Your browser doesn't support javascript.
loading
Next generation sequencing and functional pathway analysis to understand the mechanism of action of copper-tolfenamic acid against pancreatic cancer cells.
Hurtado, Myrna; Prokai, Laszlo; Sankpal, Umesh T; Levesque, Blair; Maram, Rajasekhar; Chhabra, Jaya; Brown, Deondra T; Gurung, Raj K; Holder, Alvin A; Vishwanatha, Jamboor K; Basha, Riyaz.
Afiliación
  • Hurtado M; Biochemistry and Cancer Biology, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
  • Prokai L; Department of Pharmacology and Neuroscience, Institute for Healthy Aging, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
  • Sankpal UT; Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
  • Levesque B; Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
  • Maram R; Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
  • Chhabra J; Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA, 23529, United States.
  • Brown DT; Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA, 23529, United States.
  • Gurung RK; Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA, 23529, United States.
  • Holder AA; Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA, 23529, United States.
  • Vishwanatha JK; Department of Microbiology, Immunology and Genetics, Graduate School of Biomedical Sciences University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
  • Basha R; Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX, 76107, United States.
Process Biochem ; 89: 155-164, 2020 Feb.
Article en En | MEDLINE | ID: mdl-32719579
Anti-cancer activity of tolfenamic acid (TA) in preclinical models for pancreatic cancer (PaCa) is well established. Since the dosage for anti-cancer actions of TA is rather high, we recently demonstrated that IC50 values of Copper-TA are 30-80% less than TA in 12 cancer cell lines. This study elucidates the underlying mechanisms of Copper-TA in PaCa cells. Control and Copper-TA (IC50) treated PaCa cells were processed by next-generation sequencing (NGS) to determine differentially expressed genes using HTG EdgeSeq Oncology Biomarker panel. Ingenuity Pathway Analysis (IPA®) was used to identify functional significance of altered genes. The conformational studies for assessing the expression of key regulators and genes were conducted by Western blot and qPCR. IPA® identified several networks, regulators, as well as molecular and cellular functions associated with cancer. The top 5 molecular and cellular functions affected by Cu-TA treatment were cell death and survival, cellular development, cell growth and proliferation, cell cycle and cellular movement. The expression of top upstream regulators was confirmed by Western blot analysis while qPCR results of selected genes demonstrated that Copper-TA is efficacious at lower doses than TA. Results suggest that Copper-TA alters genes/key regulators associated with cancer and potentially serve as an effective anti-cancer agent.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Process Biochem Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Process Biochem Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido