<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(5)</volume><submitter>Wei X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Autophagy was a significant catabolic process which played a critical role in the maintenance of cellular homeostasis and viability in a stressed state. The dysregulation of autophagy was correlated with various diseases. The aim of our study was to develop a prognostic signature for papillary renal cell carcinoma (RCC).&lt;h4>Methods&lt;/h4>First, 40 differently expressed genes related with autophagy (ARGs) were examined via high-throughput sequencing and large-scale databases. Then, functional enrichment analysis was performed to explore the biological attributes of these ARGs. The Cox proportional hazard regression hinted that four ARGs (&lt;i>P4HB&lt;/i>, &lt;i>BIRC5&lt;/i>, &lt;i>NGR1&lt;/i> and &lt;i>PRKN&lt;/i>) were significantly correlated with overall survival (OS). Thus, we got genes with prognostic value. Finally, a prognostic index (PI) was constructed.&lt;h4>Results&lt;/h4>After identifying the 4 ARGs, we profiled our risk signature. Based on the PI we developed, papillary RCC patients were stratified into high-risk and low-risk groups. High-risk patients had significant shorter OS than low-risk patients (P&lt;0.001) and the mortality of high scoring patients was higher than low scoring patients. Additionally, we explored the relationship between the 4 ARGs and clinical parameters and found that the expression of &lt;i>P4HB&lt;/i>, &lt;i>BIRC5&lt;/i> and &lt;i>NGR1&lt;/i> was correlated with clinicopathological features.&lt;h4>Conclusions&lt;/h4>Our study suggested that the four-gene signature was an independent prognostic factor which could act as a novel indicator for the prognosis of papillary RCC.</pubmed_abstract><journal>Translational andrology and urology</journal><pagination>1945-1956</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7658136</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of an independent autophagy-gene prognostic index for papillary renal cell carcinoma.</pubmed_title><pmcid>PMC7658136</pmcid><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Ren X</pubmed_authors><pubmed_authors>Ji C</pubmed_authors><pubmed_authors>Song N</pubmed_authors><pubmed_authors>Wei X</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Qin C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of an independent autophagy-gene prognostic index for papillary renal cell carcinoma.</name><description>&lt;h4>Background&lt;/h4>Autophagy was a significant catabolic process which played a critical role in the maintenance of cellular homeostasis and viability in a stressed state. The dysregulation of autophagy was correlated with various diseases. The aim of our study was to develop a prognostic signature for papillary renal cell carcinoma (RCC).&lt;h4>Methods&lt;/h4>First, 40 differently expressed genes related with autophagy (ARGs) were examined via high-throughput sequencing and large-scale databases. Then, functional enrichment analysis was performed to explore the biological attributes of these ARGs. The Cox proportional hazard regression hinted that four ARGs (&lt;i>P4HB&lt;/i>, &lt;i>BIRC5&lt;/i>, &lt;i>NGR1&lt;/i> and &lt;i>PRKN&lt;/i>) were significantly correlated with overall survival (OS). Thus, we got genes with prognostic value. Finally, a prognostic index (PI) was constructed.&lt;h4>Results&lt;/h4>After identifying the 4 ARGs, we profiled our risk signature. Based on the PI we developed, papillary RCC patients were stratified into high-risk and low-risk groups. High-risk patients had significant shorter OS than low-risk patients (P&lt;0.001) and the mortality of high scoring patients was higher than low scoring patients. Additionally, we explored the relationship between the 4 ARGs and clinical parameters and found that the expression of &lt;i>P4HB&lt;/i>, &lt;i>BIRC5&lt;/i> and &lt;i>NGR1&lt;/i> was correlated with clinicopathological features.&lt;h4>Conclusions&lt;/h4>Our study suggested that the four-gene signature was an independent prognostic factor which could act as a novel indicator for the prognosis of papillary RCC.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2026-06-12T09:53:44.384Z</modification><creation>2025-04-19T23:41:02.088Z</creation></dates><accession>S-EPMC7658136</accession><cross_references><pubmed>33209659</pubmed><doi>10.21037/tau-20-906</doi></cross_references></HashMap>