Small Molecules in the Treatment of Squamous Cell Carcinomas: Focus on Indirubins.
Mirijam SchäferMarie Luise SemmlerThoralf BernhardtTobias FischerVinodh KakkasseryRobert RamerMartin HeinSander BekeschusPeter LangerBurkhard HinzSteffen EmmertLars BoeckmannPublished in: Cancers (2021)
Skin cancers are the most common malignancies in the world. Among the most frequent skin cancer entities, squamous cell carcinoma (SCC) ranks second (~20%) after basal cell carcinoma (~77%). In early stages, a complete surgical removal of the affected tissue is carried out as standard therapy. To treat advanced and metastatic cancers, targeted therapies with small molecule inhibitors are gaining increasing attention. Small molecules are a heterogeneous group of protein regulators, which are produced by chemical synthesis or fermentation. The majority of them belong to the group of receptor tyrosine kinase inhibitors (RTKIs), which specifically bind to certain RTKs and directly influence the respective signaling pathway. Knowledge of characteristic molecular alterations in certain cancer entities, such as SCC, can help identify tumor-specific substances for targeted therapies. Most frequently, altered genes in SCC include TP53, NOTCH, EGFR, and CCND1. For example, the gene CCND1, which codes for cyclin D1 protein, is upregulated in nearly half of SCC cases and promotes proliferation of affected cells. A treatment with the small molecule 5'-nitroindirubin-monoxime (INO) leads to inhibition of cyclin D1 and thus inhibition of proliferation. As a component of Danggui Longhui Wan, a traditional Chinese medicine, indirubins are used to treat chronic diseases and have been shown to inhibit inflammatory reactions. Indirubins are pharmacologically relevant small molecules with proapoptotic and antiproliferative activity. In this review, we discuss the current literature on indirubin-based small molecules in cancer treatment. A special focus is on the molecular biology of squamous cell carcinomas, their alterations, and how these are rendered susceptible to indirubin-based small molecule inhibitors. The potential molecular mechanisms of the efficacy of indirubins in killing SCC cells will be discussed as well.
Keyphrases
- small molecule
- squamous cell
- protein protein
- signaling pathway
- induced apoptosis
- cell cycle arrest
- squamous cell carcinoma
- pi k akt
- small cell lung cancer
- skin cancer
- stem cells
- cell death
- cell cycle
- epithelial mesenchymal transition
- basal cell carcinoma
- systematic review
- binding protein
- healthcare
- genome wide
- working memory
- single molecule
- bone marrow
- high grade
- endoplasmic reticulum stress
- tyrosine kinase
- oxidative stress
- gene expression
- copy number
- combination therapy
- amino acid
- climate change
- radiation therapy