<HashMap><database>biostudies-literature</database><scores/><additional><submitter>de Souza AM</submitter><funding>São Paulo Research Foundation</funding><funding>GE Healthcare</funding><pagination>2715</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9786563</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Breast tumor inflammation is an immunological process that occurs mainly by mediation of Tumor-Associated Macrophages (TAM). Aiming for a specific measurement of tumor inflammation, the current study evaluated the potential of Positron Emission Tomography (PET) imaging with [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 to evaluate tumor inflammation in a mammary tumor animal model.&lt;h4>Methods&lt;/h4>Female Balb/C mice were inoculated with 4T1 cells. The PET imaging with [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 and [&lt;sup>18&lt;/sup>F]FDG was acquired 3 days, 1 week, and 2 weeks after cell inoculation.&lt;h4>Results&lt;/h4>The [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 tumor uptake increased from 3 days to 1 week, and decreased at 2 weeks after cell inoculation, as opposed to the [&lt;sup>18&lt;/sup>F]FDG uptake, w</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Potential of [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 PET Imaging for Evaluating Tumor Inflammation: A Murine Mammary Tumor Model.</pubmed_title><pmcid>PMC9786563</pmcid><funding_grant_id>104.441</funding_grant_id><funding_grant_id>12496139131 and 104.441</funding_grant_id><funding_grant_id>12496139131</funding_grant_id><funding_grant_id>19/15654-2</funding_grant_id><pubmed_authors>de Paula Faria D</pubmed_authors><pubmed_authors>Real CC</pubmed_authors><pubmed_authors>Sapienza MT</pubmed_authors><pubmed_authors>de Souza AM</pubmed_authors><pubmed_authors>Estessi de Souza L</pubmed_authors><pubmed_authors>Navarro Marques FL</pubmed_authors><pubmed_authors>Junqueira MS</pubmed_authors><pubmed_authors>Buchpiguel CA</pubmed_authors><pubmed_authors>Chammas R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Potential of [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 PET Imaging for Evaluating Tumor Inflammation: A Murine Mammary Tumor Model.</name><description>&lt;h4>Background&lt;/h4>Breast tumor inflammation is an immunological process that occurs mainly by mediation of Tumor-Associated Macrophages (TAM). Aiming for a specific measurement of tumor inflammation, the current study evaluated the potential of Positron Emission Tomography (PET) imaging with [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 to evaluate tumor inflammation in a mammary tumor animal model.&lt;h4>Methods&lt;/h4>Female Balb/C mice were inoculated with 4T1 cells. The PET imaging with [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 and [&lt;sup>18&lt;/sup>F]FDG was acquired 3 days, 1 week, and 2 weeks after cell inoculation.&lt;h4>Results&lt;/h4>The [&lt;sup>11&lt;/sup>C](&lt;i>R&lt;/i>)-PK11195 tumor uptake increased from 3 days to 1 week, and decreased at 2 weeks after cell inoculation, as opposed to the [&lt;sup>18&lt;/sup>F]FDG uptake, w</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-08-28T03:07:17.442Z</modification><creation>2025-04-07T02:58:17.972Z</creation></dates><accession>S-EPMC9786563</accession><cross_references><pubmed>36559209</pubmed><doi>10.3390/pharmaceutics14122715</doi></cross_references></HashMap>