Abstract 177TiP
Background
In cancer, tumor-secreted factors and surgical stress responses induce the migration of myeloid-derived suppressor cells (MDSC) from the bone marrow to the circulation and tumor microenvironment (TME). Due to severe immunosuppression, this process promotes disease progression and negatively affects treatment outcomes. Limited knowledge exists regarding MDSC in colorectal cancer (CRC). Through the use of flow cytometry and a precise gating strategy, we have identified and quantified 3 classes of MDSC in CRC and confirmed their immunosuppressive capacity. Initial findings show an increase of MDSC. Future investigations will focus on comparing MDSC levels among different CRC stages and examining their spatial distribution in the TME. This research aims to enhance our understanding of how MDSC contribute to tumor cell immune evasion and impact treatment outcomes. End of study: end of 2025.
Trial Design
A cohort of 250 patients with operable CRC have pre- and postoperative blood samples drawn for analysis. Flow cytometry is performed on isolated peripheral blood mononuclear cells. Controls are healthy individuals and patients undergoing surgery for non-malignant disease.
Editorial acknowledgement
Clinical trial identification
Legal entity responsible for the study
Center for Surgical Science, Zealand University Hospital.
Funding
Familien Erichsen’s Mindefond (The Erichsen Family Memorial Fund).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
72P - Role of pyruvate carboxykinase 2 upregulation in group 3 medulloblastoma: Implications for metabolic reprogramming and therapeutic strategies
Presenter: MEDHA GAYATHRI PAI
Session: Cocktail & Poster Display session
Resources:
Abstract
73P - Effect of combination therapy with atezolizumab plus metformin on peripheral immune cells from NSCLC patients
Presenter: Luisa Amato
Session: Cocktail & Poster Display session
Resources:
Abstract
74P - Obesity regulates tumor progression and sensitivity to checkpoint blockade through the diet-microbiota-immunity axis
Presenter: Lysanne Desharnais
Session: Cocktail & Poster Display session
Resources:
Abstract
75P - Possible significance of the proline at position 325 in the recognition of the MX35 epitope of the NaPi2b transporter by monoclonal antibodies
Presenter: Leisan Bulatova
Session: Cocktail & Poster Display session
Resources:
Abstract
76P - Circadian control of neutrophil extracellular trap formation temporally regulates metastatic lung cancer progression
Presenter: Simon Milette
Session: Cocktail & Poster Display session
Resources:
Abstract
78P - Daily rhythmic expression of pro-tumoral programs in NSCLC shape cancer immunity and therapy response
Presenter: Alba de Juan
Session: Cocktail & Poster Display session
Resources:
Abstract
79P - Tumor cell-released autophagosomes (TRAPs) remodel the breast tumor microenvironment by inducing the formation of inflammatory cancer-associated fibroblasts (CAFs)
Presenter: Chengdong Wu
Session: Cocktail & Poster Display session
Resources:
Abstract
80P - Tumor microenvironment (TME) defines prognosis of EGFR-mutant non-small cell lung cancer (NSCLC)
Presenter: Lodovica Zullo
Session: Cocktail & Poster Display session
Resources:
Abstract
81P - Single-cell spatial landscape of NSCLC reveals subtype specific immune features
Presenter: Mark Sorin
Session: Cocktail & Poster Display session
Resources:
Abstract
82P - Tumor cell-released autophagosomes (TRAPs) promote breast cancer lung metastasis by modulating neutrophil extracellular traps formation
Presenter: XIAOHE ZHOU
Session: Cocktail & Poster Display session
Resources:
Abstract