Abstract

Simple SummaryIn this review, the genetic landscape of squamous cell carcinoma is related to the potential targets of indirubin-based small molecules in cancer therapy. Being a component of traditional Chinese medicine, indirubins are used to treat chronic or inflammatory diseases, and have received increasing attention in cancer treatment due to their proapoptotic and antiproliferative activity. Frequent genetic alterations of squamous cell carcinomas are summarized, and it is discussed how these may render tumors susceptible to indirubin-based small molecule inhibitors.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.

Highlights

  • Skin cancers are the most common malignancies in the world

  • In the ALTERNATIVE study, Lapatinib was tested in combination with the monoclonal antibody Trastuzumab (Herceptin®, Hoffmann-La Roche, Basel, Switzerland) and an aromatase inhibitor (AI) versus Trastuzumab + AI [9]

  • IMspire150 was another phase 3, randomized open-labeled study dealing with BRAF-V600-positive melanoma patients treated with Vemurafenib and the mitogen activated protein kinase (MEK)-inhibitor Cobimitinib with and without addition of the monoclonal programmed cell death ligand 1 (PD-L1) antibody Atezolizumab [32]

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Summary

Introduction

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%) [1]. Receptor tyrosine kinase (RTK) inhibitors are used to target tumor cells . Lapatinib (Tykerb®, GlaxoSmithKline, London-Brentford, UK) is such an inhibitor targeting the receptor tyrosine kinase and EGFR-member ErbB2 to treat breast cancer (BC). Indirubins have been shown to inhibit DNA synthesis, protein kinases [17,18,19], and cyclin-dependent kinases [19] They intervene directly with signaling pathways frequently altered in cancer cells and, have the potential to prevent tumor cell proliferation and augment cytotoxicity. We discuss the current literature on indirubin-based small molecules in cancer treatment. A particular focus is on the molecular biology of squamous cell carcinomas, their alterations, and how this may render these tumors susceptible to indirubin-based small molecule inhibitors. Potential molecular mechanisms of indirubins-induced toxicity in cancer cells will be discussed

Small Molecules
Mode of Action of Small Molecules and Potential Targets in Cancer
Background
Molecular Biology of Squamous Cell Carcinoma
Small Molecules Based on Indirubins in the Treatment of SCC
Findings
Conclusions
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