Loading…

Anticancer and Some Biological Activities of Thiazinotrienomycin B

As a primary screening system for new anticancer antibiotics, we have been using several cancer cell lines of human origins and selecting microbial products that are growth-inhibitory in vitro to certain cell lines, rather than to all the cell lines, to avoid compounds of nonspecific toxicity. Thiaz...

Full description

Saved in:
Bibliographic Details
Published in:Journal of antibiotics 2000/03/25, Vol.53(3), pp.306-308
Main Authors: HOSOKAWA, NOBUO, IINUMA, HIRONOBU, TAKEUCHI, TOMIO, SATO, SHIGEO, YAMORI, TAKAO, TSUCHIYA, KAYOKO S., HORI, MAKOTO
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c667t-f12a96dc97b452f5b19a032d6036bcd067bc3e1c6c7129297ee870d17f9bad013
cites
container_end_page 308
container_issue 3
container_start_page 306
container_title Journal of antibiotics
container_volume 53
creator HOSOKAWA, NOBUO
IINUMA, HIRONOBU
TAKEUCHI, TOMIO
SATO, SHIGEO
YAMORI, TAKAO
TSUCHIYA, KAYOKO S.
HORI, MAKOTO
description As a primary screening system for new anticancer antibiotics, we have been using several cancer cell lines of human origins and selecting microbial products that are growth-inhibitory in vitro to certain cell lines, rather than to all the cell lines, to avoid compounds of nonspecific toxicity. Thiazinotrienomycins were isolated for their activities somewhat specific to HeLa than to other cell lines which were available to us at the time of our investigation. Thiazinotrienomycin B (referred to as TT-B), a minor member in quantity, turned out to be the strongest in inhibiting growth in vitro of HeLa cells. In the present paper, we report the pattern of differential growth inhibition in vitro by TT-B of a disease-oriented panel of human tumor cell lines and the inhibition by TT-B of xenograft of BSY-1 (breast) in nude mice.
doi_str_mv 10.7164/antibiotics.53.306
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71122548</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71122548</sourcerecordid><originalsourceid>FETCH-LOGICAL-c667t-f12a96dc97b452f5b19a032d6036bcd067bc3e1c6c7129297ee870d17f9bad013</originalsourceid><addsrcrecordid>eNqFkE1PxCAURYnR6Dj6B1yYLoy7jjxo-VjOTPyKJi7UNaGUKqYtCh0T_fWinejs3EAC5937chA6AjzjwIoz3Q-ucn5wJs5KOqOYbaEJCAE5FExuownGBHIhCN5D-zG-YEw55WIX7QEWICkuJmgxTyFG98aGTPd1du87my2cb_1Tem6zuRncuxucjZlvsodnpz9d74fgbO-7D-P6bHGAdhrdRnu4vqfo8eL8YXmV395dXi_nt7lhjA95A0RLVhvJq6IkTVmB1JiSmmHKKlNjxitDLRhmOBBJJLdWcFwDb2Slawx0ik7H3Nfg31Y2Dqpz0di21b31q6g4ACFlIf4FgZdlSVPvFJERNMHHGGyjXoPrdPhQgNW3YrWhWJVUJcVp6Hidvqo6W2-MjE4TcLIGdEwKm5DsuvjHUcY5_8ZuRuwlDvrJ_v7rkNpau1kNkomf-vFIW_xS5lkHZXv6Bf2bohI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17555360</pqid></control><display><type>article</type><title>Anticancer and Some Biological Activities of Thiazinotrienomycin B</title><source>J-STAGE Freely Available Titles - English</source><creator>HOSOKAWA, NOBUO ; IINUMA, HIRONOBU ; TAKEUCHI, TOMIO ; SATO, SHIGEO ; YAMORI, TAKAO ; TSUCHIYA, KAYOKO S. ; HORI, MAKOTO</creator><creatorcontrib>HOSOKAWA, NOBUO ; IINUMA, HIRONOBU ; TAKEUCHI, TOMIO ; SATO, SHIGEO ; YAMORI, TAKAO ; TSUCHIYA, KAYOKO S. ; HORI, MAKOTO</creatorcontrib><description>As a primary screening system for new anticancer antibiotics, we have been using several cancer cell lines of human origins and selecting microbial products that are growth-inhibitory in vitro to certain cell lines, rather than to all the cell lines, to avoid compounds of nonspecific toxicity. Thiazinotrienomycins were isolated for their activities somewhat specific to HeLa than to other cell lines which were available to us at the time of our investigation. Thiazinotrienomycin B (referred to as TT-B), a minor member in quantity, turned out to be the strongest in inhibiting growth in vitro of HeLa cells. In the present paper, we report the pattern of differential growth inhibition in vitro by TT-B of a disease-oriented panel of human tumor cell lines and the inhibition by TT-B of xenograft of BSY-1 (breast) in nude mice.