4.7 Article

Inhibitory Effect of CAPE and Kaempferol in Colon Cancer Cell LinesPossible Implications in New Therapeutic Strategies

Journal

Publisher

MDPI
DOI: 10.3390/ijms20051199

Keywords

natural compounds; polyphenols; colon cancer; CAPE; Kaempferol; Morin

Funding

  1. Project PNCDI III [29PFE/18.10.2018]
  2. Competitivity Operational Program [35/01.09.2016, MySMIS 103375, 3860]
  3. Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania [193/2014]
  4. Non-invasive intelligent systems for colorectal cancer diagnosis and prognosis based on circulating microRNAs integrated in the clinical workflow-INTELCOR [PN-II-PT-PCCA-2013-4-1959]
  5. project MicroRNAs biomarkers of response to chemotherapy and overall survival in colon cancer-Terry Fox Foundation

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Background: Phytochemicals are natural compounds synthesized as secondary metabolites in plants and represent an important source of molecules with therapeutic applications. Attention is accorded to their potential in anti-cancer therapies as single agents or adjuvant treatment. Herby, we evaluated the in vitro effects of a panel of natural compounds with focus on caffeic acid phenethyl ester (CAPE) and Kaempferol for the treatment of human colon cancer. Methods: We exposed two human colon cancer cell lines, RKO and HCT-116, followed by functional examination of cell viability, cell proliferation and invasion, cell cycle, apoptosis, and autophagy. Modifications in gene expression were investigated through microarray and detection of existing mutations and finding of new ones was done with the help of Next Generation Sequencing (NGS). Results: Both CAPE and Kaempferol inhibit cell proliferation, motility and invasion, and stimulate apoptosis and autophagy, concomitant with modifications in coding and noncoding genes' expression. Moreover, there are pathogenic mutations that are no longer found upon treatment with CAPE and Kaempferol. Conclusions: Our findings indicate that CAPE and Kaempferol have the ability to negatively influence the development and advancement of colon cancer in vitro by specifically altering the cells at the molecular level; this activity can be exploited in possible adjuvant therapies once the optimal dose concentration with minimal side effects but with cancer inhibitory activity is set in vivo.

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