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Evaluation of the anticancer effects exerted by 5-fluorouracil and heme oxygenase-1 inhibitor hybrids in HTC116 colorectal cancer cells.
Salerno, Loredana; Notaro, Antonietta; Consoli, Valeria; Affranchi, Federica; Pittalà, Valeria; Sorrenti, Valeria; Vanella, Luca; Giuliano, Michela; Intagliata, Sebastiano.
Affiliation
  • Salerno L; Department of Drug and Health Sciences, University of Catania, Catania, Italy.
  • Notaro A; Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Palermo, Italy.
  • Consoli V; Department of Drug and Health Sciences, University of Catania, Catania, Italy.
  • Affranchi F; Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Palermo, Italy.
  • Pittalà V; Department of Drug and Health Sciences, University of Catania, Catania, Italy.
  • Sorrenti V; Department of Molecular Medicine, Arabian Gulf University, Manama, Bahrain.
  • Vanella L; Department of Drug and Health Sciences, University of Catania, Catania, Italy.
  • Giuliano M; Department of Drug and Health Sciences, University of Catania, Catania, Italy.
  • Intagliata S; Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Palermo, Italy.
J Enzyme Inhib Med Chem ; 39(1): 2337191, 2024 Dec.
Article in En | MEDLINE | ID: mdl-38634597
ABSTRACT
Colon cancer remains a clinical challenge in industrialised countries. Its treatment with 5-Flurouracil (5-FU) develops many side effects and resistance. Thus, several strategies have been undertaken so far, including the use of drug cocktails and polypharmacology. Heme oxygenase-1 (HO-1) is an emerging molecular target in the treatment of various cancers. We recently demonstrated that a combination of HO-1 inhibitors with 5-FU and the corresponding hybrids SI1/17, SI1/20, and SI1/22, possessed anticancer activity against prostate and lung cancer cells. In this work, we evaluated these hybrids in a model of colon cancer and found that SI1/22 and the respective combo have greater potency than 5-FU. Particularly, compounds inhibit HO-1 activity in cell lysates, increase ROS and the expression of HO-1, SOD, and Nrf2. Moreover, we observed a decrease of pro-caspase and an increase in cleaved PARP-1 and p62, suggesting apoptotic and autophagic cell death and potential application of these drugs as anticancer agents.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colonic Neoplasms / Fluorouracil / Antineoplastic Agents Limits: Humans / Male Language: En Journal: J Enzyme Inhib Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colonic Neoplasms / Fluorouracil / Antineoplastic Agents Limits: Humans / Male Language: En Journal: J Enzyme Inhib Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Document type: Article Affiliation country: Italy