Abstract 26P
Background
Young breast cancer (BC) patients frequently exhibit aggressive characteristics such as high rates of metastases, high immune evasion and intricate therapy resistance. Recently, this group has demonstrated elevated resistance to PD-1/PD-L1 immune checkpoint inhibitors, prompting concerns regarding the effectiveness of existing treatment approaches. So, understanding the molecular processes underlying these patients' resistance to immunotherapy is critical for improving treatment selection and effectiveness. Long non-coding RNAs (LncRNAs) has recently been reported to act as immuno-modulators of BC cells. Consequently, making them potentially useful as cancer-immune biomarkers for determining treatment regimen. In BC, these lncRNAs were found to oncogenic lncRNAs and have a positive correlation with increased expression of PD-L1. Thus, our goal is to explore if these lncRNAs can serve as a non-invasive biomarker for the identification of young BC patients who are more likely to be responsive to PD-L1 inhibitors, hence assisting in the formulation of treatment decisions.
Methods
Breast tissues and serum samples were obtained from BC patients (n=40). Total RNA was isolated and extracted from serum and tissue samples and quantified via qRT-PCR. Bioinformatics and survival analysis data regarding breast cancer were gathered and retrieved from the TCGA database and by using KM plotter respectively (https://kmplot.com/analysis/).
Results
PD-L1, CCAT-1 and HEIH expression levels were considerably higher in BC tissues and serum. Young BC patients had significantly greater expression of lncRNAs compared to older patients in tissues and serum samples. TNM plot showed significant upregulation of CCAT1 in basal subtype and significant downregulation of HEIH in basal subtype. In Basal BC patients, survival study using the Kaplan-Meier plotter showed that CCAT-1 overexpression was related with lower overall survival. In contrast, HEIH overexpression was associated with higher overall survival rates.
Conclusions
CCAT1 and HEIH are novel non-invasive biomarkers that could serve as valuable predictive biomarkers to guide treatment decisions in this high-risk patient population.
Legal entity responsible for the study
The authors.
Funding
L'Oreal-UNESCO for women in science.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
44P - Machine learning-based prediction of survival in patients with metastatic renal cell carcinoma receiving first-line immunotherapy
Presenter: Ahmed Elgebaly
Session: Poster Display session
Resources:
Abstract
45P - Gut microbiome signatures for exploring the correlation between gut microbiome and immune therapy response using machine learning approach
Presenter: Han Li
Session: Poster Display session
Resources:
Abstract
46P - Abnormal gut microbiota may cause PD-1 inhibitor-related cardiotoxicity via suppressing regulatory T cells
Presenter: Zeeshan Afzal
Session: Poster Display session
Resources:
Abstract
47P - Correlation of clinical, genetic and transcriptomic traits with PD-L1 positivity in TNBC patients
Presenter: Anita Semertzidou
Session: Poster Display session
Resources:
Abstract
48P - The A2AR antagonist inupadenant promotes humoral responses in preclinical models
Presenter: Paola Tieppo
Session: Poster Display session
Resources:
Abstract
49P - Highly potent novel armoured IL13Ra2 CAR T cell targeting glioblastoma
Presenter: Maurizio Mangolini
Session: Poster Display session
Resources:
Abstract
50P - Phase I trial of P-MUC1C-ALLO1 allogeneic CAR-T cells in advanced epithelial malignancies
Presenter: David Oh
Session: Poster Display session
Resources:
Abstract
51P - Unlocking CAR-T cell potential: Lipid metabolites in overcoming exhaustion in ovarian cancer
Presenter: Xiangyu Chang
Session: Poster Display session
Resources:
Abstract
52P - Tumor-targeted cytokine release by genetically-engineered myeloid cells rescues CAR-T activity and engages endogenous T cells against high-grade glioma in mouse models
Presenter: Federico Rossari
Session: Poster Display session
Resources:
Abstract
53P - Novel ex-vivo manufacturing of transiently expressed armoured CAR T cells for glioblastoma
Presenter: Saket Srivastava
Session: Poster Display session
Resources:
Abstract