<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Q</submitter><funding>NCI NIH HHS</funding><pagination>1066-71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6007862</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(6)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To compare the chemopreventive efficacy of Polyphenon E (Poly E), (-)-epigallocatechin-3-gallate (EGCG) and Polyphenon E without EGCG (Poly E-EGCG) on the development of benzo(a)pyrene (B(a)P)-induced lung tumors in A/J mice.&lt;h4>Methods&lt;/h4>Female A/J mice were given a single intraperitoneal injection of B(a)P (100 mg/kg body weight). One week after B(a)P injection, animals received AIN-76A purified powder diet containing 0.975% (wt/wt) EGCG, 0.525% (wt/wt) Poly E-EGCG or 1.5% (wt/wt) Poly E for 24 weeks or control diet with no additives.&lt;h4>Results&lt;/h4>Poly E treatment significantly decreased tumor multiplicity by 52% and tumor load by 64%, while EGCG and Poly E-EGCG did not significantly inhibit lung tumor multiplicity. EGCG was more stable in a complex mixture (Poly E) t</pubmed_abstract><journal>Pharmaceutical research</journal><pubmed_title>Effect of dietary Polyphenon E and EGCG on lung tumorigenesis in A/J Mice.</pubmed_title><pmcid>PMC6007862</pmcid><funding_grant_id>R01CA139959</funding_grant_id><funding_grant_id>R01 CA139959</funding_grant_id><pubmed_authors>Pan J</pubmed_authors><pubmed_authors>Ryota S</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Fu H</pubmed_authors><pubmed_authors>Lubet RA</pubmed_authors><pubmed_authors>You M</pubmed_authors><pubmed_authors>Hara Y</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of dietary Polyphenon E and EGCG on lung tumorigenesis in A/J Mice.</name><description>&lt;h4>Purpose&lt;/h4>To compare the chemopreventive efficacy of Polyphenon E (Poly E), (-)-epigallocatechin-3-gallate (EGCG) and Polyphenon E without EGCG (Poly E-EGCG) on the development of benzo(a)pyrene (B(a)P)-induced lung tumors in A/J mice.&lt;h4>Methods&lt;/h4>Female A/J mice were given a single intraperitoneal injection of B(a)P (100 mg/kg body weight). One week after B(a)P injection, animals received AIN-76A purified powder diet containing 0.975% (wt/wt) EGCG, 0.525% (wt/wt) Poly E-EGCG or 1.5% (wt/wt) Poly E for 24 weeks or control diet with no additives.&lt;h4>Results&lt;/h4>Poly E treatment significantly decreased tumor multiplicity by 52% and tumor load by 64%, while EGCG and Poly E-EGCG did not significantly inhibit lung tumor multiplicity. EGCG was more stable in a complex mixture (Poly E) t</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2025-04-21T19:18:57.897Z</modification><creation>2019-03-26T23:42:32Z</creation></dates><accession>S-EPMC6007862</accession><cross_references><pubmed>20112129</pubmed><doi>10.1007/s11095-010-0056-3</doi></cross_references></HashMap>