<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Jia Q</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>Natural Science Basic Research Program of Shaanxi Province</funding><pubmed_abstract>The tumor microenvironment (TME) is variable across tumor types and has diverse effects on malignant progression, based on the type and number of infiltrating stromal cells. In particular, TME effector genes and their competitive endogenous RNA (ceRNA) networks play a critical role in regulating malignant tumor progression. However, the core effector molecules involved in TME modulation of kidney renal papillary cell carcinoma (KIRP) are poorly understood. To address this question, a cohort containing 233 KIRP patients was derived from The Cancer Genome Atlas (TCGA) database, and the data were processed using the ESTIMATE algorithm. We further evaluated the relationship between immune scores (ISs) and stromal scores (SSs) and disease progression and found that high SSs were associated with</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>740051</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8815460</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Anti-Tumor Role of CAMK2B in Remodeling the Stromal Microenvironment and Inhibiting Proliferation in Papillary Renal Cell Carcinoma.</pubmed_title><pmcid>PMC8815460</pmcid><pubmed_authors>Jia Q</pubmed_authors><pubmed_authors>Liao X</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Xu B</pubmed_authors><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Bian G</pubmed_authors><pubmed_authors>Song Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anti-Tumor Role of CAMK2B in Remodeling the Stromal Microenvironment and Inhibiting Proliferation in Papillary Renal Cell Carcinoma.</name><description>The tumor microenvironment (TME) is variable across tumor types and has diverse effects on malignant progression, based on the type and number of infiltrating stromal cells. In particular, TME effector genes and their competitive endogenous RNA (ceRNA) networks play a critical role in regulating malignant tumor progression. However, the core effector molecules involved in TME modulation of kidney renal papillary cell carcinoma (KIRP) are poorly understood. To address this question, a cohort containing 233 KIRP patients was derived from The Cancer Genome Atlas (TCGA) database, and the data were processed using the ESTIMATE algorithm. We further evaluated the relationship between immune scores (ISs) and stromal scores (SSs) and disease progression and found that high SSs were associated with</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-18T17:09:01.642Z</modification><creation>2025-04-07T04:44:15.543Z</creation></dates><accession>S-EPMC8815460</accession><cross_references><pubmed>35127542</pubmed><doi>10.3389/fonc.2022.740051</doi></cross_references></HashMap>