<HashMap><database>EVA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1435562/MP-MGH-U3_somatic_standardized_fixed.vcf.gz.csi</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1435562/UCSD-MGH-U3_somatic_standardized_fixed.vcf.gz</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1435562/UCSD-MGH-U3_somatic_standardized_fixed.vcf.gz.csi</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1435562/MP-MGH-U3_somatic_standardized_fixed.vcf.gz</Vcf><Other>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1435562/MP-MGH-U3_somatic_standardized_fixed.vcf.csi</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1435562/UCSD-MGH-U3_somatic_standardized_fixed.vcf.csi</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><dataset_type>Exome Sequencing</dataset_type><omics_type>Genomics</omics_type><submitter>Shenzhen University, South China Hospital</submitter><instrument_platform>Illumina</instrument_platform><species>Homo Sapiens</species><full_dataset_link>https://www.ebi.ac.uk/eva/?eva-study=PRJNA1435562</full_dataset_link><repository>EVA</repository></additional><is_claimable>false</is_claimable><name>Recurrence in the chemotherapy regimen of bladder carcinoma originates from quiescent epidermoid-like cells</name><description>Cancer relapse upon chemotherapy remains the primary challenge in cancer treatment. By integrating high-resolution CRISPR/Cas9-based evolving lineage tracing with single-cell RNA sequencing in mice, we tracked the evolution of bladder carcinoma in the presence or absence of chemotherapy. We found that a cell population exhibiting an epidermoid-like cell state was able to survive chemotherapy. These epidermoid-like cells left the quiescent state to initiate relapse, generating histologically distinct tumors through different evolutionary routes involving specific transcriptional changes. The plasticity of epidermoid-like cells and alterations in plasticity patterns during evolution have shaped the phenotypes of relapsed tumors. Integrated analyses revealed that Insulin-like growth factor-binding protein 5 was a key co-regulator of aggressive progression and squamous features in bladder carcinoma. Impeding Insulin-like growth factor-binding protein 5 expression suppressed the chemoresistance and malignant behaviors of relapsed tumors. Our study deciphers key events and evolutionary dynamics during the natural progression and recurrence of bladder carcinoma. It offers a viable therapeutic approach to overcome the refractoriness of relapsed bladder carcinoma to conventional chemotherapy.</description><dates><publication>2026-03-12</publication></dates><accession>PRJNA1435562</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>