<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Opperman RM</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Canada Graduate Scholarships – Master’s program</funding><funding>Research Manitoba’s CFI Matching Fund</funding><funding>Lotte and John Hecht Memorial Foundation</funding><funding>Breast Cancer Canada</funding><funding>Research Manitoba masters studentship</funding><funding>Canada Foundation for Innovation</funding><funding>Canada Research Chairs</funding><pubmed_abstract>Doxorubicin is an effective treatment for breast cancer, but drug resistance poses a significant challenge. Emerging regulators of drug resistance include microRNAs, small non-coding RNAs. Two miRNAs, miR-526b and miR-655, promote aggressive breast cancer phenotypes like cell proliferation, cancer stem cell upregulation, altered response to oxidative and metabolic stress and help tumor metastasis by activating COX-2/EP4/PI3K pathways. However, their impact on the effects of chemotherapeutic treatments remains unexplored. This study investigates the impact of overexpressing miR-526b and miR-655 on doxorubicin responses in breast cancer, focusing on pro-survival, apoptotic, and DNA-damage response pathways. We confirm the role of PI3K/Akt signalling in promoting cell survival and resistance </pubmed_abstract><journal>Scientific reports</journal><pagination>33584</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12480915</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Investigating the effects of miR-526b and miR-655 on doxorubicin sensitivity in breast cancer.</pubmed_title><pmcid>PMC12480915</pmcid><pubmed_authors>Opperman RM</pubmed_authors><pubmed_authors>Majumder M</pubmed_authors><pubmed_authors>Maiti S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Investigating the effects of miR-526b and miR-655 on doxorubicin sensitivity in breast cancer.</name><description>Doxorubicin is an effective treatment for breast cancer, but drug resistance poses a significant challenge. Emerging regulators of drug resistance include microRNAs, small non-coding RNAs. Two miRNAs, miR-526b and miR-655, promote aggressive breast cancer phenotypes like cell proliferation, cancer stem cell upregulation, altered response to oxidative and metabolic stress and help tumor metastasis by activating COX-2/EP4/PI3K pathways. However, their impact on the effects of chemotherapeutic treatments remains unexplored. This study investigates the impact of overexpressing miR-526b and miR-655 on doxorubicin responses in breast cancer, focusing on pro-survival, apoptotic, and DNA-damage response pathways. We confirm the role of PI3K/Akt signalling in promoting cell survival and resistance </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-07-15T09:49:49.782Z</modification><creation>2026-07-02T03:12:12.786Z</creation></dates><accession>S-EPMC12480915</accession><cross_references><pubmed>41023167</pubmed><doi>10.1038/s41598-025-18719-y</doi></cross_references></HashMap>