Antitumoral Macrolide Antibiotics from Streptomyces sp. Ba16

방선균에서 분리한 Macrolide 계 항암활성물질

  • Published : 1994.08.01

Abstract

Three more unusual macrolides in addition to concnamycin B were isolated from the mycelium of Streptomyces sp. strain Bal6. These four compounds showed a potent cytotoxity to hunian cancer cell lines, SNU-1 (stomach cancer cell line), SNU-354 (liver cancer cell line), MCF- 7 (breast cancer cell line) and KB-3-1 (oral epidermoid carcinoma cell line). Interestingly, these compounds confered slight differential cytotoxity on RHEK-1, a human epidermal keratinocyte cell line immotalized by AD12-SV40 hybrid virus and RHEK-1/pSV$_{2}$ ras which was resulted from H-ras transfomation of RHEK-1. These compounds were determined to be concanamycin A, conca- namycin E and 0-methyl concanamycin B by NMR and other spectral analysis.

Keywords

References

  1. 한국산업미생물학회지 v.21 인체유방암세포주 MCF-7의 형태변화와 증식에 영향을 주는 항암활성물질, MCH-201 감항섭;김세은;김영호;이성우;오구택;김환묵;이정준
  2. Oncogene v.4 Neoplastic transformation of human ketatinocytes by polybrene-induced DNA-mediated transfer of an activated oncogene Rhim,J.S.;J.B.Park;G.Jay
  3. J. NCI. v.82 New calorimetric cytotoxicity assay for anticancer-drug screening Skehan,P.;R.Storeng;D.Scudiero;A.Monks;J.McMahon;D.Vistica;J.T.Warren;H.Bokesch;S.Kenny;M.R.Boyd
  4. Tetrahedron v.22 Structure of concanamycin A Kinashi,M.;K.Someno;K.Sakaguchi;T.Higashijima;T.Miyazawa
  5. J. Antibiotics v.37 Isolation and characterization of concanamycin A, B and C Kinash,H.;K.Someno;K.Sakaguchi
  6. J. Antibiotics v.37 The structure and absolute configuration of the 18-membered macrolide lactone antibiotic X-4357B(concanamycin A) Westley,J.W.;C.M.Liu;L.H.Sello;R.H.Evans;N.Troupe;J.F.Blount;A.M.Chiu;L.J.Todaro;P.A.Miller
  7. J. Antibiotics v.45 Isolation, characterization and biological activities of concanamycins as inhibitors of lysosomal acidification Woo,J.T.;C.Shinohara;K.Sakai;K.Hasumi;A.Endo
  8. J. Antibiotics v.45 Effects of prodigiosin 25-C on cultured cell lines: its similarity to monovalent polyether ionophores and vacuolar $H^ +$-ATPase inhibitors Kataoka,T.;J.Magae;K.Kasamo;H.Yamanishi;A.Endo;M.Yamasaki;K.Nagai
  9. J. Antibiotics v.43 Elevation of low density lipoprotein-receptor mRNA concentration in human hepatoma HepG2 cells by macrolide antibiotics Ogasawara,M.;N.Naruse;A.Yoshimura;Y.Hamagishi;T.Oki
  10. Cell v.65 Ras C-terminal processing enzymes-New drug target Gibbs,J.A.
  11. Molecular Carcinogenesis v.2 Permanent conversion of mouse and human cells transformed by activated ras or raf genes to apparently normal cells by treatment with the antibiotic azatyrosine Shindo-Okada,N.;O.Makabe;H.Nagahara;S.Nishimura
  12. Biochem. Biophys. Res. Commun. v.182 A noble compound, depudecin, induces production of transformation to the flat phenotype of NIH3T3 cells transformed by ras-oncogene Sugita,K.;H.Yoshida;M.Matsumoto;S.Matsutani
  13. TIBS v.18 Inhibitors of Ras farnesyltransferase Tamanoi,F.
  14. Science v.260 Selective inhibition of ras-depentent transformation by farnesyltransferase inhibitor Kohl,N.E.;S.D.Mosser;S.J.Desolms;E.A.Giuliani;D.L.Pompliano;S.L.Graham;R.L.Smith;E.M.Scolnick;A.Oliff;j.B.Gibbs
  15. Science v.260 Benzodiazepine peptidomimetics: potent inhibitors of Ras farnesylation in animal cells James,G.L.;J.L.Goldstein;M.S.Brown;T.E.Rawson;T.C.Sommers;R.S.McDowell;C.W.Crowley;B.K.Lukas;A.D.Levinson;J.C.Marsters