Elucidation of underlying molecular mechanism of 5-Fluorouracil chemoresistance and its restoration using fish oil in experimental colon carcinoma

Mol Cell Biochem. 2021 Mar;476(3):1517-1527. doi: 10.1007/s11010-020-03999-x. Epub 2021 Jan 4.

Abstract

Latest strategies for cancer treatment primarily focus on the use of chemosensitizers to enhance therapeutic outcome. N-3 PUFAs have emerged as the strongest candidate for the prevention of colorectal cancer (CRC). Our previous studies have demonstrated that fish oil (FO) rich in n-3 PUFAs not only increased therapeutic potential of 5-Fluorouracil(5-FU) in colon cancer but also ameliorated its toxicity. Henceforth, the present study is designed to elucidate mechanistic insights of FO as a chemosensitizer to circumvent drug resistance in experimental colon carcinoma. The colon cancer was induced by 1,2-dimethylhydrazine(DMH)/dextran sulfate sodium(DSS) in male Balb/c mice and these animals were treated with 5-FU(12.5 mg/kg b.w.), FO(0.2 ml), or 5-FU + FO(12.5 mg/kg b.w + 0.2 ml) orally for 14 days. The molecular mechanism of overcoming 5-FU resistance using FO in colon cancer was delineated by estimating expression of cancer stem cell markers using flowcytometric method and drug transporters by immunohistochemistry and immunoblotting. Additionally, distribution profile of 5-FU and its cytotoxic metabolite, 5-FdUMP at target(colon), and non-target sites (serum, kidney, liver, spleen) was assessed using high-performance liquid chromatography(HPLC) method. The observations revealed that expression of CSCs markers was remarkably reduced after using fish oil along with 5-FU in carcinogen-treated animals. Interestingly, the use of FO alongwith 5-FU also significantly declined the expression of drug transporters (ABCB1,ABCC5) and consequently resulted in an increased cellular uptake of 5-FU and its metabolite, 5-FdUMP at target site (colon). It could be possibly associated with change in permeability of cell membrane owing to the alteration in membrane fluidity. The present study revealed the mechanistic insights of FO as a MDR revertant which successfully restored 5-FU-mediated chemoresistance in experimental colon carcinoma.

Keywords: 5-Fluoro-2′-deoxyuridine 5′ monophosphate (5-FdUMP); 5-Fluorouracil (5-FU); ATP-binding cassette (ABC) transporters; Colorectal cancer (CRC); Fish oil (FO); Multi drug resistance (MDR).

MeSH terms

  • 1,2-Dimethylhydrazine
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Animals
  • Antimetabolites, Antineoplastic / pharmacology
  • Antineoplastic Agents / pharmacology*
  • Cell Membrane / metabolism
  • Colon / cytology
  • Colon / drug effects
  • Colonic Neoplasms / chemically induced
  • Colonic Neoplasms / drug therapy*
  • Dextran Sulfate
  • Drug Resistance, Neoplasm*
  • Fatty Acids, Omega-3 / metabolism*
  • Fish Oils / chemistry*
  • Fish Oils / therapeutic use*
  • Fluorouracil / pharmacology*
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Multidrug Resistance-Associated Proteins / metabolism
  • Neoplastic Stem Cells / cytology
  • Permeability

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Abcc5 protein, mouse
  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents
  • Fatty Acids, Omega-3
  • Fish Oils
  • Multidrug Resistance-Associated Proteins
  • Dextran Sulfate
  • 1,2-Dimethylhydrazine
  • Fluorouracil