Bladder Cancer Cell-Intrinsic PD-L1 Signals Affecting Virulence and Treatment Resistance

Abstract

Recent approvals of five distinct immunotherapy agents for BC have revolutionized the treatment of late-stage disease. Nevertheless, complete clinical responses to these immunotherapy agents are achieved in only a minority of patients and there are no unambiguous and reliable biomarkers to guide treatment selection. Thus, we need a greatly improved understanding of BC immunotherapy responses to help improve its efficacy and to develop useful treatment response biomarkers. We study novel BC-intrinsic PD-L1 signals that likely mediate important immunopathologic roles in BC, including mediating resistance to FDA-approved immunotherapies such as anti-PD-L1. These treatment response mechanisms and related biomarkers that we study here likely will also be useful in treatment applications in addition to immunotherapy and could apply to cancers in addition to BC.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2021
Accession Number
AD1156778

Entities

People

  • Tyler J Curiel

Organizations

  • University of Texas at San Antonio

Tags

DTIC Thesaurus Topics

  • Autophagy
  • Biological Markers
  • Biomedical Research
  • Bladder Cancer
  • Blood
  • Cancer
  • Cell Count
  • Cell Line
  • Cells
  • Chemotherapy
  • Combination Therapy
  • Immunotherapy
  • Inhibitors
  • Medical Personnel
  • Neoplasms
  • Ovarian Cancer
  • Proteins

Fields of Study

  • Biology
  • Medicine

Readers

  • Neurodegenerative Parkinson's Disease and Rickettsial Disease handbook, including the data level of dopamine, BC, neurons, and PD.
  • Oncology

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech