Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatment with anti-programmed death receptor 1 (PD-1) has been widely used in recurrent or metastatic tumors. However, integrated studies considering CD274 and PDCD1LG2 across cancers remain limited.Materials and Methods: Differences in expression levels of CD274 and PDCD1LG2 were analyzed in diverse cancer types using The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases. The clinical information and matched expression profiles of TCGA patients were obtained to determine the prognostic value of CD274 and PDCD1LG2. Moreover, correlations between CD274 and PDCD1LG2 and the immune signature were analyzed by exploring the TIM...
Introduction Several studies have shown clinical outcomes data that support the use of CD274 (PD-L1)...
Immune checkpoint blockade targeting PD-1 (PDCD1)/PD-L1 (CD274) is increasingly used for multiple ca...
Background The effects of non-amplification short variant (SV) mutations in CD274 (programmed death-...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Aim The prognostic role of CD274 (programmed cell death ligand 1 (PD-L1)) overexpression has been ex...
Objective: This study aimed to identify the programmed death ligand-1 (PDL1, also termed as CD274) a...
Introduction Several studies have shown clinical outcomes data that support the use of CD274 (PD-L1)...
Immune checkpoint blockade targeting PD-1 (PDCD1)/PD-L1 (CD274) is increasingly used for multiple ca...
Background The effects of non-amplification short variant (SV) mutations in CD274 (programmed death-...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Background: Disorders of CD274 and PDCD1LG2 contribute to immune escape in human cancers, and treatm...
Aim The prognostic role of CD274 (programmed cell death ligand 1 (PD-L1)) overexpression has been ex...
Objective: This study aimed to identify the programmed death ligand-1 (PDL1, also termed as CD274) a...
Introduction Several studies have shown clinical outcomes data that support the use of CD274 (PD-L1)...
Immune checkpoint blockade targeting PD-1 (PDCD1)/PD-L1 (CD274) is increasingly used for multiple ca...
Background The effects of non-amplification short variant (SV) mutations in CD274 (programmed death-...