AI Article Synopsis

  • - Osteosarcoma is a common bone cancer affecting both kids and adults, but its development mechanisms remain largely unknown despite extensive research.
  • - Recent studies have highlighted the significant role of long noncoding RNAs (lncRNAs) in osteosarcoma, influencing its progression and invasion through various molecular signaling pathways.
  • - The review discusses specific lncRNAs, such as MALAT1 and CCAT2, that impact key signaling pathways like PI3K/Akt, Wnt/β-catenin, NF-κB, and others, suggesting potential avenues for therapeutic intervention.

Article Abstract

Osteosarcoma is one of the most commonly seen bone malignancies with high incidence rate in both children and adults. Although the regulatory network of osteosarcoma has been greatly concerned for years, the mechanisms regarding its oncogenesis and development are still not clear. Recent discoveries have revealed that long noncoding RNAs (lncRNAs) play a crucial role in the development, progression, and invasion of osteosarcoma. Deregulated expression of lncRNAs has been found to participate in the regulation of various signaling transduction pathways in osteosarcoma. This review summarized roles of lncRNAs in the pathogenesis, development, and potential therapeutic of osteosarcoma via different signaling pathways. For examples, MALAT1, CCAT2, FER1L4, LOXL1-AS1, OIP5-AS1, PVT1, DBH-AS1, and AWPPH regulate PI3K/Akt signaling; AWPPH and BE503655 regulate Wnt/β-catenin signaling; NKILA and XIST regulate NF-κB signaling; MEG3 and SNHG12 regulate Notch signaling; FOXD2-AS1 and LINK-A regulate HIF-1α signaling; GClnc1 and HOTAIR regulate P53 signaling; ZFAS1, H19, and MALAT1 regulate MAPK, Hedgehog and Rac1/JNK signaling, respectively.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307344PMC
http://dx.doi.org/10.1002/jcla.23317DOI Listing

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