CAIX-Mediated Control of LIN28/let-7 Axis Contributes to Metabolic Adaptation of Breast Cancer Cells to Hypoxia
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
14-0816
Agentúra na Podporu Výskumu a Vývoja
15-0697
Agentúra na Podporu Výskumu a Vývoja
2/0155/15
Vedecká Grantová Agentúra MŠVVaŠ SR a SAV
2/0076/20
Vedecká Grantová Agentúra MŠVVaŠ SR a SAV
2/0105/19
Vedecká Grantová Agentúra MŠVVaŠ SR a SAV
PubMed
32560271
PubMed Central
PMC7352761
DOI
10.3390/ijms21124299
PII: ijms21124299
Knihovny.cz E-zdroje
- Klíčová slova
- LIN28/let-7 axis, carbonic anhydrase IX, hypoxia, metabolism,
- MeSH
- antigeny nádorové genetika MeSH
- glykolýza MeSH
- hypoxie buňky MeSH
- karboanhydrasa IX genetika MeSH
- koncentrace vodíkových iontů MeSH
- lidé MeSH
- MFC-7 buňky MeSH
- mikro RNA genetika MeSH
- nádorové buněčné linie MeSH
- nádorové kmenové buňky metabolismus MeSH
- nádory prsu genetika metabolismus MeSH
- přeprogramování buněk MeSH
- proteiny vázající RNA genetika MeSH
- stanovení celkové genové exprese MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigeny nádorové MeSH
- CA9 protein, human MeSH Prohlížeč
- karboanhydrasa IX MeSH
- Lin28A protein, human MeSH Prohlížeč
- mikro RNA MeSH
- mirnlet7 microRNA, human MeSH Prohlížeč
- proteiny vázající RNA MeSH
Solid tumors, including breast cancer, are characterized by the hypoxic microenvironment, extracellular acidosis, and chemoresistance. Hypoxia marker, carbonic anhydrase IX (CAIX), is a pH regulator providing a selective survival advantage to cancer cells through intracellular neutralization while facilitating tumor invasion by extracellular acidification. The expression of CAIX in breast cancer patients is associated with poor prognosis and metastases. Importantly, CAIX-positive hypoxic tumor regions are enriched in cancer stem cells (CSCs). Here we investigated the biological effects of CA9-silencing in breast cancer cell lines. We found that CAIX-downregulation in hypoxia led to increased levels of let-7 (lethal-7) family members. Simultaneously with the increase of let-7 miRNAs in CAIX-suppressed cells, LIN28 protein levels decreased, along with downstream metabolic pathways: pyruvate dehydrogenase kinase 1 (PDK1) and phosphorylation of its substrate, pyruvate dehydrogenase (PDH) at Ser-232, causing attenuation of glycolysis. In addition to perturbed glycolysis, CAIX-knockouts, in correlation with decreased LIN28 (as CSC reprogramming factor), also exhibit reduction of the further CSC-associated markers NANOG (Homeobox protein NANOG) and ALDH1 (Aldehyde dehydrogenase isoform 1). Oppositely, overexpression of CAIX leads to the enhancement of LIN28, ALDH1, and NANOG. In conclusion, CAIX-driven regulation of the LIN28/let-7 axis augments glycolytic metabolism and enhances stem cell markers expression during CAIX-mediated adaptation to hypoxia and acidosis in carcinogenesis.
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