Role of thyroid hormone-integrin αvβ3-signal and therapeutic strategies in colorectal cancers.
Yu-Chen S H YangPo-Jui KoYi-Shin PanHung-Yun LinJacqueline Whang-PengPaul J DavisKuan WangPublished in: Journal of biomedical science (2021)
Thyroid hormone analogues-particularly, L-thyroxine (T4) has been shown to be relevant to the functions of a variety of cancers. Integrin αvβ3 is a plasma membrane structural protein linked to signal transduction pathways that are critical to cancer cell proliferation and metastasis. Thyroid hormones, T4 and to a less extend T3 bind cell surface integrin αvβ3, to stimulate the extracellular signal-regulated kinase 1/2 (ERK1/2) pathway to stimulate cancer cell growth. Thyroid hormone analogues also engage in crosstalk with the epidermal growth factor receptor (EGFR)-Ras pathway. EGFR signal generation and, downstream, transduction of Ras/Raf pathway signals contribute importantly to tumor cell progression. Mutated Ras oncogenes contribute to chemoresistance in colorectal carcinoma (CRC); chemoresistance may depend in part on the activity of ERK1/2 pathway. In this review, we evaluate the contribution of thyroxine interacting with integrin αvβ3 and crosstalking with EGFR/Ras signaling pathway non-genomically in CRC proliferation. Tetraiodothyroacetic acid (tetrac), the deaminated analogue of T4, and its nano-derivative, NDAT, have anticancer functions, with effectiveness against CRC and other tumors. In Ras-mutant CRC cells, tetrac derivatives may overcome chemoresistance to other drugs via actions initiated at integrin αvβ3 and involving, downstream, the EGFR-Ras signaling pathways.
Keyphrases
- epidermal growth factor receptor
- wild type
- signaling pathway
- tyrosine kinase
- pi k akt
- induced apoptosis
- small cell lung cancer
- cell proliferation
- advanced non small cell lung cancer
- papillary thyroid
- cell cycle arrest
- cell migration
- cell surface
- epithelial mesenchymal transition
- cell adhesion
- molecular docking
- transcription factor
- squamous cell carcinoma
- binding protein
- single cell
- stem cells
- systematic review
- mesenchymal stem cells
- young adults
- cell death
- drug induced