Planta Med 2007; 73(1): 49-52
DOI: 10.1055/s-2006-951767
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Identification of a New Natural Camptothecin Analogue in Targeted Screening for HIF-1α Inhibitors

Paul Klausmeyer1 , Thomas G. McCloud1 , Giovanni Melillo2 , Dominic A. Scudiero3 , John H. Cardellina II4 , Robert H. Shoemaker4
  • 1Natural Products Support Group, SAIC-Frederick, Inc., NCI Frederick, Frederick, Maryland, USA
  • 2DTP Tumor Hypoxia Laboratory, SAIC-Frederick, Inc., NCI Frederick, Frederick, Maryland, USA
  • 3In Vitro Cell Line Screening Program, SAIC-Frederick, Inc., NCI Frederick, Frederick, Maryland, USA
  • 4Screening Technologies Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute FCRDC, Frederick, Maryland, USA
Further Information

Publication History

Received: August 30, 2006

Accepted: October 20, 2006

Publication Date:
21 December 2006 (online)

Abstract

Screening to detect compounds that inhibit the HIF-1α transcriptional activation pathway identified an extract of Ophiorrhiza trichocarpon for investigation. A high throughput dereplication strategy was employed, involving chromatography with spectral data acquisition supported by bioactivity testing and literature referencing, which led to rapid identification of camptothecin (1) and three analogues (2 - 4) as the active compounds. 9,10-Methylenedioxy-(20S)-camptothecin (4) was found for the first time from a plant.

