Abstract

BackgroundTaxol is an effective antineoplastic agent, originally extracted from the bark of Taxus brevifolia with a low yield. Many attempts have been made to produce Taxol by chemical synthesis, semi-synthesis and plant tissue cultures. However, to date, the availability of this compound is not sufficient to satisfy the commercial requirements. The aim of the present work was to produce suspension cell cultures from plants not belonging to Taxus genus and to verify whether they produced Taxol and taxanes. For this purpose different explants of hazel (Corylus avellana species) were used to optimize the protocol for inducing in vitro callus, an undifferentiated tissue from which suspension cell cultures were established.ResultsCalli were successfully induced from stems, leaves and seeds grown in various hormone concentrations and combinations. The most suitable callus to establish suspension cell cultures was obtained from seeds. Media recovered from suspension cell cultures contained taxanes, and showed antiproliferative activity on human tumour cells. Taxol, 10-deacetyltaxol and 10-deacetylbaccatin III were the main taxanes identified. The level of Taxol recovered from the media of hazel cultures was similar to that found in yew cultures. Moreover, the production of taxanes in hazel cell cultures increased when elicitors were used.ConclusionHere we show that hazel cell cultures produce Taxol and taxanes under controlled conditions. This result suggests that hazel possesses the enzymes for Taxol production, which until now was considered to be a pathway particular to Taxus genus. The main benefit of producing taxanes through hazel cell cultures is that hazel is widely available, grows at a much faster rate in vivo, and is easier to cultivate in vitro than yew. In addition, the production of callus directly from hazel seeds shortens the culture time and minimizes the probability of contamination. Therefore, hazel could become a commercial source of Taxol and taxanes, both to be used as new therapeutic agents or as new precursors for Taxol semi-synthesis.

Highlights

  • Taxol is an effective antineoplastic agent, originally extracted from the bark of Taxus brevifolia with a low yield

  • Here we show that hazel cell cultures produce Taxol and taxanes under controlled conditions

  • This result suggests that hazel possesses the enzymes for Taxol production, which until now was considered to be a pathway particular to Taxus genus

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Summary

Introduction

Taxol is an effective antineoplastic agent, originally extracted from the bark of Taxus brevifolia with a low yield. The aim of the present work was to produce suspension cell cultures from plants not belonging to Taxus genus and to verify whether they produced Taxol and taxanes. The major limitation encountered in the extensive use of this drug is its short supply, since T. brevifolia, as well as other Taxus spp, yields very low amounts of Taxol. Extraction of this compound from the intact plant generally requires labour intensive procedures, besides posing environmental concerns. Most of the drug for clinical use is produced by semi-synthesis [8], starting from a natural precursor, 10-deacetylbaccatin III, which can be obtained from differentiated yew tissues, mainly leaves, with a relatively good yield [9,10]. The semi-synthetic approach suffers from some limitations, relied upon the extraction and isolation of the precursor from differentiated tissues, which can vary significantly in yield, depending on epigenetic and environmental factors [11,12]

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