Opioid Tripeptides Hybridized with trans‐1‐Cinnamylpiperazine as Proliferation Inhibitors of Pancreatic Cancer Cells in Two‐ and Three‐Dimensional in vitro Models. (21st September 2017)

• Record Type: Journal Article
• Authors: Laskowska, Anna K.; Puszko, Anna K.; Sosnowski, Piotr; Różycki, Krzysztof; Kosson, Piotr; Matalińska, Joanna; Durlik, Marek; Misicka, Aleksandra
• Is Part Of: ChemMedChem. Volume 12:Number 19(2017)
• Page Start: 1637
• Page End: 1644
• Publication Date: 2017-09-21
• Subjects: anticancer drugs -- opioid receptors -- pancreatic cancer -- peptidomimetics -- spheroids; Pharmaceutical chemistry -- Periodicals; 615.19005
• DOI: 10.1002/cmdc.201700453
• Languages: English
• ISSNs: 1860-7179

Abstract

Abstract: According to the World Health Organization, the mortality rate among patients with pancreatic cancer will increase in the upcoming years. Gemcitabine is the first choice for treatment of pancreatic malignancy, but increasing resistance to this drug is decreasing its overall efficacy. Studies on new therapies that target metabolic pathways, growth factor inhibitors, and tumor stroma or tumor stem cells are currently underway in many research groups. Herein we report the bioactive properties (cytotoxicity and hemolytic activity) of synthetic peptidomimetics containing an opioid tripeptide fragment (Tyr‐R 1 ‐R 2 ‐; where R 1 isd ‐Ala ord ‐Thr, and R 2 is Phe or Trp) hybridized with trans ‐1‐cinnamylpiperazine. These compounds are stable in plasma up to 96 h and exhibit low hemotoxicity and good inhibitory effects on cancer cell growth in two‐ and three‐dimensional in vitro models of pancreatic cancer. Abstract : Multidimensional potency : Pancreatic cancer is a deadly disease resistant to most chemotherapeutics. We synthesized a series of peptidomimetics that are hybrids of opioid tripeptides and trans ‐1‐cinnamylpiperazine. These compounds showed good bioactivity against pancreatic cancer cells in in vitro models. They were especially efficient against spheroids obtained from isolated carcinoma cells. Moreover, these hybrids are stable in plasma up to four days and exhibit very low hemotoxicity.