Advancements in Utilizing Natural Compounds for Modulating Autophagy in Liver Cancer: Molecular Mechanisms and Therapeutic Targets.
Md Ataur RahmanS M Rakib-Uz-ZamanSomdeepa ChakrabortiSujay Kumar BhajanRajat Das GuptaMaroua JalouliMd Anowar Khasru ParvezMushfiq Hassan ShaikhEhsanul Hoque ApuAbdel Halim HarrathSeungjoon MoonBonlgee KimPublished in: Cells (2024)
Autophagy, an intrinsic catabolic mechanism that eliminates misfolded proteins, dysfunctional organelles, and lipid droplets, plays a vital function in energy balance and cytoplasmic quality control, in addition to maintaining cellular homeostasis. Liver cancer such as hepatocellular carcinoma (HCC) is one of the most common causes of cancer deaths globally and shows resistance to several anticancer drugs. Despite the rising incidence and poor prognosis of malignant HCC, the underlying molecular mechanisms driving this aggressive cancer remain unclear. Several natural compounds, such as phytochemicals of dietary and non-dietary origin, affect hepatocarcinogenesis signaling pathways in vitro and in vivo, which may help prevent and treat HCC cells. Current HCC cells treatments include chemotherapy, radiation, and surgery. However, these standard therapies have substantial side effects, and combination therapy enhances side effects for an acceptable therapeutic benefit. Therefore, there is a need to develop treatment strategies for HCC cells that are more efficacious and have fewer adverse effects. Multiple genetic and epigenetic factors are responsible for the HCC cells to become resistant to standard treatment. Autophagy contributes to maintain cellular homeostasis, which activates autophagy for biosynthesis and mitochondrial regulation and recycling. Therefore, modifying autophagic signaling would present a promising opportunity to identify novel therapies to treat HCC cells resistant to current standard treatments. This comprehensive review illustrates how natural compounds demonstrate their anti-hepatocellular carcinoma function through autophagy.
Keyphrases
- induced apoptosis
- cell death
- cell cycle arrest
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- poor prognosis
- combination therapy
- long non coding rna
- epithelial mesenchymal transition
- radiation therapy
- pi k akt
- gene expression
- quality control
- coronary artery disease
- cell proliferation
- fatty acid
- radiation induced
- atrial fibrillation
- copy number