<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Shim S</submitter><funding>National Research Foundation of Korea</funding><funding>Korea Food Research Institute</funding><pubmed_abstract>IL-32 plays a contradictory role such as tumor proliferation or suppressor in cancer development depending on the cancer type. In most cancers, it was found that the high expression of IL-32 was associated with more proliferative and progression of cancer. However, studying the isoforms of IL-32 cytokine has placed its paradoxical role into a wide range of functions based on its dominant isoform and surrounding environment. IL-32β, for example, was found mostly in different types of cancer and associated with cancer expansion. This observation is legitimate since cancer exhibits some hypoxic environment and IL-32β was known to be induced under hypoxic conditions. However, IL-32θ interacts directly with protein kinase C-δ reducing NF-κB and STAT3 levels to inhibit epithelial-mesenchymal tra</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>837590</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8913503</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Paradoxical Effect of Interleukin-32 Isoforms on Cancer.</pubmed_title><pmcid>PMC8913503</pmcid><pubmed_authors>Shim S</pubmed_authors><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Kim SY</pubmed_authors><pubmed_authors>Jhun H</pubmed_authors><pubmed_authors>Kim YG</pubmed_authors><pubmed_authors>Hwang J</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Nguyen TT</pubmed_authors><pubmed_authors>Yeom SC</pubmed_authors><pubmed_authors>Taitt AS</pubmed_authors><pubmed_authors>Park HY</pubmed_authors><pubmed_authors>Lee Y</pubmed_authors><pubmed_authors>Hisham Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Paradoxical Effect of Interleukin-32 Isoforms on Cancer.</name><description>IL-32 plays a contradictory role such as tumor proliferation or suppressor in cancer development depending on the cancer type. In most cancers, it was found that the high expression of IL-32 was associated with more proliferative and progression of cancer. However, studying the isoforms of IL-32 cytokine has placed its paradoxical role into a wide range of functions based on its dominant isoform and surrounding environment. IL-32β, for example, was found mostly in different types of cancer and associated with cancer expansion. This observation is legitimate since cancer exhibits some hypoxic environment and IL-32β was known to be induced under hypoxic conditions. However, IL-32θ interacts directly with protein kinase C-δ reducing NF-κB and STAT3 levels to inhibit epithelial-mesenchymal tra</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T07:55:05.291Z</modification><creation>2025-04-04T07:55:05.291Z</creation></dates><accession>S-EPMC8913503</accession><cross_references><pubmed>35281008</pubmed><doi>10.3389/fimmu.2022.837590</doi></cross_references></HashMap>