IX could be also predictive for response to therapy.

PLASMATIC CARBONIC ANHYDRASE IX AS A DIAGNOSTIC MARKER FOR CLEAR CELL RENAL CELL CARCINOMA / Lucarini, Laura; Magnelli, Lucia; Schiavone, Nicola; Crisci, Alfonso; Innocenti, Alessio; Puccetti, Luca; Cianchi, Fabio; Peri, Sara; Supuran, CLAUDIU TRANDAFIR; Papucci, Laura; Masini, Emanuela;. - In: JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY. - ISSN 1475-6366. - ELETTRONICO. - 33:(2017), pp. 234-240. [10.1080/14756366.2017.1411350]

PLASMATIC CARBONIC ANHYDRASE IX AS A DIAGNOSTIC MARKER FOR CLEAR CELL RENAL CELL CARCINOMA

Lucarini, Laura;Magnelli, Lucia;Schiavone, Nicola;Crisci, Alfonso;Cianchi, Fabio;Peri, Sara;Supuran, CLAUDIU TRANDAFIR;Papucci, Laura
;
Masini, Emanuela
2017

Abstract

Carbonic anhydrase (CA, EC 4.2.1.1) IX is regarded as a tumour hypoxia marker and CA inhibitors have been proposed as a new class of antitumor agents, with one such agent in Phase II clinical trials. The expression of some CAs, in particular the isoforms CA IX and CA XII, has been correlated with tumor aggressiveness and progression in several cancers. The aim of this study was to evaluate the possibility that CA IX could represent a marker related to clear cell Renal Cell Carcinoma (ccRCC). Bcl-2 and Bax, and the activity of caspase-3, evaluated in tissue biopsies from patients, were congruent with resistance to apoptosis in ccRCCs with respect to healthy controls, respectively. In the same samples, the CA IX and pro-angiogenic factor VEGF expressions revealed that both these hypoxia responsive proteins were strongly increased in ccRCC with respect to controls. C AIX plasma concentration and CA activity were assessed in healthy volunteers and patients with benign kidney tumors and ccRCCs. CA IX expression levels were found strongly increased only in plasma from ccRCC subjects, whereas CA activity was found similarly increased both in plasma from ccRCC and benign tumor patients, compared to healthy volunteers. These results show that the plasmatic level of CA IX, but not the CA total activity, can be considered a diagnostic marker of ccRCCs. Furthermore, as many reports exist relating CA IX inhibition to a better outcome to anticancer therapy in ccRCC, plasma levels of CA IX could be also predictive for response to therapy.
2017
33
234
240
Goal 3: Good health and well-being for people
Lucarini, Laura; Magnelli, Lucia; Schiavone, Nicola; Crisci, Alfonso; Innocenti, Alessio; Puccetti, Luca; Cianchi, Fabio; Peri, Sara; Supuran, CLAUDIU...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1104503
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