Investigational agents to enhance the efficacy of chemotherapy or radiation Check for in pancreatic cancer

• Type of Material: Article
• Authors: Myrna Hurtado, University of North Texas; Umesh T. Sankpal, University of North Texas; Amalendu Ranjan, University of North Texas; Rajasekhar Maram, University of North Texas; Jamboor K. Vishwanatha, University of North Texas; Purnachandra Ganji, Emory University; Bassel El-Rayes, Emory University; Riyaz Basha, University of North Texas
• Language: English
• Date: 2018-06-01
• Publisher: ELSEVIER SCIENCE INC
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2018 Elsevier B.V.
• License: Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International
• Final Published Version (URL): http://dx.doi.org/10.1016/j.critrevonc.2018.03.016
• Title of Journal or Parent Work: CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
• Volume: 126
• Start Page: 201
• End Page: 207
• Keywords: DOWN-REGULATION; Chemotherapy; Radiation; Oncology; TOLFENAMIC ACID; STELLATE CELLS; SYNTHETIC CURCUMIN ANALOGS; TUMOR-GROWTH; METASTATIC BREAST-CANCER; Combination treatment; Life Sciences & Biomedicine; FACTOR-KAPPA-B; GEMCITABINE; DUCTAL ADENOCARCINOMA; Science & Technology; Hematology; ANTITUMOR-ACTIVITY; Pancreatic cancer
• Research Categories: Health Sciences, Oncology; Health Sciences, Radiology

Abstract

Pancreatic cancer (PC) continues to be a fatal malignancy. With standard treatments having modest impact, alternative courses of actions are being investigated such as enhancing the efficacy of standard treatment through sensitization of PC cells to chemotherapy or radiation. This review emphasizes investigational agents that increase the responses to chemotherapy or radiation in PC models. Our group has extensively investigated on Curcumin (Cur), analogs (EF31, UBS109, and L49H37), nanoparticles and a small molecule Tolfenamic acid (TA) for enhancing therapeutic efficacy in both in vitro and in vivo assays. Cur has a low level of toxicity and promising anti-cancer activity, however, its clinical development has been limited by low bioavailability. Cur analogs and nanoparticles were synthesized to improve Cur's efficacy and bioavailability. These compounds were found to be effective in enhancing the therapeutic effects of chemotherapy in pre-clinical models. Small molecules such as NSAIDs have also been tested for the anti-cancer activity and induction of response of chemotherapy and radiation. Interest in TA, a NSAID, has recently increased due to promising preclinical data demonstrating its anti-cancer properties with minimum toxicity. TA also synergistically increased the response of XRT in PC cells and in an orthotropic mouse model. With strong preclinical evidence, research aimed at developing less toxic therapies for PC using Cur analogues or TA is ready for translation into clinical testing.