Contribution of LAT1-4F2hc in Urological Cancers via Toll-like Receptor and Other Vital Pathways.
Xue ZhaoShinichi SakamotoMaihulan MaimaitiNaohiko AnzaiTomohiko IchikawaPublished in: Cancers (2022)
Tumor cells are known for their ability to proliferate. Nutrients are essential for rapidly growing tumor cells. In particular, essential amino acids are essential for tumor cell growth. Tumor cell growth nutrition requires the regulation of membrane transport proteins. Nutritional processes require amino acid uptake across the cell membrane. Leucine, one of the essential amino acids, has recently been found to be closely associated with cancer, which activate mTOR signaling pathway. The transport of leucine into cells requires an L-type amino acid transporter protein 1, LAT1 (SLC7A5), which requires the 4F2 cell surface antigen heavy chain (4F2hc, SLC3A2) to form a heterodimeric amino acid transporter protein complex. Recent evidence identified 4F2hc as a specific downstream target of the androgen receptor splice variant 7 (AR-V7). We stressed the importance of the LAT1-4F2hc complex as a diagnostic and therapeutic target in urological cancers in this review, which covered the recent achievements in research on the involvement of the LAT1-4F2hc complex in urinary system tumors. In addition, JPH203, which is a selective LAT1 inhibitor, has shown excellent inhibitory effects on the proliferation in a variety of tumor cells. The current phase I clinical trials of JPH203 in patients with biliary tract cancer have also achieved good results, which is the future research direction for LAT1 targeted therapy drugs.
Keyphrases
- amino acid
- toll like receptor
- signaling pathway
- papillary thyroid
- clinical trial
- induced apoptosis
- cell surface
- inflammatory response
- squamous cell
- pi k akt
- immune response
- nuclear factor
- cell cycle arrest
- physical activity
- cell proliferation
- childhood cancer
- epithelial mesenchymal transition
- oxidative stress
- heavy metals
- randomized controlled trial
- small molecule
- binding protein
- endoplasmic reticulum stress
- protein protein