Suppression of DNA Synthesis in Hepatoma Cells Exposed to Glucocorticoid Hormone in Vitro

Glucocorticoid hormone is shown to markedly suppress DNA synthesis in a line of rat hepatoma cells in vitro. In the presence of 300 nM hydrocortisone or 30 nM dexamethasone the incorporation of radioactive thymidine falls to 50% of control levels by 36 hr, and at higher concentrations of hormone inh...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1973-12, Vol.70 (12), p.3852-3856
Hauptverfasser: Loeb, John N., Borek, Carmia, Yeung, Lucy L.
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Borek, Carmia
Yeung, Lucy L.
description Glucocorticoid hormone is shown to markedly suppress DNA synthesis in a line of rat hepatoma cells in vitro. In the presence of 300 nM hydrocortisone or 30 nM dexamethasone the incorporation of radioactive thymidine falls to 50% of control levels by 36 hr, and at higher concentrations of hormone inhibition can be noted as early as 12 hr and is nearly complete by 24 hr. This inhibition of radioactive thymidine incorporation reflects a true suppression of DNA synthesis, is accompanied by a corresponding inhibition of cell proliferation, and is readily reversible upon subsequent removal of hormone. In contrast to previously described effects of the glucocorticoid hormones on various cells of lymphoid origin, the inhibition of DNA synthesis in these hepatoma cells is not accompanied by appreciable cell lysis or by degradation of preformed DNA, and even when [3H]thymidine incorporation into DNA is inhibited by 90% or more, incorporation of [14C]uridine into RNA proceeds with little change. These findings all parallel previous observations on the effects of glucocorticoid hormone on the livers of intact animals and suggest that studies on the mechanism of the inhibition of DNA synthesis in the present more isolated system may lead to a better understanding of the means by which these compounds inhibit liver growth in vivo. Despite the ready suppressibility of DNA synthesis in these hepatoma cells and in two other cell lines of liver origin, none of these cell lines was found to be inducible for tyrosine aminotransferase. The apparent dissociation between two ``steroid-sensitive'' phenomena is of interest and warrants further investigation.
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In the presence of 300 nM hydrocortisone or 30 nM dexamethasone the incorporation of radioactive thymidine falls to 50% of control levels by 36 hr, and at higher concentrations of hormone inhibition can be noted as early as 12 hr and is nearly complete by 24 hr. This inhibition of radioactive thymidine incorporation reflects a true suppression of DNA synthesis, is accompanied by a corresponding inhibition of cell proliferation, and is readily reversible upon subsequent removal of hormone. In contrast to previously described effects of the glucocorticoid hormones on various cells of lymphoid origin, the inhibition of DNA synthesis in these hepatoma cells is not accompanied by appreciable cell lysis or by degradation of preformed DNA, and even when [3H]thymidine incorporation into DNA is inhibited by 90% or more, incorporation of [14C]uridine into RNA proceeds with little change. These findings all parallel previous observations on the effects of glucocorticoid hormone on the livers of intact animals and suggest that studies on the mechanism of the inhibition of DNA synthesis in the present more isolated system may lead to a better understanding of the means by which these compounds inhibit liver growth in vivo. Despite the ready suppressibility of DNA synthesis in these hepatoma cells and in two other cell lines of liver origin, none of these cell lines was found to be inducible for tyrosine aminotransferase. 