AI Article Synopsis

  • Cholangiocarcinoma (CCA) is a type of liver cancer with rising cases and a poor outlook, prompting research into immune checkpoint inhibitors (ICIs) to improve treatment outcomes.
  • A pilot study examined 19 immune checkpoints in CCA patients, finding that certain markers like IDO1 and PD-L1 were associated with worse survival rates, highlighting their potential as prognostic indicators.
  • The research also identified other immune modulators that work with PD-L1 and are linked to aggressive cancer traits, suggesting that targeting these molecules could improve therapies for CCA.

Article Abstract

Cholangiocarcinoma (CCA) is a hepatobiliary malignancy associated with steadily increasing incidence and poor prognosis. Ongoing clinical trials are assessing the effectiveness and safety of a few immune checkpoint inhibitors (ICIs) in CCA patients. However, these ICI treatments as monotherapies may be effective for a proportion of patients with CCA. The prevalence and distribution of other immune checkpoints (ICs) in CCA remain unclear. In this pilot study, we screened databases of CCA patients for the expression of 19 ICs and assessed the prognostic significance of these ICs in CCA patients. Notably, expression of immune modulator IDO1 and PD-L1 were linked with poor overall survival, while FASLG and NT5E were related to both worse overall survival and progression-free survival. We also identified immune modulators IDO1, FASLG, CD80, HAVCR2, NT5E, CTLA-4, LGALS9, VTCN1 and TNFRSF14 that synergized with PD-L1 and correlated with worse patient outcomes. In vitro studies revealed that the expression of ICs was closely linked with aggressive CCA subpopulations, such as cancer stem cells and cells undergoing TGF-β and TNF-α-mediated epithelial-to-mesenchymal transition. These findings suggest that the aforementioned IC molecules may serve as potential prognostic biomarkers and drug targets in CCA patients, leading to lasting and durable treatment outcomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159105PMC
http://dx.doi.org/10.3390/jcm10102191DOI Listing

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