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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">mouse</item><item key="factors"><item><item key="GSM958123"><item key="TREATMENT">co-incubated with PDL1-overexpresssed ID8</item></item></item><item><item key="GSM958123"><item key="TREATMENT">co-incubated with PDL1-overexpresssed ID8</item></item></item><item><item key="GSM958123"><item key="TREATMENT">co-incubated with PDL1-overexpresssed ID8</item></item></item><item><item key="GSM958123"><item key="TREATMENT">co-incubated with PDL1-overexpresssed ID8</item></item></item><item><item key="GSM958127"><item key="TREATMENT">co-incubated with PDL1-depleted ID8</item></item></item><item><item key="GSM958127"><item key="TREATMENT">co-incubated with PDL1-depleted ID8</item></item></item><item><item key="GSM958127"><item key="TREATMENT">co-incubated with PDL1-depleted ID8</item></item></item><item><item key="GSM958127"><item key="TREATMENT">co-incubated with PDL1-depleted ID8</item></item></item></item><item key="id">8635</item><item key="pop_total">0</item><item key="platform">8</item><item key="summary_wrapped">Programmed cell death 1 ligand 1 (PD-L1) is known to suppress immune system and to be an unfavorable prognostic factor in ovarian cancer....</item><item key="geo_gse_id">E-GEOD-39205</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">8</item><item key="tags"><item>cancer</item><item>cell</item><item>genome</item><item>immune system</item><item>ovarian cancer</item><item>peritoneal cavity</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">gene-expression-profiles-of-pd-l1-affected-cd8-t-c</item><item key="geo_id_plat">E-GEOD-39205_A-AFFY-36</item><item key="name">Gene-expression profiles of PD-L1-affected CD8+ T cells</item><item key="created">Nov.24, 2014</item><item key="summary">Programmed cell death 1 ligand 1 (PD-L1) is known to suppress immune system and to be an unfavorable prognostic factor in ovarian cancer. The purpose of this study was to elucidate the function of PD-L1 in peritoneal dissemination. Tumor cell lysis by CTLs was attenuated when PD-L1 on tumor cells was overexpressed and promoted when it was silenced. PD-L1 overexpression also inhibited gathering and degranulation of CTLs. Gene expression profile of mouse CTLs caused by PD-L1-overexpressing ovarian cancer was related to human CTLs exhaustion. In mouse ovarian cancer dissemination models, depleting PD-L1 expression on tumor cells resulted in inhibited tumor growth in the peritoneal cavity and prolonged survival. Restoring immune function by inhibiting immune-suppressive factors such as PD-L1 may be a promising therapeutic strategy for peritoneal dissemination. Genome-wide transcriptional changes in OT-1 mouse CD8+ T cells that were co-incubated with OVA peptide-loaded ID8 mouse ovarian cancer cell lines. CTLs from 4 mice were devided into 2 groups, and co-incubated with PD-L1-overexpressed ID8 or PD-L1-depleted ID8.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-39205</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-39205/samples/</item></data></biogps>
