The Role of IGF/IGF-1R Signaling in Hepatocellular Carcinomas: Stemness-Related Properties and Drug Resistance.
Mai-Huong Thi NgoHan-Yin JengYung-Che KuoJosephine Diony NandaAgeng BrahmadhiThai-Yen LingTe-Sheng ChangYen-Hua HuangPublished in: International journal of molecular sciences (2021)
Insulin-like Growth Factor (IGF)/IGF-1 Receptor (IGF-1R) signaling is known to regulate stem cell pluripotency and differentiation to trigger cell proliferation, organ development, and tissue regeneration during embryonic development. Unbalanced IGF/IGF-1R signaling can promote cancer cell proliferation and activate cancer reprogramming in tumor tissues, especially in the liver. Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death, with a high incidence and mortality rate in Asia. Most patients with advanced HCC develop tyrosine kinase inhibitor (TKI)-refractoriness after receiving TKI treatment. Dysregulation of IGF/IGF-1R signaling in HCC may activate expression of cancer stemness that leads to TKI refractoriness and tumor recurrence. In this review, we summarize the evidence for dysregulated IGF/IGF-1R signaling especially in hepatitis B virus (HBV)-associated HCC. The regulation of cancer stemness expression and drug resistance will be highlighted. Current clinical treatments and potential therapies targeting IGF/IGF-1R signaling for the treatment of HCC will be discussed.
Keyphrases
- binding protein
- pi k akt
- stem cells
- growth hormone
- hepatitis b virus
- cell proliferation
- papillary thyroid
- signaling pathway
- poor prognosis
- squamous cell
- gene expression
- tyrosine kinase
- epithelial mesenchymal transition
- drug delivery
- cell cycle
- lymph node metastasis
- mesenchymal stem cells
- risk factors
- squamous cell carcinoma
- liver failure
- childhood cancer
- human health