alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines
In order to assess the tolerance of the target enzyme spermine synthase for alpha-substituents on the aminopropyl moiety of the substrate spermidine, 1-methylspermidine (MeSpd, 2) was synthesized. It was determined that MeSpd is a poor substrate for spermine synthase and is not a substrate for sperm...
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Veröffentlicht in: | Journal of medicinal chemistry 1992-02, Vol.35 (4), p.724-734 |
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description | In order to assess the tolerance of the target enzyme spermine synthase for alpha-substituents on the aminopropyl moiety of the substrate spermidine, 1-methylspermidine (MeSpd, 2) was synthesized. It was determined that MeSpd is a poor substrate for spermine synthase and is not a substrate for spermidine N1-acetyltransferase, suggesting that alpha-methylated polyamines might be metabolically stable and therefore useful tools for studying polyamine effects in intact cells. On the basis of initial cellular results with 2, 1-methylspermine (MeSpm, 3) and 1,12-dimethylspermine (Me2Spm, 4) were also synthesized. When added to cells (L1210, SV-3T3, or HT29) depleted of both putrescine and spermidine by prior treatment with alpha-(difluoromethyl)ornithine (DFMO), these alpha-methylated polyamines were able to restore cell growth to that observed in the absence of DFMO. In accord with the enzyme data noted above, metabolic studies indicated a slow conversion of 2 to 3, but no metabolism of 4 in these cells. It was concluded from these results that the alpha-methylated polyamines are able to substitute for the natural polyamines spermidine and spermine in critical biochemical processes which involve polyamines for continued cell growth. In accord with the hypothesis, preliminary data indicate that MeSpd and Me2Spm are as effective as spermidine and spermine, respectively, in promoting the conversion of B-DNA to Z-DNA. |
doi_str_mv | 10.1021/jm00082a013 |
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It was determined that MeSpd is a poor substrate for spermine synthase and is not a substrate for spermidine N1-acetyltransferase, suggesting that alpha-methylated polyamines might be metabolically stable and therefore useful tools for studying polyamine effects in intact cells. On the basis of initial cellular results with 2, 1-methylspermine (MeSpm, 3) and 1,12-dimethylspermine (Me2Spm, 4) were also synthesized. When added to cells (L1210, SV-3T3, or HT29) depleted of both putrescine and spermidine by prior treatment with alpha-(difluoromethyl)ornithine (DFMO), these alpha-methylated polyamines were able to restore cell growth to that observed in the absence of DFMO. In accord with the enzyme data noted above, metabolic studies indicated a slow conversion of 2 to 3, but no metabolism of 4 in these cells. It was concluded from these results that the alpha-methylated polyamines are able to substitute for the natural polyamines spermidine and spermine in critical biochemical processes which involve polyamines for continued cell growth. In accord with the hypothesis, preliminary data indicate that MeSpd and Me2Spm are as effective as spermidine and spermine, respectively, in promoting the conversion of B-DNA to Z-DNA.</description><identifier>ISSN: 0022-2623</identifier><identifier>EISSN: 1520-4804</identifier><identifier>DOI: 10.1021/jm00082a013</identifier><identifier>PMID: 1542099</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Cell Division - drug effects ; Cell Line, Transformed ; Colonic Neoplasms - pathology ; Eflornithine - pharmacology ; Humans ; Leukemia L1210 - metabolism ; Leukemia L1210 - pathology ; Methylation ; Mice ; Putrescine - metabolism ; Spermidine - analogs & derivatives ; Spermidine - chemical synthesis ; Spermidine - metabolism ; Spermidine - pharmacology ; Spermine - analogs & derivatives ; Spermine - chemical synthesis ; Spermine - metabolism ; Spermine - pharmacology ; Spermine Synthase - metabolism ; Substrate Specificity ; Tumor Cells, Cultured</subject><ispartof>Journal of medicinal chemistry, 1992-02, Vol.35 (4), p.724-734</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a354t-ab7d0d70b4177638121e6be104699fa4a0fc21864f037eaa787de2920e2717c63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jm00082a013$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jm00082a013$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1542099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lakanen, John R</creatorcontrib><creatorcontrib>Coward, James K</creatorcontrib><creatorcontrib>Pegg, Anthony E</creatorcontrib><title>alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines</title><title>Journal of medicinal chemistry</title><addtitle>J. Med. Chem</addtitle><description>In order to assess the tolerance of the target enzyme spermine synthase for alpha-substituents on the aminopropyl moiety of the substrate spermidine, 1-methylspermidine (MeSpd, 2) was synthesized. It was determined that MeSpd is a poor substrate for spermine synthase and is not a substrate for spermidine N1-acetyltransferase, suggesting that alpha-methylated polyamines might be metabolically stable and therefore useful tools for studying polyamine effects in intact cells. On the basis of initial cellular results with 2, 1-methylspermine (MeSpm, 3) and 1,12-dimethylspermine (Me2Spm, 4) were also synthesized. When added to cells (L1210, SV-3T3, or HT29) depleted of both putrescine and spermidine by prior treatment with alpha-(difluoromethyl)ornithine (DFMO), these alpha-methylated polyamines were able to restore cell growth to that observed in the absence of DFMO. In accord with the enzyme data noted above, metabolic studies indicated a slow conversion of 2 to 3, but no metabolism of 4 in these cells. It was concluded from these results that the alpha-methylated polyamines are able to substitute for the natural polyamines spermidine and spermine in critical biochemical processes which involve polyamines for continued cell growth. In accord with the hypothesis, preliminary data indicate that MeSpd and Me2Spm are as effective as spermidine and spermine, respectively, in promoting the conversion of B-DNA to Z-DNA.