LncRNA-mediated regulation of cisplatin response in breast cancer
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, přehledy
PubMed
39536542
DOI
10.1016/j.prp.2024.155716
PII: S0344-0338(24)00627-7
Knihovny.cz E-zdroje
- Klíčová slova
- Breast cancer, Cisplatin, Long non-coding RNAs, Resistance,
- MeSH
- chemorezistence * genetika MeSH
- cisplatina * terapeutické užití farmakologie MeSH
- lidé MeSH
- nádory prsu * farmakoterapie genetika patologie metabolismus MeSH
- protinádorové látky * terapeutické užití farmakologie MeSH
- regulace genové exprese u nádorů * účinky léků MeSH
- RNA dlouhá nekódující * genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- cisplatina * MeSH
- protinádorové látky * MeSH
- RNA dlouhá nekódující * MeSH
Breast cancer is a prevalent and aggressive disease characterized by high metastasis, recurrence, and mortality rates. While cisplatin is an effective chemotherapy drug, its use is limited by its toxic effects on the body. Despite advancements in therapeutic strategies, the therapeutic response is often unsatisfactory due to drug resistance, leading to poor prognosis. Recent studies have shown that cisplatin interacts with long non-coding RNAs (lncRNAs) and accelerates the development of resistance in tumor cells to therapy. This interaction highlights the complex mechanisms involved in the response of cancer cells to chemotherapy. Several lncRNAs have been identified as key players in mediating cisplatin resistance in breast cancer. These lncRNAs include SNHG15, HULC, HCP5, MT1JP, LncMat2B, DLX6-ASL, Linc00665, CARMN, and Lnc-EinRP44-3:6. These lncRNAs have been shown to target microRNAs and mRNAs and modulate the expression of genes involved in cisplatin resistance, which is important in treating breast cancer.
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