| Literature DB >> 34359854 |
Tsai-Mu Cheng1,2, Wong-Jin Chang1, Hsiu-Yi Chu1, Roberto De Luca3, Jens Z Pedersen4, Sandra Incerpi5, Zi-Lin Li6,7, Ya-Jung Shih6,7, Hung-Yun Lin7,8,9,10,11, Kuan Wang6, Jacqueline Whang-Peng7,8.
Abstract
Integrin αvβ3, a cell surface receptor, participates in signaling transduction pathways in cancer cell proliferation and metastasis. Several ligands bind to integrin αvβ3 to regulate proliferation and metastasis in cancer cells. Crosstalk between the integrin and other signal transduction pathways also plays an important role in modulating cancer proliferation. Carcinoembryonic antigen cell adhesion molecule 6 (CEACAM6) activates the downstream integrin FAK to stimulate biological activities including cancer proliferation and metastasis. Blockage of signals related to integrin αvβ3 was shown to be a promising target for cancer therapies. 3,3',5,5'-tetraiodothyroacetic acid (tetrac) completely binds to the integrin with the thyroid hormone to suppress cancer proliferation. The (E)-stilbene analog, resveratrol, also binds to integrin αvβ3 to inhibit cancer growth. Recently, nanotechnologies have been used in the biomedical field for detection and therapeutic purposes. In the current review, we show and evaluate the potentiation of the nanomaterial carrier RGD peptide, derivatives of PLGA-tetrac (NDAT), and nanoresveratrol targeting integrin αvβ3 in cancer therapies.Entities:
Keywords: NDAT; RGD; drug-delivery system; integrin αvβ3; nanomaterial; resveratrol
Year: 2021 PMID: 34359854 DOI: 10.3390/cells10071684
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600