</description><subject>Animals</subject><subject>Cell Division - drug effects</subject><subject>Cell Line, Transformed</subject><subject>Colonic Neoplasms - pathology</subject><subject>Eflornithine - pharmacology</subject><subject>Humans</subject><subject>Leukemia L1210 - metabolism</subject><subject>Leukemia L1210 - pathology</subject><subject>Methylation</subject><subject>Mice</subject><subject>Putrescine - metabolism</subject><subject>Spermidine - analogs & derivatives</subject><subject>Spermidine - chemical synthesis</subject><subject>Spermidine - metabolism</subject><subject>Spermidine - pharmacology</subject><subject>Spermine - analogs & derivatives</subject><subject>Spermine - chemical synthesis</subject><subject>Spermine - metabolism</subject><subject>Spermine - pharmacology</subject><subject>Spermine Synthase - metabolism</subject><subject>Substrate Specificity</subject><subject>Tumor Cells, Cultured</subject><issn>0022-2623</issn><issn>1520-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E1v1DAQBmALgcpSOHFG8gkOKMVfiRNuVfmsigBRztYkmXS92LGxE8H-BX41WbKiHDhZr-bRjPUS8pizM84Ef7HzjLFaAOPyDtnwUrBC1UzdJRvGhChEJeR98iDn3cIkF_KEnPBSCdY0G_ILXNzCWfEBp-3e0RjcHrwdMb-kHidog7MdOLeneQkOaY6YvO0XQWHsj3EJ3nrbZdpB_MPCQPMcY0iTHW_oTQo_pi21I-3QuUx7jA4n7A_s9uJDcm8Al_HR8T0lX9-8vr54V1x9fPv-4vyqAFmqqYBW96zXrFVc60rWXHCsWuRMVU0zgAI2dILXlRqY1Aiga92jaARDobnuKnlKnq57YwrfZ8yT8TYfPgYjhjkbLWrFS3mAz1fYpZBzwsHEZD2kveHMHJo3_zS_6CfHtXPrsb-1a9XLvFjnNk_48-8Y0jdTaalLc_3pi-GyvOTq86V5tfhnq4cum12Y07iU8t_LvwGmApvI</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>Lakanen, John R</creator><creator>Coward, James K</creator><creator>Pegg, Anthony E</creator><general>American Chemical Society</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>19920201</creationdate><title>alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines</title><author>Lakanen, John R ; Coward, James K ; Pegg, Anthony E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a354t-ab7d0d70b4177638121e6be104699fa4a0fc21864f037eaa787de2920e2717c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Cell Division - drug effects</topic><topic>Cell Line, Transformed</topic><topic>Colonic Neoplasms - pathology</topic><topic>Eflornithine - pharmacology</topic><topic>Humans</topic><topic>Leukemia L1210 - metabolism</topic><topic>Leukemia L1210 - pathology</topic><topic>Methylation</topic><topic>Mice</topic><topic>Putrescine - metabolism</topic><topic>Spermidine - analogs & derivatives</topic><topic>Spermidine - chemical synthesis</topic><topic>Spermidine - metabolism</topic><topic>Spermidine - pharmacology</topic><topic>Spermine - analogs & derivatives</topic><topic>Spermine - chemical synthesis</topic><topic>Spermine - metabolism</topic><topic>Spermine - pharmacology</topic><topic>Spermine Synthase - metabolism</topic><topic>Substrate Specificity</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lakanen, John R</creatorcontrib><creatorcontrib>Coward, James K</creatorcontrib><creatorcontrib>Pegg, Anthony E</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lakanen, John R</au><au>Coward, James K</au><au>Pegg, Anthony E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. Med. Chem</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>35</volume><issue>4</issue><spage>724</spage><epage>734</epage><pages>724-734</pages><issn>0022-2623</issn><eissn>1520-4804</eissn><abstract>In order to assess the tolerance of the target enzyme spermine synthase for alpha-substituents on the aminopropyl moiety of the substrate spermidine, 1-methylspermidine (MeSpd, 2) was synthesized. It was determined that MeSpd is a poor substrate for spermine synthase and is not a substrate for spermidine N1-acetyltransferase, suggesting that alpha-methylated polyamines might be metabolically stable and therefore useful tools for studying polyamine effects in intact cells. On the basis of initial cellular results with 2, 1-methylspermine (MeSpm, 3) and 1,12-dimethylspermine (Me2Spm, 4) were also synthesized. When added to cells (L1210, SV-3T3, or HT29) depleted of both putrescine and spermidine by prior treatment with alpha-(difluoromethyl)ornithine (DFMO), these alpha-methylated polyamines were able to restore cell growth to that observed in the absence of DFMO. In accord with the enzyme data noted above, metabolic studies indicated a slow conversion of 2 to 3, but no metabolism of 4 in these cells. It was concluded from these results that the alpha-methylated polyamines are able to substitute for the natural polyamines spermidine and spermine in critical biochemical processes which involve polyamines for continued cell growth. In accord with the hypothesis, preliminary data indicate that MeSpd and Me2Spm are as effective as spermidine and spermine, respectively, in promoting the conversion of B-DNA to Z-DNA.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>1542099</pmid><doi>10.1021/jm00082a013</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Cell Division - drug effects Cell Line, Transformed Colonic Neoplasms - pathology Eflornithine - pharmacology Humans Leukemia L1210 - metabolism Leukemia L1210 - pathology Methylation Mice Putrescine - metabolism Spermidine - analogs & derivatives Spermidine - chemical synthesis Spermidine - metabolism Spermidine - pharmacology Spermine - analogs & derivatives Spermine - chemical synthesis Spermine - metabolism Spermine - pharmacology Spermine Synthase - metabolism Substrate Specificity Tumor Cells, Cultured |
title | alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines |
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