<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sieminska I</submitter><funding>Horizon 2020 Framework Programme</funding><pagination>862416</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9289201</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>Prostate cancer (PC) is the second most often diagnosed malignancy in men and one of the major causes of cancer death worldwide. Despite genetic predispositions, environmental factors, including a high-fat diet, obesity, a sedentary lifestyle, infections of the prostate, and exposure to chemicals or ionizing radiation, play a crucial role in PC development. Moreover, due to a lack of, or insufficient T-cell infiltration and its immunosuppressive microenvironment, PC is frequently classified as a "cold" tumor. This is related to the absence of tumor-associated antigens, the lack of T-cell activation and their homing into the tumor bed, and the presence of immunological cells with regulatory functions, including myeloid-derived suppressor cells (MDSCs), regulatory T cells (Treg), and tumor-a</pubmed_abstract><journal>Frontiers in oncology</journal><pubmed_title>Myeloid-Derived Suppressor Cells as Key Players and Promising Therapy Targets in Prostate Cancer.</pubmed_title><pmcid>PMC9289201</pmcid><funding_grant_id>GA 777682</funding_grant_id><pubmed_authors>Sieminska I</pubmed_authors><pubmed_authors>Baran J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Myeloid-Derived Suppressor Cells as Key Players and Promising Therapy Targets in Prostate Cancer.</name><description>Prostate cancer (PC) is the second most often diagnosed malignancy in men and one of the major causes of cancer death worldwide. Despite genetic predispositions, environmental factors, including a high-fat diet, obesity, a sedentary lifestyle, infections of the prostate, and exposure to chemicals or ionizing radiation, play a crucial role in PC development. Moreover, due to a lack of, or insufficient T-cell infiltration and its immunosuppressive microenvironment, PC is frequently classified as a "cold" tumor. This is related to the absence of tumor-associated antigens, the lack of T-cell activation and their homing into the tumor bed, and the presence of immunological cells with regulatory functions, including myeloid-derived suppressor cells (MDSCs), regulatory T cells (Treg), and tumor-a</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-29T10:40:19.491Z</modification><creation>2025-02-19T02:43:37.984Z</creation></dates><accession>S-EPMC9289201</accession><cross_references><pubmed>35860573</pubmed><doi>10.3389/fonc.2022.862416</doi></cross_references></HashMap>