AI Article Synopsis

  • * The Shh pathway is activated when its ligands bind to the Ptch receptor, leading to the activation of key signaling components that contribute to HCC progression, with overexpression of these molecules observed in HCC patients.
  • * Inhibiting the Shh signaling pathway shows promise in reducing HCC growth, enhancing sensitivity to radiation, and improving chemotherapy effectiveness, suggesting it could be a valuable target for HCC treatment.

Article Abstract

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-associated mortality worldwide. Hepatocarcinogenesis involves numerous interlinked factors and processes, including the Sonic hedgehog (Shh) signaling pathway, which participates in the carcinogenesis, progression, invasiveness, recurrence and cancer stem cell maintenance of HCC. The Shh signaling pathway is activated by ligands that bind to their receptor protein, Protein patched homolog (Ptch). The process of Shh ligand binding to Ptch weakens the inhibition of smoothened homolog (SMO) and activates signal transduction via glioma-associated oncogene homolog (Gli) transcription factors. The overexpression of Shh pathway molecules, including Shh, Ptch-1, Gli and SMO has been indicated in patients with HCC. It has also been suggested that the Shh signaling pathway exhibits cross-talk between numerous other signaling pathways. The inactivation of the Shh signaling pathway reduces HCC growth, increases radio-sensitivity and increases the beneficial effect of chemotherapy in HCC treatment. Therefore, inhibition of the Shh pathway may be an effective target therapy that can be used in the treatment of HCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781692PMC
http://dx.doi.org/10.3892/ol.2019.10826DOI Listing

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