| Literature DB >> 34249465 |
Yoshihisa Tokumaru1,2, Masanori Oshi1,3, Ankit Patel1, Eriko Katsuta1, Li Yan4, Fernando A Angarita1, Subhamoy Dasgupta5, Masayuki Nagahashi6, Nobuhisa Matsuhashi2, Manabu Futamura2, Kazuhiro Yoshida2, Kazuaki Takabe1,3,6,7,8,9.
Abstract
MiR-195 is a tumor suppressive microRNA in breast cancer. Its clinical relevance remains debatable as it has only been studied via in vitro experiments or small cohort studies. We analyzed a total of 2,038 patients in the TCGA and METABRIC cohorts to assess whether low miR-195 expressing tumors are associated with aggressive cancer characteristics and poor prognostic outcomes. The median cutoff of miR-195 expression was used to split the groups into miR-195 high and low groups. Low miR-19 expressing tumors demonstrated high cell proliferating features by enriching the gene sets associated with cell proliferation, MKI67 expression and pathological grade. One-third of the top target miR-195 genes were related to cell proliferation. Low miR-195 expressing tumors were associated with both pro-cancerous and anti-cancerous immune cells. Low miR-195 expressing tumors were associated with enhanced glycolysis and poor survival in ER-positive tumors, but not other subtypes of breast cancer. In conclusion, low expression of miR-195 in ER-positive breast cancer was associated with enhanced cancer cell proliferation, glycolysis, and worse overall survival. AJCREntities:
Keywords: GSEA; METABRIC; MicroRNA; TCGA; breast cancer; cell proliferation; glycolysis; miR-195
Year: 2021 PMID: 34249465 PMCID: PMC8263660
Source DB: PubMed Journal: Am J Cancer Res ISSN: 2156-6976 Impact factor: 6.166