比较比较有意思课题组的研究思路
CHEMISTRY OF BIOACTIVE NATURAL PRODUCTS
Corrado Tringali (Full Professor)
Vincenzo Amico (Full Professor)
Rosa Chillemi (Assistant Professor)
Sebastiano Sciuto (Associate Professor)
Carmela Spatafora (Assistant Professor)
Valentina Greco (PhD student)
Vedamurthy Bhusainahally M. (PhD st.)
Our Chemistry is close to Nature: we study bioactive natural products and in recent years our group has devoted the main part of its research activity to the synthesis of analogues of
biomolecules, in particular polyphenols (Figure 1) and nucleic acids. We carry out
‘biomimetic’ reactions, working also with enzymes, to obtaining compounds potentially useful as anticancer drugs. We are also working on projects for a sustainable development, studying the exploitation of agro-industrial biomasses (such as almond crop, wine-making and biofuels waste by-products) to obtain useful products, to be employed as antioxidant
for food or cosmetic applications or as adjuvants for pharmaceutical use.
Keywords: natural products; polyphenols; biomasses; synthesis; oligonucleotides.
1. Synthesis of analogues of natural products as potential antitumor agents.
The attention to natural products as ‘lead compounds’ in drug discovery has been renewed recently. In particular, an authoritative report on Journal of Natural Products has highlighted that the majority of the currently employed antitumor drugs is of natural origin, or has been obtained through modification of a natural precursor, or has to be considered ‘mimetic’ of natural products on the basis of its mechanism of action (D.J. Newman and G. M. Cragg, J. Nat. Prod. 70, 462-477, 2007). In addition, it has been observed that many polyphenols, frequently present in foods or beverages, show cancer chemopreventive properties, associated with low or absent citotoxicity, and may be useful ‘adjuvants’ in cancer therapy. For these reasons, our group in recent years has devoted the Endothelial Growth Factor) is a new tool in cancer chemotherapy: without new blood vessels, in fact, a carcinoma cannot grow beyond a very small size, nor can it metastasise to distant organs. We have focused our attention on the optimization of the properties of selected natural polyphenols; in fact, many antitumor diet polyphenols, such as the well known stilbenoid resveratrol , found in grape and red wine (see Figure 1), have a low bioavailability, being easily converted to metabolic intermediates. Thus, employing chemical and enzymatic methods, we have recently synthesized a number of resveratrol analogues (including E and Z isomers) some of them showing optimized metabolic stability and higher antiproliferative activity than the natural model; among these, Z -3,5,4’-
trimethoxystilbene showed potent antiproliferative activity against DU-145, LNCaP (prostate), KB (mouth epidermoic) and SW480 (colon) cancer cells; other
cis methoxylated stilbenoids proved to be potently active against SW480 cells and a docking study revealed their binding affinity with the colchicine site of tubulin in analogy with combretastatin A. Interestingly, the E -2-hydroxy-3,5,4’-Further studies on methylated/acetylated resveratrol analogues showed that other synthetic preparation of hydrosoluble resveratrol analogues, and the 3-O -phosphorylresveratrol, a potential prodrug of the natural stilbenoid, resulted more active than resveratrol itself against DU-145 cells, O -phosphorylresveratrol. Our current synthetic projects on resveratrol derivatives are addressed to two different targets: a) conjugated resveratrol analogues, incorporating a colesteryl pendant, to be synthesized through phopsphoramidites
intermediates; b) analogues of viniferins, a
group of natural stilbenoid dimers with antitumor
properties, to be obtained through enzymatic
oxidative coupling of stilbenoid monomers.
In current literature, the term ‘lignans ’ is
commonly employed to indicate a large family of
widespread natural products, biosynthetically
originated by oxidative coupling of two
phenylpropanoid (C6C 3) units, which display an
impressive structural diversity and a comparable
variety of biological activities. In particular, some
neolignans have been reported as antimitotic,
antiangiogenic and pro-apoptotic agents. Thus,
lignans and related compounds are an attractive
target for chemical synthesis or modification. We
employed biomimetic dimerization reactions
carried out through a radical phenolic oxidative
coupling of natural precursors, to obtain ‘unnatural’ products by a mechanism mimicking the ‘natural’ esters, namely CAPE (Caffeic Acid Phenethyl Ester, a well-known component of propolis, see methyl caffeate. The reaction afforded with good yields (72% for CAPE dimerization) unusual, fluorescent benzo[kl ]xanthene lignans (see Figure 2) as main products.