References

  • 1 Semenza G L. Targeting HIF-1 for cancer therapy.  Nat Rev Cancer. 2003;  3 721-32
  • 2 Belozerov V E, Van Meir E G. Hypoxia inducible factor-1: a novel target for cancer therapy.  Anticancer Drugs. 2005;  16 901-9
  • 3 Rapisarda A, Uranchimeg B, Scudiero D A, Selby M, Sausville E A, Shoemaker R H. et al . Identification of small molecule inhibitors of hypoxia-inducible factor 1 transcriptional activation pathway.  Cancer Res. 2002;  62 4316-24
  • 4 Kong D, Park E J, Stephen A G, Calvani M, Cardellina JH I I, Monks A. et al . Echinomycin, a small-molecule inhibitor of hypoxia-inducible factor-1 DNA-binding activity.  Cancer Res. 2005;  65 9047-55
  • 5 Creighton-Gutteridge M, Cardellina JH I I, Stephen A G, Rapisarda A, Uranchimeg B, Hite K. et al .As of 10 DEC 2006. Cancer Res, in press
  • 6 Tan C, de Noronha R G, Roecker A J, Pyrzynska B, Khwaja F, Zhang Z. et al . Identification of a novel small-molecule inhibitor of the hypoxia-inducible factor 1 pathway.  Cancer Res. 2005;  65 605-12
  • 7 Hodges T W, Hossain C F, Kim Y -P, Zhou Y -D, Nagle D G. The Saururus cernuus dineolignans manassantin B and 4-O-demethylmanassantin B are potent inhibitors of hypoxia-activated HIF-1.  J Nat Prod. 2004;  67 767-71
  • 8 Lin S, Tsai S -C, Lee C -C, Wang B -W, Liou J -Y, Shyu K -G. Berberine inhibitis HIF-1α expression via enhanced proteolysis.  Mol Pharmacol. 2004;  66 612-9
  • 9 Li M -H, Miao Z -H, Tan W -F, Yue J -M, Zhang C, Lin L -P. et al . Pseudolaric acid B inhibitis angiogenesis and reduces hypoxia-inducible factor 1α by promoting proteasome-mediated degradation.  Clin Cancer Res. 2004;  10 8266-74
  • 10 Mohammed K A, Hossain C F, Zhang L, Bruick R K, Zhou Y -D, Nagle D G. Laurenditerpenol, a new diterpene from the tropical marine alga Laurencia intricata that potently inhibits HIF-1 mediated hypoxic signaling in breast tumor cells.  J Nat Prod. 2004;  67 2002-7
  • 11 Rapisarda A, Uranchimeg B, Sordet O, Pommier Y, Shoemaker R H, Melillo G. Topoisomerase I-mediated inhibition of hypoxia-inducible factor 1: mechanism and therapeutic implications.  Cancer Res. 2004;  64 1475-82
  • 12 Schanzer I. Systematic notes on Ophiorrhiza trichocarpon Blume (Rubiaceae) and some related species.  Thai For Bull (Bot). 2004;  32 132-45
  • 13 Klausmeyer P, Chmurny G N, McCloud T G, Tucker K D, Shoemaker R H. A novel antimicrobial indolizinium alkaloid from Aniba panurensis .  J Nat Prod. 2004;  67 1732-5
  • 14 Klausmeyer P, McCloud T G, Tucker K D, Cardellina JH I I, Shoemaker R H. Aspirochlorine class compounds from Aspergillus flavus inhibit azole-resistant Candida albicans .  J Nat Prod. 2005;  68 1300-2
  • 15 Meragelman T L, Cardellina JH I I, McCloud T G, Shoemaker R H. Antifungal flavonoids from Hildegardia barteri .  J Nat Prod. 2005;  68 1790-2
  • 16 Lin L -Z, Cordell G A. 13C-NMR assignments of camptothecine and 10-hydroxycamptothecine.  J Nat Prod. 1990;  53 186-9
  • 17 Wall M E, Wani M C, Cook C E, Palmer K H, McPhail A T, Sim G A. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata .  J Am Chem Soc. 1966;  88 3888-90
  • 18 Aimi N, Nishimura M, Miwa A, Hoshino H, Sakai S -I, Haginiwa J. Pumiloside and deoxypumiloside; plausible intermediates of camptothecin biosynthesis.  Tetrahedron Lett. 1989;  30 4991-4
  • 19 Tafur S, Nelson J D, DeLong D C, Svoboda G H. Antiviral components of Ophiorrhiza mungos. Isolation of camptothecin and 10-methoxycamptothecin.  J Nat Prod. 1976;  39 261-2
  • 20 Roja G. Comparative studies on the camptothecin content from Nothapodytes foetida and Ophiorrhiza species.  Nat Prod Res. 2005;  20 85-8
  • 21 Saito K, Sudo H, Yamazaki M, Koseki-Nakamura M, Kitajima M, Takayama H. et al . Feasible production of camptothecin by hairy root culture of Ophiorrhiza pumila .  Plant Cell Rep. 2001;  20 267-71
  • 22 Yamazaki Y, Urano A, Sudo H, Kitajima M, Takayama H, Yamazaki M. et al . Metabolite profiling of alkaloids and strictosidine synthase activity in camptothecin producing plants.  Phytochemistry. 2003;  62 461-70
  • 23 Kitajima M, Fujii N, Yoshino F, Sudo H, Saito K, Aimi N. et al . Camptothecins and two new monoterpene glucosides from Ophiorrhiza liukiuensis .  Chem Pharm Bull. 2005;  53 1355-8
  • 24 Aimi N, Tsuyuki T, Murakami H, Sakai S, Haginiwa J. Isolation and partial synthesis of 3(R)- and 3(S)-deoxypumiloside; structural revision of the key metabolite from the camptothecin producing plant, Ophiorrhiza pumila .  Tetrahedron Lett. 1996;  38 4255-8
  • 25 Govindachari T R, Viswanathan N. Alkaloids of Mappia foetida .  Phytochemistry. 1972;  11 3529-31
  • 26 Roja G, Heble M R. The quinoline alkaloids camptothecin and 9-methoxycamptothecin from tissue cultures and mature trees of Nothapodytes foetida .  Phytochemistry. 1994;  36 65-6
  • 27 Zhou B -N, Hoch J M, Johnson R K, Mattern M R, Eng W -K, Ma J. et al . Use of COMPARE analysis to discover new natural product drugs: Isolation of camptothecin and 9-methoxycamptothecin from a new source.  J Nat Prod. 2000;  63 1273-6
  • 28 Puri S C, Verma V, Amna T, Qazi G N, Spiteller M J. An endophytic fungus from Nothapodytes foetida that produces camptothecin.  J Nat Prod. 2005;  68 1717-9
  • 29 Wall M E, Wani M C, Nicholas A W, Manikumar G, Tele C, Moore L. et al . Synthesis and structure activity of novel camptothecin analogs.  J Med Chem. 1993;  36 2689-700

Thomas G. McCloud

Natural Products Support Group

SAIC-Frederick, Inc.

NCI Frederick

Frederick

Maryland, 21702-1201

USA

Phone: +1-301-846-5750

Fax: +1-301-846-5206

Email: mccloud@dtpax2.ncifcrf.gov

>