</description><identifier>ISSN: 0021-8820</identifier><identifier>EISSN: 1881-1469</identifier><identifier>DOI: 10.7164/antibiotics.53.306</identifier><identifier>PMID: 10819304</identifier><identifier>CODEN: JANTAJ</identifier><language>eng</language><publisher>Tokyo: JAPAN ANTIBIOTICS RESEARCH ASSOCIATION</publisher><subject>Animals ; Antibiotics, Antineoplastic - pharmacology ; Antineoplastic agents ; Biological and medical sciences ; Cell Division - drug effects ; General aspects ; Graft Survival - drug effects ; Humans ; Medical sciences ; Mice ; Mice, Nude ; Neoplasm Transplantation ; Neoplasms, Experimental - drug therapy ; Neoplasms, Experimental - pathology ; Pharmacology. Drug treatments ; Random Allocation ; Thiazines - pharmacology ; thiazinotrienomycin B ; Transplantation, Heterologous ; Tumor Cells, Cultured - drug effects</subject><ispartof>The Journal of Antibiotics, 2000/03/25, Vol.53(3), pp.306-308</ispartof><rights>Japan Antibiotics Research Association</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c667t-f12a96dc97b452f5b19a032d6036bcd067bc3e1c6c7129297ee870d17f9bad013</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1882,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1367774$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10819304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HOSOKAWA, NOBUO</creatorcontrib><creatorcontrib>IINUMA, HIRONOBU</creatorcontrib><creatorcontrib>TAKEUCHI, TOMIO</creatorcontrib><creatorcontrib>SATO, SHIGEO</creatorcontrib><creatorcontrib>YAMORI, TAKAO</creatorcontrib><creatorcontrib>TSUCHIYA, KAYOKO S.</creatorcontrib><creatorcontrib>HORI, MAKOTO</creatorcontrib><title>Anticancer and Some Biological Activities of Thiazinotrienomycin B</title><title>Journal of antibiotics</title><addtitle>J. Antibiot.</addtitle><description>As a primary screening system for new anticancer antibiotics, we have been using several cancer cell lines of human origins and selecting microbial products that are growth-inhibitory in vitro to certain cell lines, rather than to all the cell lines, to avoid compounds of nonspecific toxicity. Thiazinotrienomycins were isolated for their activities somewhat specific to HeLa than to other cell lines which were available to us at the time of our investigation. Thiazinotrienomycin B (referred to as TT-B), a minor member in quantity, turned out to be the strongest in inhibiting growth in vitro of HeLa cells. In the present paper, we report the pattern of differential growth inhibition in vitro by TT-B of a disease-oriented panel of human tumor cell lines and the inhibition by TT-B of xenograft of BSY-1 (breast) in nude mice.</description><subject>Animals</subject><subject>Antibiotics, Antineoplastic - pharmacology</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Cell Division - drug effects</subject><subject>General aspects</subject><subject>Graft Survival - drug effects</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Neoplasm Transplantation</subject><subject>Neoplasms, Experimental - drug therapy</subject><subject>Neoplasms, Experimental - pathology</subject><subject>Pharmacology. Drug treatments</subject><subject>Random Allocation</subject><subject>Thiazines - pharmacology</subject><subject>thiazinotrienomycin B</subject><subject>Transplantation, Heterologous</subject><subject>Tumor Cells, Cultured - drug effects</subject><issn>0021-8820</issn><issn>1881-1469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PxCAURYnR6Dj6B1yYLoy7jjxo-VjOTPyKJi7UNaGUKqYtCh0T_fWinejs3EAC5937chA6AjzjwIoz3Q-ucn5wJs5KOqOYbaEJCAE5FExuownGBHIhCN5D-zG-YEw55WIX7QEWICkuJmgxTyFG98aGTPd1du87my2cb_1Tem6zuRncuxucjZlvsodnpz9d74fgbO-7D-P6bHGAdhrdRnu4vqfo8eL8YXmV395dXi_nt7lhjA95A0RLVhvJq6IkTVmB1JiSmmHKKlNjxitDLRhmOBBJJLdWcFwDb2Slawx0ik7H3Nfg31Y2Dqpz0di21b31q6g4ACFlIf4FgZdlSVPvFJERNMHHGGyjXoPrdPhQgNW3YrWhWJVUJcVp6Hidvqo6W2-MjE4TcLIGdEwKm5DsuvjHUcY5_8ZuRuwlDvrJ_v7rkNpau1kNkomf-vFIW_xS5lkHZXv6Bf2bohI</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>HOSOKAWA, NOBUO</creator><creator>IINUMA, HIRONOBU</creator><creator>TAKEUCHI, TOMIO</creator><creator>SATO, SHIGEO</creator><creator>YAMORI, TAKAO</creator><creator>TSUCHIYA, KAYOKO S.