We carried out also a mechanistic study of this oxidative coupling reactions, and applied this
methodology to synthesize the
natural benzoxanthene lignans
Benzo[kl]xanthene lignans are very
rare both among natural products
and synthetic analogues and
consequently are almost
unexplored with regard to their
biological properties and possible
pharmacological applications. Thus,
and molecular docking, paralleled
by evaluation of their
480 (colon carcinoma) and HepG2 (hepatoblastoma) cancer cell lines. A small panel of compounds
was used to obtain preliminary SAR data. The results reveal that the planar chromophoric moiety of the benzoxanthene lignans is intercalated between two DNA base pairs and the flexible appendages are collocated along the grooves of nucleic acid and make contacts with the external
bulky phenylethyl groups, giving wider Van der Waals contacts with the minor groove, improve the binding affinity, as highlighted by the higher calculated inhibition constants and the higher observed solid hypoxic tumors, which are more resistant to radiation and chemotherapeutic drugs than their normoxic counterparts. Further natural-derived compounds related to polyphenols will be synthesized in the next future, and their antiproliferative activity, vascularisation inhibitory properties and interaction with DNA will be evaluated.
2. Synthesis of oligonucleotides conjugated to natural lipids
Great interest is found in the literature
regarding to the synthesis of oligonucleotides
conjugated to various lipophilic moieties. But,
until a few years ago, it was not possible to
prepare phosphatidyloligonucleotides owing to
an actual difficulty encountered in a direct
attachment of the phosphatidyl group to
oligonucleotides elongated on the solid phase
by standard phosphoramidite chemistry
procedures. Some current synthetic
opportunities, available for the preparation of
oligonucleotides bearing residual base-labile
side groups, has allowed us recently to design
a synthetic path for obtaining 5’-O -phosphatidyloligonucleotides . So, by applying this synthetic different fatty acids; stearoyl, palmitoyl and myristoyl residues being employed for this purpose. The spectral properties and the ability of these phosphatidyloligonucleotides to interact with lipid monolayers to give stable duplexes with the target sequence have been studied. Further evaluation of biological activity of the newly synthesized phosphatidyl antisense molecules is in progress.
2. Agro-industrial biomasses as a source of antioxidative and antitumor agents
Agro-industrial biomasses are a source of potential antitumor compounds; in fact, these materials relationship between antioxidant and pro-apoptotic activity these components may be useful also as adjuvants for cancer therapy. We have recently identified by HPLC-UV-MS and/or chromatographic by-products; in particular from grape pomace we obtained antioxidative fractions, whereas
bioguided chromatographic isolation from grape stems afforded
antiproliferative constituents, among them resveratrol ; from
almond hulls we obtained a number of bioactive constituents and in
particular betulinic acid showed potent MCF-7 cell growth
inhibitory activity. This methodology will be applied to further
biomasses from or carrying out studies on oilseed cakes (Figure 5) from biofuel
production ( spp. andwork is to obtain further polyphenol-enriched fractions or pure
compounds with antioxidant, pro-apoptotic or antiproliferative
properties to be optimized as anticancer adjuvants.
Collaborations and Research Grants
• Prof. Dale G. Nagle – Mississippi University - USA
• Dr. Valery Morris - Queensborough Community College – New York City - USA
• Prof. Olle Soder – Karolinska Institutet – Stoccolma - Svezia
• Prof. Attilio Di Pietro – Université de Lyon – Lione – Francia
• Prof. Norbert Latruffe – Université de Bourgogne – Digione – Francia
• Dr. Lin Haishu- National University of Singapore - Singapore
• Dr. Gopala Srinivas – S. C. T. Institute for Medical Science and Technology - Kerala – India • Prof.ssa Giuseppina Basini – Università di Parma
• Proff. Giuseppe Bifulco e Raffaele Riccio – Università di Salerno
Grants: PRIN 2007; PRA 2008; BIONAP srl
Selected Publications
S. DI MICCO, C. DAQUINO, C. SPATAFORA, F. MAZUÉ, D. DELMAS, N. LATRUFFE, TRINGALI C., R. RICCIO, G. BIFULCO (2010). Structural basis for the potential antitumour activity of DNA-interacting Benzo[kl ]xanthene lignans. ORGANIC & BIOMOLECULAR CHEMISTRY, in press
F. MAZUÉ, D. COLIN, J. GOBBO, M. WEGNER, A. RESCIFINA, C. SPATAFORA, D. FASSEUR, D. DELMAS, P. MEUNIER, TRINGALI C., N. LATRUFFE (2010). Structural determinants of resveratrol for cell proliferation inhibition potency: experimental and docking studies of new analogs. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, vol. 45; p. 2972-2980.