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In the presence of 300 nM hydrocortisone or 30 nM dexamethasone the incorporation of radioactive thymidine falls to 50% of control levels by 36 hr, and at higher concentrations of hormone inhibition can be noted as early as 12 hr and is nearly complete by 24 hr. This inhibition of radioactive thymidine incorporation reflects a true suppression of DNA synthesis, is accompanied by a corresponding inhibition of cell proliferation, and is readily reversible upon subsequent removal of hormone. In contrast to previously described effects of the glucocorticoid hormones on various cells of lymphoid origin, the inhibition of DNA synthesis in these hepatoma cells is not accompanied by appreciable cell lysis or by degradation of preformed DNA, and even when [3H]thymidine incorporation into DNA is inhibited by 90% or more, incorporation of [14C]uridine into RNA proceeds with little change. These findings all parallel previous observations on the effects of glucocorticoid hormone on the livers of intact animals and suggest that studies on the mechanism of the inhibition of DNA synthesis in the present more isolated system may lead to a better understanding of the means by which these compounds inhibit liver growth in vivo. Despite the ready suppressibility of DNA synthesis in these hepatoma cells and in two other cell lines of liver origin, none of these cell lines was found to be inducible for tyrosine aminotransferase. The apparent dissociation between two ``steroid-sensitive'' phenomena is of interest and warrants further investigation.</description><subject>Animals</subject><subject>Biological Sciences: Cell Biology</subject><subject>Carbon Radioisotopes</subject><subject>Carcinoma, Hepatocellular - enzymology</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Cell Line</subject><subject>Cell lines</subject><subject>Depression, Chemical</subject><subject>Dexamethasone - pharmacology</subject><subject>DNA</subject><subject>DNA, Neoplasm - biosynthesis</subject><subject>Ethanol</subject><subject>Glucocorticoids</subject><subject>Hepatocellular carcinoma</subject><subject>Hepatocytes</subject><subject>Hormones</subject><subject>Hydrocortisone - pharmacology</subject><subject>Kinetics</subject><subject>Liver</subject><subject>Liver cells</subject><subject>Liver Neoplasms - enzymology</subject><subject>Liver Neoplasms - metabolism</subject><subject>Neoplasms, Experimental - metabolism</subject><subject>Rats</subject><subject>RNA</subject><subject>RNA, Neoplasm - biosynthesis</subject><subject>Thymidine - metabolism</subject><subject>Tritium</subject><subject>Tyrosine Transaminase - metabolism</subject><subject>Uridine - metabolism</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1v1DAQxS0EKsvCGQkJ5BM9ZevPJD5wqJbSRargUEDiZDnOhLpK4mA7qP3vcbTbBS6c7NH7vZmxH0IvKdlQUvGzaTRxU-WCbXgt2SO0okTRohSKPEYrQlhV1IKJp-hZjLeEECVrcoJOBBVKcLlC36_naQoQo_Mj9h1-_-kcX9-P6Qaii9iNeAeTSX4weAt9H_HF3eQjtDh5fNnP1lsfkrPetXjnw-BHWDzfXAr-OXrSmT7Ci8O5Rl8_XHzZ7oqrz5cft-dXhRUlTUUtVdtYpqQQpqXSUAAFgnOppLKybKBTSrC2Yw1I0nS27iS0os7XVlWlEXyN3u37TnMzQGthTMH0egpuMOFee-P0v8robvQP_0sLVvE8aI3eHvzB_5whJj24aPNjzQh-jrpmVNY1lxk824M2-BgDdMcZlOglDL2EoatcML2EkR2v_17tyB9-P-unB30xPqh_Guhu7vsEdymTb_5LZuDVHriNyYcjUbKyFPw3jQSo1g</recordid><startdate>19731201</startdate><enddate>19731201</enddate><creator>Loeb, John N.</creator><creator>Borek, Carmia</creator><creator>Yeung, Lucy L.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><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><scope>5PM</scope></search><sort><creationdate>19731201</creationdate><title>Suppression of DNA Synthesis in Hepatoma Cells Exposed to Glucocorticoid Hormone in Vitro</title><author>Loeb, John N. ; Borek, Carmia ; Yeung, Lucy L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-859dbc29544ad15a1ee9e4335959c56bef9942df2be50bfc8f5ed480bfd976a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><topic>Animals</topic><topic>Biological Sciences: Cell Biology</topic><topic>Carbon Radioisotopes</topic><topic>Carcinoma, Hepatocellular - enzymology</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Cell Line</topic><topic>Cell lines</topic><topic>Depression, Chemical</topic><topic>Dexamethasone - pharmacology</topic><topic>DNA</topic><topic>DNA, Neoplasm - biosynthesis</topic><topic>Ethanol</topic><topic>Glucocorticoids</topic><topic>Hepatocellular carcinoma</topic><topic>Hepatocytes</topic><topic>Hormones</topic><topic>Hydrocortisone - pharmacology</topic><topic>Kinetics</topic><topic>Liver</topic><topic>Liver cells</topic><topic>Liver Neoplasms - enzymology</topic><topic>Liver Neoplasms - metabolism</topic><topic>Neoplasms, Experimental - metabolism</topic><topic>Rats</topic><topic>RNA</topic><topic>RNA, Neoplasm - biosynthesis</topic><topic>Thymidine - metabolism</topic><topic>Tritium</topic><topic>Tyrosine Transaminase - metabolism</topic><topic>Uridine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Loeb, John N.</creatorcontrib><creatorcontrib>Borek, Carmia</creatorcontrib><creatorcontrib>Yeung, Lucy L.</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Loeb, John N.</au><au>Borek, Carmia</au><au>Yeung, Lucy L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppression of DNA Synthesis in Hepatoma Cells Exposed to Glucocorticoid Hormone in Vitro</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1973-12-01</date><risdate>1973</risdate><volume>70</volume><issue>12</issue><spage>3852</spage><epage>3856</epage><pages>3852-3856</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Glucocorticoid hormone is shown to markedly suppress DNA synthesis in a line of rat hepatoma cells in vitro. In the presence of 300 nM hydrocortisone or 30 nM dexamethasone the incorporation of radioactive thymidine falls to 50% of control levels by 36 hr, and at higher concentrations of hormone inhibition can be noted as early as 12 hr and is nearly complete by 24 hr. This inhibition of radioactive thymidine incorporation reflects a true suppression of DNA synthesis, is accompanied by a corresponding inhibition of cell proliferation, and is readily reversible upon subsequent removal of hormone. In contrast to previously described effects of the glucocorticoid hormones on various cells of lymphoid origin, the inhibition of DNA synthesis in these hepatoma cells is not accompanied by appreciable cell lysis or by degradation of preformed DNA, and even when [3H]thymidine incorporation into DNA is inhibited by 90% or more, incorporation of [14C]uridine into RNA proceeds with little change. These findings all parallel previous observations on the effects of glucocorticoid hormone on the livers of intact animals and suggest that studies on the mechanism of the inhibition of DNA synthesis in the present more isolated system may lead to a better understanding of the means by which these compounds inhibit liver growth in vivo. Despite the ready suppressibility of DNA synthesis in these hepatoma cells and in two other cell lines of liver origin, none of these cell lines was found to be inducible for tyrosine aminotransferase. The apparent dissociation between two ``steroid-sensitive'' phenomena is of interest and warrants further investigation.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>4149435</pmid><doi>10.1073/pnas.70.12.3852</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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source Jstor Complete Legacy; MEDLINE; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Animals
Biological Sciences: Cell Biology
Carbon Radioisotopes
Carcinoma, Hepatocellular - enzymology
Carcinoma, Hepatocellular - metabolism
Cell Line
Cell lines
Depression, Chemical
Dexamethasone - pharmacology
DNA
DNA, Neoplasm - biosynthesis
Ethanol
Glucocorticoids
Hepatocellular carcinoma
Hepatocytes
Hormones
Hydrocortisone - pharmacology
Kinetics
Liver
Liver cells
Liver Neoplasms - enzymology
Liver Neoplasms - metabolism
Neoplasms, Experimental - metabolism
Rats
RNA
RNA, Neoplasm - biosynthesis
Thymidine - metabolism
Tritium
Tyrosine Transaminase - metabolism
Uridine - metabolism
title Suppression of DNA Synthesis in Hepatoma Cells Exposed to Glucocorticoid Hormone in Vitro
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