<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Watabe T</submitter><funding>Japan Science and Technology Agency</funding><pagination>9434</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9409053</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(16)</volume><pubmed_abstract>Astatine (&lt;sup>211&lt;/sup>At) is an alpha-emitter with a better treatment efficacy against differentiated thyroid cancer compared with iodine (&lt;sup>131&lt;/sup>I), a conventional beta-emitter. However, its therapeutic comparison has not been fully evaluated. In this study, we compared the therapeutic effect between [&lt;sup>211&lt;/sup>At]NaAt and [&lt;sup>131&lt;/sup>I]NaI. In vitro analysis of a double-stranded DNA break (DSB) and colony formation assay were performed using K1-NIS cells. The therapeutic effect was compared using K1-NIS xenograft mice administered with [&lt;sup>211&lt;/sup>At]NaAt (0.4 MBq (n = 7), 0.8 MBq (n = 9), and 1.2 MBq (n = 4)), and [&lt;sup>131&lt;/sup>I]NaI (1 MBq (n = 4), 3 MBq (n = 4), and 8 MBq (n = 4)). The [&lt;sup>211&lt;/sup>At]NaAt induced higher numbers of DSBs and had a more reduced col</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Comparison of the Therapeutic Effects of [&lt;sup>211&lt;/sup>At]NaAt and [&lt;sup>131&lt;/sup>I]NaI in an NIS-Expressing Thyroid Cancer Mouse Model.</pubmed_title><pmcid>PMC9409053</pmcid><funding_grant_id>JPMJOP1721</funding_grant_id><pubmed_authors>Haba H</pubmed_authors><pubmed_authors>Shimosegawa E</pubmed_authors><pubmed_authors>Toyoshima A</pubmed_authors><pubmed_authors>Nakano T</pubmed_authors><pubmed_authors>Kaneda-Nakashima K</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Sato T</pubmed_authors><pubmed_authors>Watabe T</pubmed_authors><pubmed_authors>Shinohara A</pubmed_authors><pubmed_authors>Hatazawa J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Ooe K</pubmed_authors><pubmed_authors>Shirakami Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparison of the Therapeutic Effects of [&lt;sup>211&lt;/sup>At]NaAt and [&lt;sup>131&lt;/sup>I]NaI in an NIS-Expressing Thyroid Cancer Mouse Model.</name><description>Astatine (&lt;sup>211&lt;/sup>At) is an alpha-emitter with a better treatment efficacy against differentiated thyroid cancer compared with iodine (&lt;sup>131&lt;/sup>I), a conventional beta-emitter. However, its therapeutic comparison has not been fully evaluated. In this study, we compared the therapeutic effect between [&lt;sup>211&lt;/sup>At]NaAt and [&lt;sup>131&lt;/sup>I]NaI. In vitro analysis of a double-stranded DNA break (DSB) and colony formation assay were performed using K1-NIS cells. The therapeutic effect was compared using K1-NIS xenograft mice administered with [&lt;sup>211&lt;/sup>At]NaAt (0.4 MBq (n = 7), 0.8 MBq (n = 9), and 1.2 MBq (n = 4)), and [&lt;sup>131&lt;/sup>I]NaI (1 MBq (n = 4), 3 MBq (n = 4), and 8 MBq (n = 4)). The [&lt;sup>211&lt;/sup>At]NaAt induced higher numbers of DSBs and had a more reduced col</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-27T02:29:39.503Z</modification><creation>2025-02-19T04:38:09.94Z</creation></dates><accession>S-EPMC9409053</accession><cross_references><pubmed>36012698</pubmed><doi>10.3390/ijms23169434</doi></cross_references></HashMap>