Journal Article

Effects of ATRA combined with citrus and ginger-derived compounds in human SCC xenografts

Remeika, Angela, Mathis, J Michael, Adegboyega, Patrick, Kleiner-Hancock, Heather E, Gill, Jennifer N, Clifford, John L, Syed, Zanobia, Shi, Runhua, Prince, Misty, Robbins, Delira

2010

Overview

Background NF-κB is a survival signaling transcription factor complex involved in the malignant phenotype of many cancers, including squamous cell carcinomas (SCC). The citrus coumarin, auraptene (AUR), and the ethno-medicinal ginger (Alpinia galanga) phenylpropanoid, 1'-acetoxychavicol acetate (ACA), were previously shown to suppress 12- O -tetradecanoylphorbol-13-acetate (TPA) induced mouse skin tumor promotion. The goal of the present study was to determine whether AUR and ACA are effective either alone or in combination with all- trans retinoic acid (ATRA) for suppressing SCC tumor growth. Methods We first determined the effects of orally administered ACA (100 mg/kg bw) and AUR (200 mg/kg bw) on lipopolysaccharide (LPS)-induced NF-κB activation in NF-κB-RE-luc (Oslo) luciferase reporter mice. Dietary administration of AUR and ACA ± ATRA was next evaluated in a xenograft mouse model. Female SCID/bg mice were fed diets containing the experimental compounds, injected with 1 × 10 6 SRB12-p9 cells s.c., palpated and weighed twice a week for 28 days following injection. Results Both ACA and AUR suppressed LPS-induced NF-κB activation in the report mice. In the xenograft model, AUR (1000 ppm) and ACA (500 ppm) modestly suppressed tumor volume. However, in combination with ATRA at 5, 10, and 30 ppm, ACA 500 ppm significantly inhibited tumor volume by 56%, 62%, and 98%, respectively. The effect of ATRA alone was 37%, 33%, and 93% inhibition, respectively. AUR 1000 ppm and ATRA 10 ppm were not very effective when administered alone, but when combined, strongly suppressed tumor volume by 84%. Conclusions Citrus AUR may synergize the tumor suppressive effects of ATRA, while ACA may prolong the inhibitory effects of ATRA. Further studies will be necessary to determine whether these combinations may be useful in the control of human SCC.

• Publisher: BioMed Central,BioMed Central Ltd,BMC
• Subject: Animals / Antineoplastic Agents - pharmacology / Benzyl Alcohols - pharmacology / Biomedical and Life Sciences / Biomedicine / Blotting, Western / Cancer Research / Carcinoma, Squamous Cell - drug therapy / Carcinoma, Squamous Cell - metabolism / Carcinoma, Squamous Cell - pathology / Citrus - drug effects / Clinical oncology / Coumarins - pharmacology / Drug Synergism / Drug Therapy, Combination / Female / Genetic aspects / Health Promotion and Disease Prevention / Humans / Lipopolysaccharides - pharmacology / Luciferases - metabolism / Male / Medicine/Public Health / Mice / Mice, SCID / NF-kappa B - genetics / NF-kappa B - metabolism / Oncology / Physiological aspects / Plant Extracts - pharmacology / Research Article / Risk factors / Skin cancer / Skin Neoplasms - drug therapy / Skin Neoplasms - metabolism / Skin Neoplasms - pathology / Squamous cell carcinoma / Surgical Oncology / Transcription factors / Tretinoin - pharmacology / Tumor Cells, Cultured / Xenograft Model Antitumor Assays / Zingiber officinale - drug effects