bioRxiv Science⌕ Search

bioRxiv · 10.1101/2024.08.16.608025

Machine learning based identification of candidate miRNA biomarkers for micro-invasive breast cancer diagnosis

Abstract

Abstract PurposeEarly detection of cancer can be done by analyzing miRNA expression patterns. miRNAs play a significant role in biological processes, and they have been identified as one of the major biomarkers in cancer. miRNAs can also be detected in human blood (micro-invasive way of sample collection), which makes the diagnostic procedure much less stressful for the patients. In this article, we emphasize on identification of miRNAs as biomarkers (collected from blood sample) that are associated with breast cancer. MethodsIn this investigation we use three breast cancer data sets, obtained from blood samples. A combination of multiple feature selection and classification models is used to classify normal vs cancer samples. In the first stage, the significant miRNAs associated with cancer were selected by (a) classifier assigned weights and (b) feature selection algorithms. In the second stage, we apply multiple classifiers to observe the diagnostic capability of the selected miRNAs for consideration as potential biomarkers. ResultsOur miRNA selection stage identified ten miRNAs, which were subsequently analysed using multiple classifiers for their ability to distinguish between normal and cancerous cases. The performance is examined using a 5-fold cross validation technique using multiple measures such as precision, recall, F1-score, and accuracy. We also use a confusion matrix to evaluate the performance of the selected miRNAs. For two out of three datasets, we achieve satisfactory performance in terms of normal vs cancer classification. ConclusionWe observe that high expression levels of miRNA is relatively more important than the sample size, for effective blood-based diagnosis of breast cancer. The novelty of our investigation lies in combining three aspects viz., blood-based breast cancer diagnosis, use of multiple ML based feature selection algorithms to identify the miRNAs associated with breast cancer, evaluating them using various classifiers and the robustness of these ML models in feature selection and classification.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Pal, J. K., Rami, B. R.. 2024-08-19. Machine learning based identification of candidate miRNA biomarkers for micro-invasive breast cancer diagnosis. https://doi.org/10.1101/2024.08.16.608025

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Epigenetic progression of pancreatic cancer to aggressive subtypes involves alternate routes of lineage reprogramming in subtype-intermediate progenitor cells

Pancreatic ductal adenocarcinoma (PDAC) progression involves malignant cell state plasticity. Epigenetic changes underlie this plasticity, yet the PDAC cis-regulatory landscape remains understudied. To address this, we profiled 33 primary tumors and 7 metastases from 39 patients with single-cell ATAC-seq, paired with 10 single-cell RNA-seq profiles. We found that epigenetic GATA6+/KRT17+ co-accessibility identifies a classical-basal subtype-intermediate progenitor state (SIP) associated with better clinical outcomes. SIP cells display limited epigenetic reprogramming from premalignant epithelium and retain gastric-intestinal differentiation reminiscent of neoplastic precursors. Lineages without GATA6+/KRT17+ co-accessibility exhibit greater lineage and epithelial-mesenchymal plasticity. Classical PDACs that repress basal gene accessibility activate neural-like progenitor (NRP) and tuft lineage enhancers, whereas basal committed tumors display esophageal transdifferentiation. Compared to SIP, classical-NRP and basal committed tumors have poorer outcomes, and show distinct PD-1/PD-L1 immune proteomic phenotypes and prognostic myofibroblast epigenetic states, respectively. Our work reveals links between lineage reprogramming, EMT, and epigenetic progression in human PDAC.

cancer biology↗

Tissue resident CD4+ memory T-cells mark response to immune checkpoint inhibition in high-grade glioma

Background: Immune checkpoint inhibitors (ICI) are efficacious in many solid tumors, but response in glioma is restricted to a small subgroup. The determinants of response and resistance to ICI remain poorly understood. Methods: Here we exploit a syngeneic hypermutated high-grade glioma model with dichotomous response to combined PD-1 and CTLA-4 inhibition to unravel determinants of tumor-infiltrating T-cells driving response. Tumor-infiltrating T-cells from ICI-responsive and non-responsive tumors were analyzed by single-cell RNA and T-cell receptor sequencing and tumor-reactive T-cell receptor clonotypes were functionally validated to characterize their transcriptional phenotypes. We verify our findings in IDH1 wildtype glioblastoma patients treated with neoadjuvant pembrolizumab. Results: ICI response was associated with intratumoral clonal expansion of tumor-reactive cytotoxic T-cells and increased infiltration of CXCR6+ CD4+ tissue resident memory T-cells (Trm). CD4 stem-like memory T-cells in responding tumors demonstrated elevated interferon responses, following trajectories toward clonally expanded Trm, versus trajectories toward exhaustion in non-responsive tumors. In responsive tumors, CD4+ Trm interacted with infiltrating CXCR3+ tumor-reactive and clonally expanded, yet transcriptionally versatile cytotoxic T-cells. Probing the post neoadjuvant ICI high-grade glioma patient tissue dataset, we confirmed increased CXCR6 expression in CD4+ T cells and the association of CD4+ Trm with prolonged overall survival. Conclusion: These findings identify CD4 tissue-resident memory T-cells as determinants of ICI response in IDH1 wildtype high-grade glioma and warrant their further investigation to improve immunotherapy outcomes.

cancer biology↗

Low-dose doxorubicin drives caveolin-1 depended re-epithelialization of breast cancer cells as a mechanism of cancer plasticity

Breast cancer progression is driven by dynamic changes in epithelial plasticity, membrane organization, and intracellular signaling, yet the effects of sustained low-dose chemotherapy on these processes remain poorly understood. Here, we investigated the impact of prolonged low-dose doxorubicin on membrane remodeling, epithelial phenotype, membrane-associated Ras lipid-anchor localization, and autophagy in mesenchymal-like MDA-MB-231 breast cancer cells. Low-dose doxorubicin significantly increased Caveolin-1 expression and enhanced E-cadherin protein levels, accompanied by a transition toward a more compact epithelial-like morphology with increased cell-cell contacts. Live-cell imaging demonstrated a significant reduction in the membrane-to-cytoplasm fluorescence ratio of the lipid-anchored GFP-tH probe, indicating redistribution from the plasma membrane to the cytoplasm following treatment. Analysis of autophagy-related proteins revealed decreased LC3-I together with increased LC3-II, ATG5, and p62 expression, consistent with autophagosome accumulation and impaired autophagic flux. Collectively, our findings demonstrate that low-dose doxorubicin promotes extensive remodeling of plasma membrane organization, epithelial plasticity, membrane-associated lipid-anchor localization, and autophagy. This integrated response reveals previously unrecognized links between membrane architecture, Ras membrane association, and autophagy during phenotypic reprogramming of breast cancer cells, providing mechanistic insight into cellular adaptations elicited by sub-cytotoxic doxorubicin exposure.

cancer biology↗