Abstract

Colorectal cancer is the third most common diagnosed cancer globally. Although substantial advances have been obtained both in treatment and survival rates, there is still a need for new therapeutical approaches. Natural compounds are a realistic source of new bioactive compounds with anticancer activity. Among them, rosemary polyphenols have shown a vast antiproliferative capacity against colon cancer cells in vitro and in animal models. We have investigated the antitumor activity of a rosemary extract (RE) obtained by using supercritical fluid extraction through its capacity to inhibit various signatures of cancer progression and metastasis such as proliferation, migration, invasion and clonogenic survival. RE strongly inhibited proliferation, migration and colony formation of colon cancer cells regardless their phenotype. Treatment with RE led to a sharp increase of intracellular ROS that resulted in necrosis cell death. Nrf2 gene silencing increased RE cytotoxic effects, thus suggesting that this pathway was involved in cell survival. These in vitro results were in line with a reduction of tumor growth by oral administration of RE in a xenograft model of colon cancer cells using athymic nude mice. These findings indicate that targeting colon cancer cells by increasing intracellular ROS and decreasing cell survival mechanisms may suppose a therapeutic option in colon cancer through the combination of rosemary compounds and chemotherapeutic drugs.

Highlights

  • Colorectal cancer (CRC) is the second most commonly diagnosed cancer type in females and the third in males globally, with increasing prevalence even in traditionally low-risk countries

  • The results show a dose-dependent antiproliferative effect (Supplementary Fig. 1) and that the triterpenes ursolic acid (UA) and betulinic acid (BA) exhibited higher antiproliferative effect than the diterpenes carnosic acid (CA) and CAR and all isolated compounds tested showed lower IC50 values than rosemary extract (RE) extract

  • Our previous research characterized in detail by HPLC-ESI-QTOF-MS the composition of the RE utilized in the present work, showing that diterpenes (CA and CAR) and triterpenes (UA and BA) were the most abundant compounds[13]

Read more

Summary

Introduction

Colorectal cancer (CRC) is the second most commonly diagnosed cancer type in females and the third in males globally, with increasing prevalence even in traditionally low-risk countries. Several dietary components found in plant-derived foods, medicinal plants as well as their bioactive compounds have shown protective effects against a wide range of cancers, including colon cancer[2,3,4]. The antiproliferative effect of a terpenes-enriched rosemary extract (RE) obtained using supercritical fluid extraction has been demonstrated in colon cancer cell models[13]. CAR might be the main compounds responsible for such effects, but the higher activity of the complete extract compared to the fractions suggested the potential synergistic interaction between diterpenes and triterpenes. The potential molecular mechanism of this antiproliferative effect and the pharmacological interactions between RE components are still unknown. The mechanism of the antiproliferative activity has been fully characterized by proliferation, migration, invasion and cell cycle assays in three different colon cancer cell lines. We assessed the effect of RE on tumor progression in vivo in colon cancer mouse xenografts

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call