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Updated: Jul 10, 2025

Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
[Relationship between PD-L1 expression and tumor stem cell marker CD44 as a promising basis for the development of
T N Sotnikova1,2, T V Polushkina1,3, N V Danilova3
1I.V. Davydovsky City Clinical Hospital, Moscow, Russia.
Abstract:
Immunotherapy of malignant tumors is a rapidly developing area of oncology. PD-1 is a receptor expressed by activated T-lymphocytes. As a result of its interaction with the ligand (PD-L1 or PD-L2), the activity of T-lymphocytes is inhibited and their apoptosis occurs. Drugs that inhibit the interaction of PD-1 with ligands have an immunostimulatory effect and are effective in the treatment of many types of neoplasms: melanoma, lung cancer, bladder cancer, stomach cancer, various lymphomas, etc. However, response to this treatment is observed only in a narrow cohort of patients. To increase the effectiveness of immunotherapy, combined preparations and nanoparticles are being developed and created to enhance the effect of PD-L1 inhibitors, and containing hyaluronic acid as a ligand for the CD44 protein, which is expressed in many human tumors. However, the issue of co-expression of CD44 and PD-L1 remains poorly understood. This review is devoted to describing the features of co-expression and the mechanisms of interaction between CD44 and PD-L1. Promising directions for the development of new approaches to the immunotherapy of malignant tumors are presented.
Insights
Immunotherapy using PD-1 inhibitors shows promise for cancer treatment but benefits a limited patient group. This review explores the co-expression of CD44 and PD-L1 to improve immunotherapy effectiveness.
Area of Science:
- Oncology
- Immunology
- Nanotechnology
Background:
- Immunotherapy targeting the PD-1/PD-L1 pathway is a growing field in oncology.
- PD-1 receptor interaction with PD-L1/PD-L2 ligands inhibits T-lymphocyte activity and promotes apoptosis.
- Current PD-1 inhibitors are effective for various cancers but benefit only a subset of patients.
Conclusions:
- Understanding CD44 and PD-L1 co-expression is crucial for advancing cancer immunotherapy.
- Combined approaches, including targeted nanoparticles, hold promise for increasing treatment efficacy.
- Further research into CD44-PD-L1 interactions can lead to novel therapeutic strategies for malignant tumors.
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