<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE280nnn/GSE280469/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE280469</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>P5CS regulates translation by functioning as non-canonical RBP [Ribo-seq]</name><description>P5CS is the rate-limiting enzyme in the proline biosynthetic pathway, while whether P5CS mediates function beyond enzyme activity remains completely unknown. Here, we reveal that P5CS functions as a non-canonical RNA-binding protein and inhibits the growth and metastasis of cancer cells by suppressing translation initiation in an enzyme activity-independent manner. To explore the underlying mechanism of P5CS in translation regulation, Ribo-seq, RIP-seq and LACE-seq were performed to investigate the downstream targets of P5CS.</description><dates><publication>2026/06/09</publication></dates><accession>GSE280469</accession><cross_references><GSM>GSM8598397</GSM><GSM>GSM8598398</GSM><GSM>GSM8598393</GSM><GSM>GSM8598394</GSM><GSM>GSM8598395</GSM><GSM>GSM8598396</GSM><GPL>24676</GPL><GSE>280469</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>