G. BASINI, TRINGALI C., L. BAIONI, S. BUSSOLATI, C. SPATAFORA, F. GRASSELLI (2010). Biological effects on granulosa cells of hydroxylated and methylated resveratrol analogues. MOLECULAR NUTRITION & FOOD RESEARCH, vol 54; p 236-243.
R. CHILLEMI, S. SCIUTO, C. SPATAFORA, TRINGALI C. (2010). Hydroxytyrosol lipophilic analogues: synthesis, radical scavenging activity and human cell oxidative damage protection. In: VICTOR R. PREEDY AND RONALD ROSS WATSON EDS. OLIVES AND OLIVE OIL IN HEALTH AND DISEASE PREVENTION. p. 1233-1243, OXFORD: Academic press
C. DAQUINO, A. RESCIFINA, C. SPATAFORA, TRINGALI C. (2009). Biomimetic synthesis of natural and ‘unnatural’ lignans and neolignans by oxidative coupling of caffeic esters. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, p. 6289-6300.
C. SPATAFORA, G. BASINI, L. BAIONI, F. GRASSELLI, A. SOFIA, TRINGALI C. (2009). Antiangiogenic Resveratrol Analogues by Mild m-CPBA Aromatic Hydroxylation of 3,5-Dimethoxystilbenes. NATURAL PRODUCT COMMUNICATIONS, vol. 4; p. 239-246
K. SVECHNIKOV, C. SPATAFORA, I. SVECHNIKOVA, TRINGALI C., O. SÖDER (2009). Effects of resveratrol analogues on steroidogenesis and mitochondrial function in rat Leydig cells in vitro. JOURNAL OF APPLIED TOXICOLOGY, vol. 29; p. 673-680.
V. AMICO, V. BARRESI, R. CHILLEMI, D. F. CONDORELLI, S. SCIUTO, C. SPATAFORA, TRINGALI C. (2009). Bioassay-Guided Isolation of Antiproliferative Compounds from Grape (Vitis vinifera) Stems. NATURAL PRODUCT COMMUNICATIONS, vol. 4; p. 27-34.
V. AMICO, R. CHILLEMI, S. MANGIAFICO, C. SPATAFORA, TRINGALI C. (2008). Polyphenol-enriched fractions from Sicilian grape pomace: HPLC-DAD analysis and antioxidant activity. BIORESOURCE TECHNOLOGY, vol. 99; p. 5960-5966
D. ALEO, V. CARDILE, R. CHILLEMI, G. GRANATA, S. SCIUTO, (2008). Chemoenzymatic synthesis and some biological properties of O -phosphoryl derivatives of (E )-resveratrol. NATURAL PRODUCT COMMUNICATIONS, vol.3, p. 1693-1700.
R. CHILLEMI, S. SCIUTO, C. SPATAFORA, TRINGALI C. (2007). Anti-tumor properties of stilbene-based resveratrol analogues: recent results. NATURAL PRODUCT COMMUNICATIONS, vol. 2; p. 499-513.
S. GRASSO, L. SIRACUSA, C. SPATAFORA, M. RENIS, TRINGALI C. (2007). Hydroxytyrosol lipophylic analogues: enzymatic synthesis, radical scavenging activity and DNA damage protection. BIOORGANIC CHEMISTRY, vol. 35; p. 137-152.
V. AMICO, V. BARRESI, D. F. CONDORELLI, C. SPATAFORA, TRINGALI C. (2006). Antiproliferative terpenoids from almond hulls (Prunus dulcis): identification and structure-activity relationships. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, vol. 54; p. 810-814.
R. CHILLEMI, D. ALEO, G. GRANATA, S. SCIUTO (2006) Synthesis of Very Short Chain Lysophosphatidyl-oligodeoxyribonucleotides. BIOCONJUGATE CHEMISTRY , vol 17, p. 1022-1029.