</creator><creator>HORI, MAKOTO</creator><general>JAPAN ANTIBIOTICS RESEARCH ASSOCIATION</general><general>Japan Antibiotics Research Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2000</creationdate><title>Anticancer and Some Biological Activities of Thiazinotrienomycin B</title><author>HOSOKAWA, NOBUO ; IINUMA, HIRONOBU ; TAKEUCHI, TOMIO ; SATO, SHIGEO ; YAMORI, TAKAO ; TSUCHIYA, KAYOKO S. ; HORI, MAKOTO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c667t-f12a96dc97b452f5b19a032d6036bcd067bc3e1c6c7129297ee870d17f9bad013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Antibiotics, Antineoplastic - pharmacology</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Cell Division - drug effects</topic><topic>General aspects</topic><topic>Graft Survival - drug effects</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Neoplasm Transplantation</topic><topic>Neoplasms, Experimental - drug therapy</topic><topic>Neoplasms, Experimental - pathology</topic><topic>Pharmacology. Drug treatments</topic><topic>Random Allocation</topic><topic>Thiazines - pharmacology</topic><topic>thiazinotrienomycin B</topic><topic>Transplantation, Heterologous</topic><topic>Tumor Cells, Cultured - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HOSOKAWA, NOBUO</creatorcontrib><creatorcontrib>IINUMA, HIRONOBU</creatorcontrib><creatorcontrib>TAKEUCHI, TOMIO</creatorcontrib><creatorcontrib>SATO, SHIGEO</creatorcontrib><creatorcontrib>YAMORI, TAKAO</creatorcontrib><creatorcontrib>TSUCHIYA, KAYOKO S.</creatorcontrib><creatorcontrib>HORI, MAKOTO</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HOSOKAWA, NOBUO</au><au>IINUMA, HIRONOBU</au><au>TAKEUCHI, TOMIO</au><au>SATO, SHIGEO</au><au>YAMORI, TAKAO</au><au>TSUCHIYA, KAYOKO S.</au><au>HORI, MAKOTO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anticancer and Some Biological Activities of Thiazinotrienomycin B</atitle><jtitle>Journal of antibiotics</jtitle><addtitle>J. Antibiot.</addtitle><date>2000</date><risdate>2000</risdate><volume>53</volume><issue>3</issue><spage>306</spage><epage>308</epage><pages>306-308</pages><issn>0021-8820</issn><eissn>1881-1469</eissn><coden>JANTAJ</coden><abstract>As a primary screening system for new anticancer antibiotics, we have been using several cancer cell lines of human origins and selecting microbial products that are growth-inhibitory in vitro to certain cell lines, rather than to all the cell lines, to avoid compounds of nonspecific toxicity. Thiazinotrienomycins were isolated for their activities somewhat specific to HeLa than to other cell lines which were available to us at the time of our investigation. Thiazinotrienomycin B (referred to as TT-B), a minor member in quantity, turned out to be the strongest in inhibiting growth in vitro of HeLa cells. In the present paper, we report the pattern of differential growth inhibition in vitro by TT-B of a disease-oriented panel of human tumor cell lines and the inhibition by TT-B of xenograft of BSY-1 (breast) in nude mice.</abstract><cop>Tokyo</cop><pub>JAPAN ANTIBIOTICS RESEARCH ASSOCIATION</pub><pmid>10819304</pmid><doi>10.7164/antibiotics.53.306</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-8820
ispartof The Journal of Antibiotics, 2000/03/25, Vol.53(3), pp.306-308
issn 0021-8820
1881-1469
language eng
recordid cdi_proquest_miscellaneous_71122548
source J-STAGE Freely Available Titles - English
subjects Animals
Antibiotics, Antineoplastic - pharmacology
Antineoplastic agents
Biological and medical sciences
Cell Division - drug effects
General aspects
Graft Survival - drug effects
Humans
Medical sciences
Mice
Mice, Nude
Neoplasm Transplantation
Neoplasms, Experimental - drug therapy
Neoplasms, Experimental - pathology
Pharmacology. Drug treatments
Random Allocation
Thiazines - pharmacology
thiazinotrienomycin B
Transplantation, Heterologous
Tumor Cells, Cultured - drug effects
title Anticancer and Some Biological Activities of Thiazinotrienomycin B
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T06%3A31%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Anticancer%20and%20Some%20Biological%20Activities%20of%20Thiazinotrienomycin%20B&rft.jtitle=Journal%20of%20antibiotics&rft.au=HOSOKAWA,%20NOBUO&rft.date=2000&rft.volume=53&rft.issue=3&rft.spage=306&rft.epage=308&rft.pages=306-308&rft.issn=0021-8820&rft.eissn=1881-1469&rft.coden=JANTAJ&rft_id=info:doi/10.7164/antibiotics.53.306&rft_dat=%3Cproquest_cross%3E71122548%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c667t-f12a96dc97b452f5b19a032d6036bcd067bc3e1c6c7129297ee870d17f9bad013%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=17555360&rft_id=info:pmid/10819304&rfr_iscdi=true