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
125P - Enhancing the efficacy of neoantigen tumor vaccines in melanoma treatment through different administration times
Presenter: Kai Xiao
Session: Poster Display session
Resources:
Abstract
126P - Combination of oncolytic viruses, radiation therapy, and immune checkpoint inhibitor treatment in a breast cancer model
Presenter: Olga Bezborodova
Session: Poster Display session
Resources:
Abstract
127P - Combining chemotherapy and checkpoint inhibitors with an engineered oncolytic adenovirus encoding a human vIL-2 cytokine to treat pancreatic ductal adenocarcinoma
Presenter: Nea Ojala
Session: Poster Display session
Resources:
Abstract
128P - Non-coding DNA lipid nanoparticles elicit antitumor immune responses and synergize with anti-PDL1 antibodies in mouse models of hepatocellular carcinoma
Presenter: Alba Rodriguez Garcia
Session: Poster Display session
Resources:
Abstract
129P - Computational approaches for enhancing the efficacy of cancer immunotherapy
Presenter: Byungho Lim
Session: Poster Display session
Resources:
Abstract
130P - Neoadjuvant treatment with a bispecific antibody cadonilimab in dMMR/MSI-H locally advanced colorectal cancer: Preliminary results from a phase II trial
Presenter: Caifeng Gong
Session: Poster Display session
Resources:
Abstract
131P - The efficacy and safety of cadonilimab with or without trastuzumab in combination with SOX as first-line (1L) treatment for advanced gastric (G) or gastroesophageal Junction adenocarcinoma (GEJA)
Presenter: Wenhui Yang
Session: Poster Display session
Resources:
Abstract
132P - An open-label, prospective phase II study of cadonilimab in combination with neoadjuvant chemotherapy for patients diagnosed with advanced ovarian cancer (AK104-IIT-003)
Presenter: Jie Tang
Session: Poster Display session
Resources:
Abstract
133P - The efficacy and safety of KN046 combined with axitinib for previously untreated and checkpoint inhibitor treated advanced non-small cell lung cancer: A single-arm, open-label, multicenter phase II clinical trial
Presenter: Li Zhang
Session: Poster Display session
Resources:
Abstract
134P - Intracranial (IC) progression-free survival (PFS) with ivonescimab (Ivo) compared to placebo in the HARMONi-A trial of patients (Pts) with previously treated EGFR mutation-positive (EGFRm+) non-small cell lung cancer (NSCLC)
Presenter: Li Zhang
Session: Poster Display session
Resources:
Abstract