4.6 Article

Syringic acid from Tamarix aucheriana possesses antimitogenic and chemo-sensitizing activities in human colorectal cancer cells

期刊

PHARMACEUTICAL BIOLOGY
卷 51, 期 9, 页码 1110-1124

出版社

TAYLOR & FRANCIS LTD
DOI: 10.3109/13880209.2013.781194

关键词

Antimitogenic; apoptosis; cell perturbation; chemosensitization; proteasome

资金

  1. Kuwait University [SL05-04]
  2. Science Analytical Facilities (SAF) [GS01/01, GS03/01, GS01/03]

向作者/读者索取更多资源

Context: For its variety of biological activities, Tamarix aucheriana (Decne.) Baum. (Tamaricaceae) has an extensive history as a traditional Arab medicine. Objectives: Antimitogenic and chemo-sensitizing activities of syringic acid (SA) were studied against human colorectal cancer. Materials and methods: Chromatographic and spectral data were used for the isolation and identification of SA. MTT, flow cytometry, in vitro invasion and angiogenesis assays, fluoremetry, ELISA and Real Time qPCR were used to test antimitogenic and chemo-sensitizing activities of SA, cell cycle, apoptosis, proteasome and NF kappa B-DNA-binding activities, cancer cell invasion and angiogenesis, and expression of cell cycle/apoptosis-related genes. Results: SA showed a time- and dose-dependent (IC50 = 0.95-1.2 mg mL(-1)) antimitogenic effect against cancer cells with little cytotoxicity on normal fibroblasts (<= 20%). SA-altered cell cycle (S/G2-M or G1/G2-M phases) in a time-dependent manner, induced apoptosis, inhibited DNA-binding activity of NF kappa B (p <= 0.0001), chymotrypsin-like/PGPH (peptidyl-glutamyl peptide-hydrolyzing) (p <= 0.0001) and the trypsin-like (p <= 0.002) activities of 26S proteasome and angiogenesis. SA also differentially sensitized cancer cells to standard chemotherapies with a marked increase in their sensitivity to camptothecin (500-fold), 5FU (20 000-fold), doxorubicin (210-fold), taxol (3134-fold), vinblastine (1000-fold), vincristine (130-fold) and amsacrine (107-fold) compared to standard drugs alone. Discussion: SA exerted its chemotherapeutic and chemo-sensitizing effects through an array of mechanisms including cell-cycle arrest, apoptosis induction, inhibition of cell proliferation, cell migration, angiogenesis, NF kappa B DNA-binding and proteasome activities. Conclusion: These results demonstrate the potential of SA as an antimitogenic and chemo-sensitizing agent for human colorectal cancer.

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