Related Experiment Video
Updated: Mar 19, 2026

07:36
Tumor Transplantation for Assessing the Dynamics of Tumor-Infiltrating CD8+ T Cells in Mice
Published on: June 12, 2021
7.8K
Circulating Tumor Cells (CTC) Are Associated with Defects in Adaptive Immunity in Patients with Inflammatory Breast
11. Department of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA;; 5. Currently at 2nd Department of Oncology, Faculty of Medicine, Comenius University and National Cancer Institute, Bratislava, Slovakia;
Journal of Cancer
|June 22, 2016
Summary
Circulating tumor cells (CTCs) in inflammatory breast cancer patients correlate with altered T-cell immunity. These immune changes may influence tumor spread and metastasis.
Area of Science:
- Oncology
- Immunology
- Breast Cancer Research
Background:
- Circulating tumor cells (CTCs) are key indicators of tumor spread and prognosis in breast cancer.
- Peripheral blood immune cells can create an environment that hinders CTC survival.
- Inflammatory breast cancer (IBC) presents unique challenges in understanding tumor dissemination.
Purpose of the Study:
- To investigate the relationship between circulating tumor cells (CTCs) and T-cell immune profiles in patients with inflammatory breast cancer (IBC).
- To determine if T-cell immunophenotypes and functions correlate with CTC presence and clinical outcomes in IBC.
Main Methods:
- Analysis of 65 IBC patients at MD Anderson Cancer Center.
- Enumeration of CTCs using CellSearch® and assessment of T-cell phenotype/function via flow cytometry on peripheral blood samples.
- Correlation of CTC counts with T-cell data and clinical outcomes prior to chemotherapy initiation.
Main Results:
- CTCs were detected in 61.5% of patients (≥1 CTC) and 32.3% (≥5 CTCs).
- Patients with CTCs exhibited lower percentages of CD3+ and CD4+ T cells, reduced T-cell receptor (TCR)-activated CD8+ T cells producing TNF-α and IFN-γ, and higher T-regulatory cells compared to those without CTCs.
- Multivariate analysis linked CTC presence to tumor grade, stage, and specific T-cell percentages (CD3+, CD4+, TCR-activated CD8+ T cells).
Conclusions:
- Patients with IBC and detectable CTCs show significant abnormalities in adaptive immunity.
- These immune alterations may play a role in promoting tumor cell dissemination and the metastatic cascade.
Related Concept Videos
The Tumor Microenvironment
8.1K
Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
8.1K
Metastasis
6.8K
Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
6.8K
Tumor Immunotherapy
2.1K
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
2.1K

